The Turkish Journal of Pediatrics
Smilar Issues: 292 Record Found
The Fanconi syndrome of cystinosis: insights into the pathophysiology Abstract Similar Articles Mail to Editor Childhood onset of narcolepsy-cataplexy syndrome in Turkey: clinical and genetic study Abstract Similar Articles Mail to Editor Munchausen syndrome by proxy: a case report Abstract Similar Articles Mail to Editor Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome Abstract Similar Articles Mail to Editor Tropical pediatrics: 2002 to 2015 Abstract Similar Articles Mail to Editor A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts Abstract Similar Articles Mail to Editor Bardet-Biedl syndrome associated with vaginal atresia: a case report Abstract Similar Articles Mail to Editor Short rib-polydactyly syndrome: a case report Abstract Similar Articles Mail to Editor Horner's syndrome secondary to tube thoracostomy Abstract Similar Articles Mail to Editor Prenatal diagnosis of Meckel-Gruber syndrome and Dandy-Walker malformation in four consecutive affected siblings, with the fourth one being diagnosed prenatally at 22 weeks of gestation Abstract Similar Articles Mail to Editor Hypercalciuria and nephrocalcinosis in cystic fibrosis patients Abstract Similar Articles Mail to Editor Absent pulmonary valve syndrome diagnosed by fetal echocardiography Abstract Similar Articles Mail to Editor Pediatric cerebellar cystic oligodendroglioma: case report and literature review Abstract Similar Articles Mail to Editor Albert Eckstein: a pioneer in pediatrics in Turkey Abstract Similar Articles Mail to Editor PFAPA syndrome: a rare cause of periodic fever Abstract Similar Articles Mail to Editor LEOPARD syndrome and hypertrophic obstructive cardiomyopathy: a case report Abstract Similar Articles Mail to Editor Meckel-Gruber syndrome associated with gastrointestinal tractus anomaly Abstract Similar Articles Mail to Editor A case with ICF syndrome lost to rubella pneumonitis Abstract Similar Articles Mail to Editor Raine syndrome associated with cytomegalovirus infection Abstract Similar Articles Mail to Editor Magnetic resonance angiographic and three-dimensional computerized tomographic identification of scimitar syndrome in an 8-month-old infant Abstract Similar Articles Mail to Editor Celiac disease screening in 100 Turkish children with Down syndrome Abstract Similar Articles Mail to Editor Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations Abstract Similar Articles Mail to Editor Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome Abstract Similar Articles Mail to Editor Visceral leishmaniasis and pseudomonas septicemia associated with hemophagocytic syndrome and myelodysplasia in a Turkish child Abstract Similar Articles Mail to Editor Childhood mediastinal masses in infants and children Abstract Similar Articles Mail to Editor A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4 Abstract Similar Articles Mail to Editor A very rare case of polysplenia syndrome with congenital diffuse pulmonary arteriovenous fistulas Abstract Similar Articles Mail to Editor Propylthiouracil-induced hypersensitivity syndrome Abstract Similar Articles Mail to Editor Steroid-induced psychosis in an adolescent: treatment and prophylaxis with risperidone Abstract Similar Articles Mail to Editor A patient with cystinosis presenting transient features of Bartter syndrome Abstract Similar Articles Mail to Editor A 13-year-old female with Turner syndrome and achalasia Abstract Similar Articles Mail to Editor Factors influencing outcome of inpatient pediatric resuscitation Abstract Similar Articles Mail to Editor Mechanical ventilation in children Abstract Similar Articles Mail to Editor DMSA findings in the evaluation of pediatric renal allograft Abstract Similar Articles Mail to Editor Parvovirus B19 associated papular-purpuric gloves-and-socks syndrome Abstract Similar Articles Mail to Editor Tracheobronchial calcification associated with Keutel syndrome Abstract Similar Articles Mail to Editor Effective treatment of multifocal aggressive fibromatosis with low-dose chemotherapy Abstract Similar Articles Mail to Editor Genetic factors in neonatal hyperbilirubinemia and kernicterus Abstract Similar Articles Mail to Editor Co-infection with Mycoplasma pneumoniae and cytomegalovirus resulting in an acute demyelinating polyneuropathy in a pediatric patient Abstract Similar Articles Mail to Editor Acute purulent meningitis associated with chronic subdural hematoma and subdural hygroma Abstract Similar Articles Mail to Editor Axenfeld-Rieger syndrome associated with truncus arteriosus: a case report Abstract Similar Articles Mail to Editor A survey of pediatric intensive care services in Turkey Abstract Similar Articles Mail to Editor Assessment of quality of life in asthmatic Turkish children Abstract Similar Articles Mail to Editor Familial Mediterranean fever in northwest of Iran (Ardabil): the first global report from Iran Abstract Similar Articles Mail to Editor A rare form of Guillain-Barré syndrome: pharyngeal-cervical-brachial variant Abstract Similar Articles Mail to Editor Genetic dilemma: eNOS gene intron 4a/b VNTR polymorphism in sepsis and its clinical features in Turkish children Abstract Similar Articles Mail to Editor Angelman syndrome: clinical findings and follow-up data of 14 patients Abstract Similar Articles Mail to Editor A study of perceptions, attitudes, and level of knowledge among pediatricians towards attention-deficit/hyperactivity disorder Abstract Similar Articles Mail to Editor The Incidence of Congenital Malformations in Children with Cancer Abstract Similar Articles Mail to Editor The Impact of Pediatric Trauma Score on Burden of Trauma in Emergency Room Care Abstract Similar Articles Mail to Editor Validation and Reliability Study of the Turkish Version of the Pediatric Rhinitis Quality of Life Questionnaire Abstract Similar Articles Mail to Editor Burn Injuries Among Children Aged Up To Seven Years Abstract Similar Articles Mail to Editor The Relationship Between Group A Beta Hemolytic Streptococcal Infection and Psychiatric Symptoms: A Pilot Study Abstract Similar Articles Mail to Editor Double Outlet Right Ventricle with Giant Pulmonary Artery Aneurysm and Severe Aortic Coarctation: Diagnosis with Multislice CT Abstract Similar Articles Mail to Editor Baboon Syndrome and Segmental Vitiligo Coexistence Abstract Similar Articles Mail to Editor Plummer-Vinson Syndrome in a 15-Year-Old Boy Abstract Similar Articles Mail to Editor Purpura Fulminans as the Presenting Manifestation in a Patient with Juvenile SLE Abstract Similar Articles Mail to Editor Precocious Puberty in a Girl with Down Syndrome due to Primary Hypothyroidism Abstract Similar Articles Mail to Editor Kabuki make-up syndrome with unilateral renal agenesis Abstract Similar Articles Mail to Editor Pediatric pleural effusions: etiological evaluation in 492 patients over 29 years Abstract Similar Articles Mail to Editor Subtelomeric Rearrangements in Mental Retardation: Hacettepe University Abstract Similar Articles Mail to Editor A report of a patient with duplication of 7p13→pter and deletion of 2p23→pter due to a maternal 2p;7p translocation Abstract Similar Articles Mail to Editor A novel mutation of the GLUT2 gene in a Turkish patient with Fanconi-Bickel syndrome Abstract Similar Articles Mail to Editor Management of central diabetes insipidus with oral desmopressin in a patient with ectrodactyly and cleft lip/palate (ECP) syndrome Abstract Similar Articles Mail to Editor Antiepileptic hypersensitivity and DRESS syndrome due to phenytoin in two pediatric cases Abstract Similar Articles Mail to Editor Successful treatment with gemtuzumab ozogamicin monotherapy in a pediatric patient with resistant relapse of acute myeloid leukemia Abstract Similar Articles Mail to Editor Pediatricians’ knowledge about recent advances in anaphylaxis treatment in İstanbul, Turkey Abstract Similar Articles Mail to Editor A well-documented trisomy 13 case presenting with a number of common and uncommon features of the syndrome Abstract Similar Articles Mail to Editor Two new cases with Pearson syndrome and review of Hacettepe experience Abstract Similar Articles Mail to Editor The absence of peripheral blood blasts at diagnosis may predict CNS involvement or CNS relapse in pediatric acute lymphoblastic leukemia patients Abstract Similar Articles Mail to Editor The prognostic impact of myeloid antigen expression in pediatric acute lymphoblastic leukemia patients Abstract Similar Articles Mail to Editor Desmoplastic infantile ganglioglioma: case report Abstract Similar Articles Mail to Editor Metabolic syndrome in obese Turkish children and adolescents: comparison of two diagnostic models Abstract Similar Articles Mail to Editor Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: a case report Abstract Similar Articles Mail to Editor Approach in an adolescent Proteus male patient with megafoot Abstract Similar Articles Mail to Editor A case with a ring chromosome 22 Abstract Similar Articles Mail to Editor Aplasia Cutis Congenita: Three Cases with Three Different Underlying Etiologies Abstract Similar Articles Mail to Editor Early administration of the second surfactant dose in preterm infants with severe respiratory distress syndrome Abstract Similar Articles Mail to Editor 3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures Abstract Similar Articles Mail to Editor Acquired partial lipodystrophy associated with varicella Abstract Similar Articles Mail to Editor Fetal sodium valproate exposure causes Baller-Gerold syndrome phenotype: both phenotypes in the same family Abstract Similar Articles Mail to Editor Nosocomial transmission of Candida pelliculosa fungemia in a pediatric intensive care unit and review of the literature Abstract Similar Articles Mail to Editor A Case of Late-Onset Central Hypoventilation Syndrome with Hypothalamic Dysfunction: Through a New Phenotype Abstract Similar Articles Mail to Editor A Turner Syndrome Case Associated with Anal Atresia, Interrupted Aortic Arch and Multicystic Dysplastic Kidney Abstract Similar Articles Mail to Editor Anti-GQ1b-Negative Miller Fisher Syndrome Presented with One-Sided Horizontal Gaze Palsy Abstract Similar Articles Mail to Editor A Mother and Son with Noonan Syndrome Resulting from a PTPN11 Mutation: First Report of Molecularly Proven Cases from Turkey Abstract Similar Articles Mail to Editor Cowden Syndrome with Bronchial Asthma Abstract Similar Articles Mail to Editor Quadricuspid Aortic Valve Diagnosed by Transthoracic Echocardiography in Childhood Abstract Similar Articles Mail to Editor Pseudotumor Cerebri in a Child with Hyperimmunoglobulin E Syndrome Abstract Similar Articles Mail to Editor A Novel Mutation İn The DGUOK Gene İn A Turkish Newborn With Mitochondrial Depletion Syndrome Abstract Similar Articles Mail to Editor A Challenging Review Of Childhood İncontinence: Rare Complications Of Dysfunctional Elimination Syndrome İn An Epileptic Boy Abstract Similar Articles Mail to Editor Cardiovascular Findings İn A Boy With Arterial Tortuosity Syndrome: Case Report And Review Of The Literature Abstract Similar Articles Mail to Editor Nosocomial Infections Due to Acinetobacter Baumannii in A Pediatric Intensive Care Unit in Turkey Abstract Similar Articles Mail to Editor Hospitalizations for Pediatric Intoxication: A Study from İstanbul Abstract Similar Articles Mail to Editor Giant Mesenteric Cyst of Gastric Origin: A Case Report with Imaging Findings Abstract Similar Articles Mail to Editor Two Sisters with Bardet-Biedl Syndrome: Brain Abnormalities and Unusual Facial Findings Abstract Similar Articles Mail to Editor Pediatric Tracheotomy: 3-Year Experience at a Tertiary Care Center with 54 Children Abstract Similar Articles Mail to Editor Suppurative Cervical Adenopathy and Pharyngeal Mass due to Tularemia Unresponsive to Medical Treatment Abstract Similar Articles Mail to Editor Postinfarction Ventricular Septal Defect Following Blunt Chest Trauma in a 7-Year-Old Child Abstract Similar Articles Mail to Editor Conus Medullaris Syndrome and Acute Colonic Pseudo-Obstruction in a Child with Acute Lymphoblastic Leukemia Abstract Similar Articles Mail to Editor Assessment of Bone Density in Children with Cerebral Palsy by Areal Bone Mineral Density Measurement Abstract Similar Articles Mail to Editor Two Cases of LEOPARD Syndrome – RAF1 Mutations Firstly Described in Children Abstract Similar Articles Mail to Editor Hypopituitarism Masquerading as Prasad’s Syndrome: A Case Report Abstract Similar Articles Mail to Editor Sjögren-Larsson Syndrome: Report of Monozygote Twins and a Case with a Novel Mutation Abstract Similar Articles Mail to Editor Prenatally Diagnosed Case of 22q11.2 Deletion Syndrome Associated with Pulmonary Artery Aneurysm Abstract Similar Articles Mail to Editor Cardiogenic Shock: Do Not Forget the Possibility of Kawasaki Disease Abstract Similar Articles Mail to Editor Incidence and Risk Factors for Retinopathy of Prematurity in the West Black Sea Region, Turkey Abstract Similar Articles Mail to Editor Papillon-Lefèvre Syndrome: Report of Three Cases in the Same Family Abstract Similar Articles Mail to Editor Arterial Tortuosity and Aneurysm in a Case of Loeys-Dietz Syndrome Type IB with a Mutation p.R537P in the TGFBR2 Gene Abstract Similar Articles Mail to Editor Toxicological Evaluation of Two Children Diagnosed as Munchausen Syndrome by Proxy Abstract Similar Articles Mail to Editor Catheter Fragment Embolization: A Rare Yet Serious Complication of Catheter Use in Pediatric Oncology Abstract Similar Articles Mail to Editor Is there a necessity for multiple doses of surfactant for respiratory distress syndrome of premature infants? Abstract Similar Articles Mail to Editor Two newborns of heroin-addicted mothers suffering neonatal withdrawal syndrome Abstract Similar Articles Mail to Editor Malignant melanoma developed on a congenital melanocytic nevus with lymph node metastasis in a 19-month-old boy Abstract Similar Articles Mail to Editor Complications of Cardiac Catheterization in Pediatric Patients: a Single Center Experience Abstract Similar Articles Mail to Editor Pediatric Tracheotomy: Comparison of Indications and Complications between Children and Adults Abstract Similar Articles Mail to Editor Congenital Central Hypoventilation Syndrome with Hirschsprung’s Disease due to PHOX2B Gene Mutation in a Turkish Infant Abstract Similar Articles Mail to Editor A Case of Mowat-Wilson Syndrome Caused by a Truncating Mutation within Exon 8 of the ZEB2 Gene Abstract Similar Articles Mail to Editor Bilateral Pheochromocytoma as First Manifestation of von Hippel-Lindau Disease: A Case Report Abstract Similar Articles Mail to Editor The MEFV gene and clonal myeloid disorders Abstract Similar Articles Mail to Editor Frequency of Mutations in PROP-1 Gene in Turkish Children with Combined Pituitary Hormone Deficiency Abstract Similar Articles Mail to Editor Joubert Syndrome: Report of 11 Cases Abstract Similar Articles Mail to Editor Randomized Controlled Trial of Two Methods of Nasal Continuous Positive Airway Pressure (N-CPAP) in Preterm Infants with Respiratory Distress Syndrome: Underwater Bubbly CPAP vs. Medijet System Device Abstract Similar Articles Mail to Editor Mevalonate Kinase Deficiency (Hyper IgD Syndrome with Periodic Fever) - Different Faces with Separate Treatments: Two Cases and Review of the Literature Abstract Similar Articles Mail to Editor Different Presentations in Patients with Tumor Necrosis Factor Receptor-Associated Periodic Syndrome Mutations: Report of Two Cases Abstract Similar Articles Mail to Editor A Novel OCRL1 Gene Mutation in a Turkish Child with Lowe Syndrome Abstract Similar Articles Mail to Editor Atypical Hemolytic Uremic Syndrome due to Factor H Autoantibody Abstract Similar Articles Mail to Editor An Unusual Cause of Secondary Capillary Leak Syndrome in a Child: Rotavirus Diarrhea Abstract Similar Articles Mail to Editor Infectious Complications and Conservative Treatment of Totally Implantable Venous Access Devices in Children with Cancer Abstract Similar Articles Mail to Editor Jacobsen Syndrome without Thrombocytopenia: A Case Report and Review of the Literature Abstract Similar Articles Mail to Editor A Case of Sotos Syndrome with 5q35 Microdeletion and Novel Clinical Findings Abstract Similar Articles Mail to Editor Bart’s Syndrome Associated with Pyloric and Choanal Atresia Abstract Similar Articles Mail to Editor Hemolytic Uremic Syndrome Outbreak in Turkey in 2011 Abstract Similar Articles Mail to Editor Diagnostic Dilemma in Autoinflammatory Disease in Two Patients: Does the Name Matter? Abstract Similar Articles Mail to Editor Kawasaki Disease Shock Syndrome: A Severe Form of Kawasaki Disease Abstract Similar Articles Mail to Editor Selective Proximal Renal Tubular Involvement and Dyslipidemia in Two Cousins with Oculocerebrorenal Syndrome of Lowe Abstract Similar Articles Mail to Editor Munchausen Syndrome by Proxy Presented as Recurrent Respiratory Arrest and Thigh Abscess: A Case Study and Overview Abstract Similar Articles Mail to Editor Neurophysiological Follow-Up of Two Siblings with Crigler-Najjar Syndrome Type I and Review of Literature Abstract Similar Articles Mail to Editor A life-threatening respiratory syncytial virus infection: a previously healthy infant with bilateral spontaneous pneumothorax and acute respiratory distress syndrome Abstract Similar Articles Mail to Editor Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report Abstract Similar Articles Mail to Editor Anesthesia for percutaneous transcatheter closure of atrial and ventricular septal defects in pediatric patients Abstract Similar Articles Mail to Editor The first case of Bruck syndrome associated with gastroschisis Abstract Similar Articles Mail to Editor Association of respiratory distress syndrome and perinatal hypoxia with histologic chorioamnionitis in preterm infants Abstract Similar Articles Mail to Editor Atypical Fryns syndrome: clinical, radiological and pathological findings Abstract Similar Articles Mail to Editor Celiac Disease in Williams-Beuren Syndrome Abstract Similar Articles Mail to Editor The Significance of Molecular Studies in the Long-Term Follow-Up of Children with Beckwith- Wiedemann Syndrome Abstract Similar Articles Mail to Editor Distribution of Pediatric Bone and Soft Tissue Tumors in the Central Black Sea Region Abstract Similar Articles Mail to Editor INSURE Method (INtubation-SURfactant-Extubation) in Early and Late Premature Neonates with Respiratory Distress: Factors Affecting the Outcome and Survival Rate Abstract Similar Articles Mail to Editor Deep Neck Infections in Children: Experience in a Tertiary Care Center in Turkey Abstract Similar Articles Mail to Editor Cross-Reactivity Syndromes: Presentation of Two Cases and Review of the Literature Abstract Similar Articles Mail to Editor Solid Pseudopapillary Tumor of the Pancreas: A Rare Entity Abstract Similar Articles Mail to Editor The X Chromosome: Does It Have a Role in Bloom Syndrome, a Genomic Instability Disorder? Abstract Similar Articles Mail to Editor An Uncommon Disorder with Multiple Skeletal Anomalies: Gorlin-Goltz Syndrome Abstract Similar Articles Mail to Editor Development of End-Stage Renal Disease at a Young Age in Two Cases with Joubert Syndrome Abstract Similar Articles Mail to Editor Neonate Born to Hepatitis B Carrier Mother Presenting with Congenital Onychodysplasia of the Index Finger (Iso–Kikuchi Syndrome) Abstract Similar Articles Mail to Editor Controversy Regarding Paracetamol- and Codeine Phosphate-Induced Acute Tubulointerstitial Nephritis-Uveitis (TINU) Syndrome Abstract Similar Articles Mail to Editor Neuroleptic Malignant Syndrome Associated with Metoclopramide in a Child Abstract Similar Articles Mail to Editor Jervell and Lange-Nielsen Syndrome with Homozygous Missense Mutation of the KCNQ1 Gene Abstract Similar Articles Mail to Editor Bilateral Congenital Cataracts in an Infant with Klinefelter Syndrome Abstract Similar Articles Mail to Editor Traumatic Multiple Lower Cranial Nerve Palsy: A Case Report and Review of the Literature Abstract Similar Articles Mail to Editor Brain Death and Organ Donation of Children Abstract Similar Articles Mail to Editor Prevalence of Irritable Bowel Syndrome in Adolescents in Turkey: Effects of Gender, Lifestyle and Psychological Factors Abstract Similar Articles Mail to Editor Refusal of Medical Treatment in the Pediatric Emergency Service: Analysis of Reasons and Aspects Abstract Similar Articles Mail to Editor Middle Aortic Syndrome in a Teenager Abstract Similar Articles Mail to Editor Crescentic Glomerulonephritis in a Child with Heiner Syndrome Abstract Similar Articles Mail to Editor A Newborn with Pertussis Accompanying Nephrotic Syndrome Abstract Similar Articles Mail to Editor Early or Later Prophylactic INSURE in Preterm Infants of Less Than 30 Weeks’ Gestation Abstract Similar Articles Mail to Editor Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation Abstract Similar Articles Mail to Editor Hypersensitivity pneumonia in a schoolchild admitted to the hospital’s asthma clinic Abstract Similar Articles Mail to Editor DRESS Syndrome Presents as Leukoencephalopathy Abstract Similar Articles Mail to Editor An antenatal appearance of megacystis-microcolon-intestinal hypoperistalsis syndrome Abstract Similar Articles Mail to Editor Tetralogy of Fallot and hypertrophic cardiomyopathy in a case of cardiofaciocutaneous syndrome Abstract Similar Articles Mail to Editor Gianotti-Crosti syndrome as the only manifestation of primary Epstein-Barr virus infection: a case report Abstract Similar Articles Mail to Editor Childhood injuries in Tehran: a review of 1281 cases Abstract Similar Articles Mail to Editor Hyperprostaglandin E syndrome: use of indomethacin and steroid, and death due to necrotizing enterocolitis and sepsis Abstract Similar Articles Mail to Editor A case of postganglionic Horner syndrome after catheterization of internal jugular vein confirmed with pharmacological tests Abstract Similar Articles Mail to Editor Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue Abstract Similar Articles Mail to Editor Adult height in Turkish patients with Turner syndrome without growth hormone treatment Abstract Similar Articles Mail to Editor Association of Campylobacter jejuni infection and Guillain- Barré syndrome: a cohort study in the northwest of Iran Abstract Similar Articles Mail to Editor Enterohemorrhagic Escherichia coli O157:H7: case report Abstract Similar Articles Mail to Editor Kidney stone and urinary bladder telangiectasia in a patient with TAR syndrome Abstract Similar Articles Mail to Editor A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns Abstract Similar Articles Mail to Editor An unusual presentation of cardiomyopathy in a patient with microcephaly-cardiomyopathy syndrome Abstract Similar Articles Mail to Editor Novel Nonsense Mutation of GPC3 Gene in a Patient with Simpson-Golabi-Behmel Syndrome Abstract Similar Articles Mail to Editor The EEC Syndrome and SHFM: Report of Two Cases and Mutation Analysis of p63 Gene Abstract Similar Articles Mail to Editor Baboon Syndrome Induced by Oral Antitussive-Decongestant Agent in a Child Abstract Similar Articles Mail to Editor Reye Syndrome and Liver Transplantation Abstract Similar Articles Mail to Editor Pediatric Pulmonology in a Developing Country: Our focus Abstract Similar Articles Mail to Editor Hypothyroidism-Associated Testicular Enlargement: Is It a Form of Precocious Puberty or Not? A Case Report Abstract Similar Articles Mail to Editor Hematogones in Immune Thrombocytopenic Purpura: Diagnostic Implication Abstract Similar Articles Mail to Editor Asperger's Disorder and Williams Syndrome: A Case Report Abstract Similar Articles Mail to Editor The Relationship between Renal P-Glycoprotein Expression and Response to Steroid Therapy in Childhood Nephrotic Syndrome Abstract Similar Articles Mail to Editor Diet and Physical Activity Interventions Do Have Effects on Body Composition and Metabolic Syndrome Parameters in Overweight and Obese Adolescents and Their Mothers Abstract Similar Articles Mail to Editor Early-Onset Basal Cell Carcinoma Abstract Similar Articles Mail to Editor Posterior Reversible Encephalopathy Syndrome due to Pulse Methylprednisolone Therapy in a Child Abstract Similar Articles Mail to Editor Hypocalcemic seizure in an adolescent with Down syndrome: a manifestation of unrecognized celiac disease Abstract Similar Articles Mail to Editor The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation Abstract Similar Articles Mail to Editor Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation Abstract Similar Articles Mail to Editor Scientific Publications in Pediatrics over the Last Ten Years in Turkey and Worldwide Abstract Similar Articles Mail to Editor Evaluation of Late Effects of Postoperative Radiotherapy in Patients with Medulloblastoma Abstract Similar Articles Mail to Editor A Newborn with Trisomy 13 Presenting with Cloacal Exstrophy Abstract Similar Articles Mail to Editor Determination of Helicobacter pylori Antibiotic Resistance Patterns in Pediatric Gastroenterology Patients: The Hacettepe Experience Abstract Similar Articles Mail to Editor Turkish Cases of Early Infantile Epileptic Encephalopathy: Two Novel Mutations in the Cyclin-Dependent Kinase-Like 5 (CDKL5) Gene Abstract Similar Articles Mail to Editor Chanarin–Dorfman Syndrome: A Novel Mutation in a Turkish Girl Abstract Similar Articles Mail to Editor Celiac disease in patients with Williams-Beuren syndrome Abstract Similar Articles Mail to Editor The relation between mean platelet volume and mortality in critical pediatric patients Abstract Similar Articles Mail to Editor Testicular cavernous hemangioma presenting as an ipsilateral lesion in a child with multicystic dysplastic kidney Abstract Similar Articles Mail to Editor Kawasaki disease shock syndrome: a rare and severe complication of Kawasaki disease Abstract Similar Articles Mail to Editor Is anti-Mullerian hormone an indicator of potential polycystic ovary syndrome in prepubertal girls with simple obesity? Abstract Similar Articles Mail to Editor Oxygen therapy via high flow nasal cannula in pediatric intensive care unit Abstract Similar Articles Mail to Editor Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey Abstract Similar Articles Mail to Editor Fatal paraphenylenediamine poisoning due to black henna Abstract Similar Articles Mail to Editor Severe theophylline poisoning treated with continuous venovenous hemodialysis in a child Abstract Similar Articles Mail to Editor Horseshoe kidney with growth retardation: Don’t forget Turner syndrome Abstract Similar Articles Mail to Editor Nasal chondromesenchymal hamartoma, a rare pediatric tumor: Case report Abstract Similar Articles Mail to Editor Different clinical spectrum of leptospirosis Abstract Similar Articles Mail to Editor Parotidectomy outcomes, diagnosis and complications on pediatric patients; Twelve years of experiences in a tertiary care center Abstract Similar Articles Mail to Editor A novel de novo mutation involving the MLL2 gene in a Kabuki syndrome patient presenting with seizures Abstract Similar Articles Mail to Editor A case with atrophic autoimmune thyroiditis-related hypothyroidism causing multisystem involvement in early childhood Abstract Similar Articles Mail to Editor Factors affecting survival in neonatal surgery unit in a tertiary care university hospital during 26 years Abstract Similar Articles Mail to Editor Asthma control test and pediatric asthma quality of life questionnaire association in children with poor asthma control Abstract Similar Articles Mail to Editor A new emerging problem in pediatric emergency units: Synthetic cannabinoids Abstract Similar Articles Mail to Editor Comparison of risk scoring systems in congenital heart surgery Abstract Similar Articles Mail to Editor Primary intrarenal neuroblastoma in a 13-month-old girl presenting as a Wilms' tumor with pulmonary metastasis Abstract Similar Articles Mail to Editor Peutz-Jeghers syndrome: an unusual cause of recurrent intussusception in a 7-year-old boy Abstract Similar Articles Mail to Editor Coexistence of early onset sarcoidosis and partial interferon-γ receptor 1 deficiency Abstract Similar Articles Mail to Editor Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticular leiomyoma: A case report Abstract Similar Articles Mail to Editor Parapharyngeal giant ganglioneuroma with multifocal bone involvement in a pediatric female patient Abstract Similar Articles Mail to Editor Response to cimetidine in a 1-year-old child with PFAPA syndrome Abstract Similar Articles Mail to Editor Normal sweat chloride test does not rule out cystic fibrosis Abstract Similar Articles Mail to Editor Polyposis deserves a perfect physical examination for final diagnosis: Bannayan-Riley-Ruvalcaba syndrome Abstract Similar Articles Mail to Editor Congenital insensitivity to pain: How should anesthesia be managed? Abstract Similar Articles Mail to Editor High frequency oscillatory ventilation versus conventional mechanical ventilation in pediatric acute respiratory distress syndrome: A randomized controlled study Abstract Similar Articles Mail to Editor Comparison of weight estimation methods and evaluation of usability of Broselow Luten tape in Turkish children Abstract Similar Articles Mail to Editor Incidence, risk factors and treatment outcomes of drug extravasation in pediatric patients in China Abstract Similar Articles Mail to Editor Successful treatment of a childhood synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome with subcutaneous methotrexate: A case report Abstract Similar Articles Mail to Editor Congenital heart defects in Williams syndrome Abstract Similar Articles Mail to Editor Cow`s milk protein allergy awareness and practice among Turkish pediatricians: A questionnaire-survey Abstract Similar Articles Mail to Editor The behavior pattern of parents of patients with subacute sclerosing panencephalitis concerning alternative medicine Abstract Similar Articles Mail to Editor Current information about vaccination practice in pediatric rheumatic diseases and recommendations for future applications Abstract Similar Articles Mail to Editor Evaluation of antimicrobial susceptibilities and virulence factors of Staphylococcus aureus strains isolated from community-acquired and health-care associated pediatric infections Abstract Similar Articles Mail to Editor Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations Abstract Similar Articles Mail to Editor Febrile infection-related epilepsy syndrome (FIRES) treated with immunomodulation in an 8-year-old boy and review of the literature Abstract Similar Articles Mail to Editor Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations Abstract Similar Articles Mail to Editor A rare large mutation involving two exons of the SP-B gene in an infant with severe respiratory distress Abstract Similar Articles Mail to Editor Frequency and outcomes of endotracheal intubation in the pediatric emergency department Abstract Similar Articles Mail to Editor B-type natriuretic peptide is a useful biomarker predicting disease severity in children with isolated bronchiolitis in the emergency department Abstract Similar Articles Mail to Editor Hemolytic uremic syndrome with multiple organ involvement secondary to complement factor H p.Arg1215X mutation Abstract Similar Articles Mail to Editor A case with Rubinstein–Taybi syndrome: A novel frameshift mutation in the CREBBP gene Abstract Similar Articles Mail to Editor Primary trimethylaminuria (fish odor syndrome) and hypothyroidism in an adolescent Abstract Similar Articles Mail to Editor Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome Abstract Similar Articles Mail to Editor Cerebral oxygen saturation monitoring in pediatric cardiopulmonary resuscitation patients in the emergency settings: A small descriptive study Abstract Similar Articles Mail to Editor Leptospirosis in a child with acute respiratory distress syndrome Abstract Similar Articles Mail to Editor A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis Abstract Similar Articles Mail to Editor First manifestation of citrullinemia type I as Sandifer syndrome Abstract Similar Articles Mail to Editor Squamous cell carcinoma associated with Xeroderma pigmentosum: an unusual presentation with a tremendously huge mass over the face and paraneoplastic hypercalcemia-hyperleukocytosis Abstract Similar Articles Mail to Editor A genuine pediatric parapharyngeal abscess a year after uneventful adenotonsillectomy Abstract Similar Articles Mail to Editor Twin reversed arterial perfusion syndrome in a monochorionic monoamniotic twin pregnancy Abstract Similar Articles Mail to Editor Clinical and molecular evaluation of 16 patients with Rett syndrome Abstract Similar Articles Mail to Editor C1q nephropathy among children with nephrotic syndrome: Ten-year experience from a pediatric nephrology unit Abstract Similar Articles Mail to Editor Assessment of central venous catheterization and complications in a tertiary pediatric intensive care unit Abstract Similar Articles Mail to Editor Restless leg syndrome in children with celiac disease Abstract Similar Articles Mail to Editor Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not? Abstract Similar Articles Mail to Editor Acute peripheral facial paralysis following varicella infection: An uncommon complication Abstract Similar Articles Mail to Editor Pediatric primary anaplastic ganglioglioma with malignant neuronal component Abstract Similar Articles Mail to Editor Phenytoin induced dystonia Abstract Similar Articles Mail to Editor Association of dysglycemia with mortality in children receiving parenteral nutrition in pediatric intensive care unit Abstract Similar Articles Mail to Editor Evaluation of Restless Legs syndrome and growing pains in children with familial Mediterranean fever Abstract Similar Articles Mail to Editor Acute renal failure due to severe hypercalcemia and nephrocalcinosis treated with two doses of pamidronate in an infant with Williams-Beuren syndrome Abstract Similar Articles Mail to Editor Ogilvie syndrome presenting with septic shock Abstract Similar Articles Mail to Editor Efficacy of rufinamide in childhood refractory epilepsy Abstract Similar Articles Mail to Editor A novel mutation of the MYH7 gene in a patient with hypertrophic cardiomyopathy Abstract Similar Articles Mail to Editor Polyarteritis nodosa in case of familial Mediterranean fever Abstract Similar Articles Mail to Editor Arthropathy-like findings and a carpal tunnel syndrome as the presenting features of Scheie syndrome: Three cases from the same family Abstract Similar Articles Mail to Editor Evaluation of autonomic nervous system functions in frame of heart rate variability in children with inflammatory bowel disease in remission Abstract Similar Articles Mail to Editor Venous thromboembolism in two adolescents with Down syndrome Abstract Similar Articles Mail to Editor Is the BCS1L variant c.232A>G truly responsible for a GRACILE-like condition? Abstract Similar Articles Mail to Editor Outcome of out-of-hospital cardiopulmonary arrest in children: A multicenter cohort study Abstract Similar Articles Mail to Editor Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain Abstract Similar Articles Mail to Editor Pulmonary thromboendarterectomy in pediatric patients: Report of three cases Abstract Similar Articles Mail to Editor Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome Abstract Similar Articles Mail to Editor Sustained hyperferritinemia in a child with macrophage activation syndrome secondary to systemic juvenile idiopathic arthritis - perforinopathy: case based review Abstract Similar Articles Mail to Editor Home accident or physical abuse: Evaluation of younger children presenting with trauma, burn and poisoning in the Pediatric Emergency Department Abstract Similar Articles Mail to Editor Evaluation of pediatric patients with an oncologic emergency: Single center experience Abstract Similar Articles Mail to Editor Does inhaled salbutamol before surfactant therapy have any beneficial effect? Abstract Similar Articles Mail to Editor Complications of cardiac catheterization in children with congenital heart disease Abstract Similar Articles Mail to Editor Association of lactate/albumin ratio level to organ failure and mortality in severe sepsis in a pediatric intensive care unit in Egypt Abstract Similar Articles Mail to Editor Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems Abstract Similar Articles Mail to Editor A patient heterozygous for R92Q mutation with periodic fever and aphthous stomatitis, pharyngitis, and adenitis (PFAPA) syndrome-like phenotype Abstract Similar Articles Mail to Editor Primary cutaneous lymphoma in children: A report of four cases Abstract Similar Articles Mail to Editor Aneurysmal bone cyst in the inferior nasal turbinate in a pediatric patient: A case report Abstract Similar Articles Mail to Editor Management of NSAID-related pyloric obstruction in a child using endoscopic balloon dilatation: A case report Abstract Similar Articles Mail to Editor
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