The Turkish Journal of Pediatrics
Smilar Issues: 37 Record Found
Tubular functions in familial Mediterranean fever Abstract Similar Articles Mail to Editor Comparison of thicknesses of the myocardial fibers of anencephalic and normal human fetuses Abstract Similar Articles Mail to Editor The oral health status of children undergoing hemodialysis treatment Abstract Similar Articles Mail to Editor Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients Abstract Similar Articles Mail to Editor Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I) Abstract Similar Articles Mail to Editor Malformations of cortical development and epilepsy: evaluation of 101 cases (Part II) Abstract Similar Articles Mail to Editor A rare cause of neonatal seizure: incontinentia pigmenti Abstract Similar Articles Mail to Editor Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract 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 Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes Abstract Similar Articles Mail to Editor Type 1 diabetes mellitus associated with autoimmune thyroid disease, celiac disease and familial Mediterranean fever: case report 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 Penile Size in Term Newborn Infants Abstract Similar Articles Mail to Editor A Rare Case of 2q37 Microdeletion with Albright Hereditary Osteodystrophy-Like Phenotype Abstract Similar Articles Mail to Editor One-Year Follow-up of Penis and Testis Sizes of Healthy Turkish Male Newborns 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 Soft Tissue Infection Caused by Burkholderia cepacia in a Child with Polyarteritis Nodosa 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 Diagnostic Dilemma in Autoinflammatory Disease in Two Patients: Does the Name Matter? Abstract Similar Articles Mail to Editor Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report Abstract Similar Articles Mail to Editor An antenatal appearance of megacystis-microcolon-intestinal hypoperistalsis syndrome Abstract Similar Articles Mail to Editor Relation between microalbuminuria and gene mutations in familial Mediterranean fever Abstract Similar Articles Mail to Editor Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue Abstract Similar Articles Mail to Editor An unusual presentation of cardiomyopathy in a patient with microcephaly-cardiomyopathy syndrome Abstract Similar Articles Mail to Editor Neuroendocrine Immune System in Familial Mediterranean Fever Abstract Similar Articles Mail to Editor Three Cases of a Rare Disease, Congenital Chloride Diarrhea, Summons Up the Variation in the Clinical Course and Significance of Early Diagnosis and Adequate Treatment in the Prevention of Intellectual Disability Abstract Similar Articles Mail to Editor Chronic kidney disease in an adolescent with hyperuricemia: familial juvenile hyperuricemic nephropathy Abstract Similar Articles Mail to Editor Familial Mediterranean fever associated with optic neuritis, successfully treated with anti-interleukin 1 agents Abstract Similar Articles Mail to Editor An unexpected diagnostic course of systemic lupus erythematosus Abstract Similar Articles Mail to Editor Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever 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 Child with RET proto-oncogene codon 634 mutation Abstract Similar Articles Mail to Editor Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency Abstract Similar Articles Mail to Editor Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region 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 GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria Abstract Similar Articles Mail to Editor Polyarteritis nodosa in case of familial Mediterranean fever Abstract Similar Articles Mail to Editor
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