The Turkish Journal of Pediatrics
Smilar Issues: 21 Record Found
Hypercalciuria and nephrocalcinosis in cystic fibrosis patients Abstract Similar Articles Mail to Editor Using computer based data acquisition and analysis system for nasal potential difference measurement in cystic fibrosis Abstract Similar Articles Mail to Editor Modified oral rehydration therapy in a case with cystic fibrosis Abstract Similar Articles Mail to Editor Long-Term Clarithromycin in Cystic Fibrosis: Effects on Inflammatory Markers in BAL and Clinical Status Abstract Similar Articles Mail to Editor Cystic fibrosis with acute myelogenous leukemia Abstract Similar Articles Mail to Editor Screening for liver disease in cystic fibrosis: analysis of clinical and genetic risk factors for its development Abstract Similar Articles Mail to Editor Cystic fibrosis in a boy with meconium ileus and mild clinical phenotype associated with 2183AA-G/D1152H genotype Abstract Similar Articles Mail to Editor The Clinical and Laboratory Manifestations of Iranian Patients with Cystic Fibrosis Abstract Similar Articles Mail to Editor Anti-neutrophil cytoplasmic antibodies (ANCA) in serum and bronchoalveolar lavage fluids of cystic fibrosis patients and patients with idiopathic bronchiectasis Abstract Similar Articles Mail to Editor Sweat Conductivity Test: Can It Replace Chloride Titration for Cystic Fibrosis Diagnosis? Abstract Similar Articles Mail to Editor The Role of Serum Pseudomonas aeruginosa Antibodies in the Diagnosis and Follow-Up of Cystic Fibrosis Abstract Similar Articles Mail to Editor Effect of Supplementary Zinc on Body Mass Index, Pulmonary Function and Hospitalization in Children with Cystic Fibrosis Abstract Similar Articles Mail to Editor The effect of probiotics on fecal calprotectin in patients with cystic fibrosis Abstract Similar Articles Mail to Editor Long term azithromycin therapy in patients with cystic fibrosis Abstract Similar Articles Mail to Editor Diagnosis of cystic fibrosis with chloride meter (Sherwood M926S chloride analyzer®) and sweat test analysis system (CFΔ collection system®) compared to the Gibson Cooke method Abstract Similar Articles Mail to Editor Changing epidemiology of non-cystic fibrosis bronchiectasis Abstract Similar Articles Mail to Editor Normal sweat chloride test does not rule out cystic fibrosis Abstract Similar Articles Mail to Editor Psychiatric morbidity and quality of life in children and adolescents with cystic fibrosis Abstract Similar Articles Mail to Editor Meconium periorchitis: An incidentally diagnosed rare entity during inguinal herniorraphy Abstract Similar Articles Mail to Editor Nasal nitric oxide levels in primary ciliary dyskinesia, cystic fibrosis and healthy children Abstract Similar Articles Mail to Editor A rare clinical association: Barth syndrome and cystic fibrosis Abstract Similar Articles Mail to Editor
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