The Turkish Journal of Pediatrics
Smilar Issues: 61 Record Found
Tubular functions in familial Mediterranean fever
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Comparison of thicknesses of the myocardial fibers of anencephalic and normal human fetuses
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The oral health status of children undergoing hemodialysis treatment
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Analysis of the modifying effects of SAA1, SAA2 and TNF-alpha gene polymorphisms on development of amyloidosis in FMF patients
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Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I)
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Malformations of cortical development and epilepsy: evaluation of 101 cases (Part II)
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A rare cause of neonatal seizure: incontinentia pigmenti
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Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract
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Familial Mediterranean fever in northwest of Iran (Ardabil): the first global report from Iran
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Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes
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Type 1 diabetes mellitus associated with autoimmune thyroid disease, celiac disease and familial Mediterranean fever: case report
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3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures
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Penile Size in Term Newborn Infants
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A Rare Case of 2q37 Microdeletion with Albright Hereditary Osteodystrophy-Like Phenotype
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One-Year Follow-up of Penis and Testis Sizes of Healthy Turkish Male Newborns
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Prenatally Diagnosed Case of 22q11.2 Deletion Syndrome Associated with Pulmonary Artery Aneurysm
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Soft Tissue Infection Caused by Burkholderia cepacia in a Child with Polyarteritis Nodosa
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Different Presentations in Patients with Tumor Necrosis Factor Receptor-Associated Periodic Syndrome Mutations: Report of Two Cases
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Diagnostic Dilemma in Autoinflammatory Disease in Two Patients: Does the Name Matter?
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Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report
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An antenatal appearance of megacystis-microcolon-intestinal hypoperistalsis syndrome
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Relation between microalbuminuria and gene mutations in familial Mediterranean fever
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Prenatally diagnosed lethal type Larsen-like syndrome associated with bifid tongue
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An unusual presentation of cardiomyopathy in a patient with microcephaly-cardiomyopathy syndrome
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Neuroendocrine Immune System in Familial Mediterranean Fever
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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
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Chronic kidney disease in an adolescent with hyperuricemia: familial juvenile hyperuricemic nephropathy
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Familial Mediterranean fever associated with optic neuritis, successfully treated with anti-interleukin 1 agents
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An unexpected diagnostic course of systemic lupus erythematosus
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Serum vitamin D levels during activation and remission periods of patients with juvenile idiopathic arthritis and familial Mediterranean fever
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Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations
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Child with RET proto-oncogene codon 634 mutation
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Microcephaly and developmental delay caused by short-chain acyl-CoA dehydrogenase deficiency
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Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region
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Evaluation of Restless Legs syndrome and growing pains in
children with familial Mediterranean fever
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GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria
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Polyarteritis nodosa in case of familial Mediterranean fever
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Thrombotic thrombocytopenic purpura as a rare cause of anemia with thrombocytopenia in childhood: report of 2 cases
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Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent
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The lung microbiome in neonates
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A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review
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A rare cause of epileptic encephalopathy: a beta-propeller protein associated neurodegeneration case with a new mutation and literature review
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Canakinumab in colchicine resistant familial Mediterranean fever and other pediatric rheumatic diseases
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Sacroiliitis associated with familial Mediterranean fever in childhood: a case series and review of literature
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Evaluation of micronutrient levels in children and adolescents with obesity and their correlation with the components of metabolic syndrome
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A rare intrauterine onset growth retardation syndrome caused by mosaic 19p13.3 microduplication: evaluation of GH/IGF- 1 axis and GH therapy response
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Altered gut microbiota is associated with feeding intolerance in preterm infants
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Oral health status in children with familial Mediterranean fever
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Expression of MicroRNA 146a, 155, 181 and 223 in febrile seizure
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Parental knowledge about familial Mediterranean fever: a cross-sectional study
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Identification of candidate genes in a family with cancer overload by whole-exome sequencing
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A case of familial recurrent 17q12 microdeletion syndrome presenting with severe diabetic ketoacidosis
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Evaluation of ciliary functions and ciliary beat frequency via cell culture method in patients with primary ciliary dyskinesia
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Autosomal chromosome microdeletions in three adolescent girls with premature ovarian insufficiency: a case report
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Comparison of miRNA expression in patients with seasonal and perennial allergic rhinitis and non-atopic asthma
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3q29 microdeletion syndrome associated with developmental delay and pulmonary stenosis: a case report
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Evaluation of hair structural abnormalities in children with different neurological diseases
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Catastrophic antiphospholipid syndrome accompanied by complement regulatory gene mutation
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Efficacy of antimicrobials or placebo compared to amoxicillin-clavulanate in children with acute otitis media: a systematic review
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Assessing fatigue and related factors in adolescents with familial Mediterranean fever (FMF): psychometric properties of the PedsQL Multidimensional Fatigue Scale
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Fatal thrombotic microangiopathy in an infant with COVID-19: a case report
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