The Turkish Journal of Pediatrics
Smilar Issues: 8 Record Found
Ophthalmologic abnormalities in children from a Turkish school for the deaf
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Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness
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Heart Rate Variability in Children with Congenital Sensorineural Deafness
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Jervell and Lange-Nielsen Syndrome with Homozygous Missense Mutation of the KCNQ1 Gene
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Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation
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Ataxia with vitamin E deficiency associated with deafness
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Arrhythmia in thiamine responsive megaloblastic anemia syndrome
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Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis
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