The Turkish Journal of Pediatrics
Smilar Issues: 8 Record Found
Neonatal screening
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Detection of other inborn errors of metabolism in hyperphenylalaninemic babies picked up on narrow-spectrum screening programs
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Sapropterin Dihydrochloride Treatment in Turkish Hyperphenylalaninemic Patients under Age Four
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Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments
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Cognitive and behavioral impairment in mild hyperphenylalaninemia
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Thirty years of the newborn screening program in Central Serbia: the missed cases of congenital hypothyroidism
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Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience
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Clinical and molecular findings in 6 Turkish cases with Krabbe disease
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