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Ficicioglu C
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Conducting an investigator-initiated randomized double-blinded intervention trial in acute decompensation of inborn errors of metabolism: Lessons from the N-Carbamylglutamate Consortium
Low bone mineral density is a common finding in patients with homocystinuria
Dihydropteridine reductase deficiency and treatment with tetrahydrobiopterin: a case report
Genotype-phenotype correlations: sudden death in an infant with very-long-chain acyl-CoA dehydrogenase deficiency
Very long-chain acyl-CoA dehydrogenase deficiency in a patient with normal newborn screening by tandem mass spectrometry
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