Glycogen storage disease type I a: Frequency and clinical course in Turkish children

Author:

Saltik Inci Nur,Özen Hasan,Ciliv Gönenç,Koçak Nurten,Yüce Aysel,Gürakan Figen,Dinler Gönül

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference31 articles.

1. Roy CC, Silverman A, Alagille D. Inborn errors of metabolism. In:Pediatric Clinical Gastroenterology, 4th edn, USA; Mosby-Year Book, Inc, 1995; 816–876.

2. Nyhan WL, Özand PT. Glycogenosis type Ia/Von Gierke disease/Glucose-6-phosphatase deficiency. In:Atlas of Metabolic Disease, 1st edn, London: Chapman & Hall Medical, 1998; 330–340.

3. Hug C, Chuck G, Tsoras M. Increased serum biotinidase activity in glycogen storage disease type Ia.Pediatr Res 1994; 35: 203A.

4. Lee PJ, Leonard JV. The hepatic glycogen storage disease problems beyond the childhood.J Inher Metab Dis 1995; 18: 462–472.

5. Lei K, Shely LL, Pan C, Sidbury JB, Chou JY. Mutations in the glucose-6 phosphatase gene that cause glycogen storage disease type Ia.Science 1993; 262: 580–583.

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