Glycogen storage disease type I a: Frequency and clinical course in Turkish children-Reference-Cited by-同舟云学术

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

Published:2000-07 Issue:7 Volume:67 Page:497-501
ISSN:0019-5456
Container-title:The Indian Journal of Pediatrics
language:en
Short-container-title:Indian J Pediatr

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

Link

http://link.springer.com/content/pdf/10.1007/BF02760476.pdf

Reference31 articles.

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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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