✦ LIBER ✦

Glycogen storage disease type III with diagnosis complicated by gluten-sensitive enteropathy

✍ Scribed by R. Artan; O.P. van Diggelen; J.G.M. Huijmans

Book ID: 110222835
Publisher: Springer
Year: 1998
Tongue: English
Weight: 60 KB
Volume: 21
Category: Article
ISSN: 0141-8955
DOI: 10.1023/a:1005331414257

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Severe hypoglycaemia in a patient with g

Severe hypoglycaemia in a patient with glycogen storage disease type III induced by infectious mononucleosis

✍ T. Kimura; H. Ikeda; M. Kato; A. Ito; M. Okubo; K. Hayasaka 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 34 KB

PRENATAL DIAGNOSIS IN A CHINESE FAMILY W

PRENATAL DIAGNOSIS IN A CHINESE FAMILY WITH TYPE Ia GLYCOGEN STORAGE DISEASE BY PCR-BASED GENETIC ANALYSIS

✍ WEN-JANE LEE; CHING-HWA YANG; ESTHER SHIH-CHU HO; AI SHIH; LIH-YUAN LIN; WEN-HAN 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 623 KB

Type Ia glycogen storage disease (GSD), an autosomal recessive metabolic disorder, is caused by a deficiency in glucose-6-phosphatase (G6Pase). We had previously identified the nature of the causative mutations in a Chinese family whose first two children were affected with type Ia GSD. Two differen

Verification of diagnosis in a 17-year-o

Verification of diagnosis in a 17-year-old boy with clinical glycogen storage disease type Ia by mutation screening

✍ D. Matern; H. Niederhoff; M. Brandis; J. Y. Chou 📂 Article 📅 1996 🏛 Springer 🌐 English ⚖ 388 KB