Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes-Reference-Cited by-同舟云学术

Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes

Published:2005-11-22 Issue:2 Volume:36 Page:108-114
ISSN:0301-0449
Container-title:Pediatric Radiology
language:en
Short-container-title:Pediatr Radiol

Author:

Hertz-Pannier Lucie,Déchaux Michele,Sinico Martine,Emond Sophie,Cormier-Daire Valerie,Saudubray Jean-Marie,Brunelle Francis,Niaudet Patrick,Seta Nathalie,de Lonlay Pascale

Publisher

Springer Science and Business Media LLC

Subject

Radiology, Nuclear Medicine and imaging,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00247-005-0001-5.pdf

Reference36 articles.

1. Jaeken J, Carchon H, Stibler H (1993) The carbohydrate-deficient glycoprotein syndromes: pre-Golgi and Golgi disorders? Glycobiology 3:423–428

2. Jaeken J (2003) Komrower lecture. Congenital disorders of glycosylation (CDG): it’s all in it! J Inherit Metab Dis 26:99–118

3. Hutchesson AC, Gray RG, Spencer DA et al (1995) Carbohydrate deficient glycoprotein syndrome; multiple abnormalities and diagnostic delay. Arch Dis Child 72:445–446

4. Jaeken J, Stibler H, Hagberg B (1991) The carbohydrate-deficient glycoprotein syndrome. A new inherited multisystemic disease with severe nervous system involvement. Acta Paediatr Scand Suppl 375:1–71

5. Stibler H, Blennow G, Kristiansson B et al (1994) Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease. J Neurol Neurosurg Psychiatry 57:552–556

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