✦ LIBER ✦

Therapy of Fabry disease

✍ Scribed by Kleinert, Julia; Hauser, Anna-Christine; Lorenz, Matthias; Fodinger, Manuela; Sunder-Plassmann, Gere

Book ID: 109066888
Publisher: Nature Publishing Group
Year: 2004
Tongue: English
Weight: 45 KB
Volume: 66
Category: Article
ISSN: 0085-2538
DOI: 10.1111/j.1523-1755.2004.884_1.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Fabry disease: enzyme replacement therap

Fabry disease: enzyme replacement therapy

✍ MR Bongiorno; G Pistone; M Aricò 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 164 KB

## ABSTRACT Fabry disease is a multisystem disorder associated with wide variability in clinical expression. Fabry disease is an X‐linked lysosomal storage disorder caused by a deficiency of α‐galactosidase A. The enzyme defect leads to the systemic accumulation of glycosphingolipids with α‐galacto

Clinical benefit of enzyme replacement t

Clinical benefit of enzyme replacement therapy in Fabry disease

✍ Breunig, F; Weidemann, F; Strotmann, J; Knoll, A; Wanner, C 📂 Article 📅 2006 🏛 Nature Publishing Group 🌐 English ⚖ 113 KB

Fabry disease: Kidney involvement and en

Fabry disease: Kidney involvement and enzyme replacement therapy

✍ Siamopoulos, Kostas C. 📂 Article 📅 2004 🏛 Nature Publishing Group 🌐 English ⚖ 139 KB

Enzyme replacement therapy in an adolesc

Enzyme replacement therapy in an adolescent with Fabry disease

✍ Sabine Illsinger; Thomas Luecke; Hendrik Langen; Anibh M. Das 📂 Article 📅 2003 🏛 Springer 🌐 English ⚖ 154 KB

Neurology of Fabry disease

✍ M. Low; K. Nicholls; N. Tubridy; P. Hand; D. Velakoulis; L. Kiers; P. Mitchell; 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 344 KB

Fabry's disease

✍ J. Crouzet; L. Beraneck; Y. Le Charpentier; R. Abelanet 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 119 KB