✦ LIBER ✦

Health status of boys with Duchenne muscular dystrophy: A parent's perspective

✍ Scribed by Paula Bray; Anita C Bundy; Monique M Ryan; Kathryn N North; Joshua Burns

Book ID: 108956106
Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 297 KB
Volume: 47
Category: Article
ISSN: 1034-4810
DOI: 10.1111/j.1440-1754.2011.02022.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Frequency of new mutants among boys with

Frequency of new mutants among boys with Duchenne muscular dystrophy

✍ Bucher, K. ;Ionasescu, V. ;Hanson, J. ;Optiz, John M. 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 495 KB

Changes in center of gravity in boys wit

Changes in center of gravity in boys with duchenne muscular dystrophy

✍ Ms. Ruth Barrett; Mrs. Sylvia A. Hyde; Dr. Oona M. Scott; Dr. Victor Dubowitz 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 549 KB

Assessment of locomotor function in youn

Assessment of locomotor function in young boys with duchenne muscular dystrophy

✍ Dr.; MRCP Robert A. Smith; Dr.; Phd; FSS Robert G. Newcombe; Dr.; DCH; MD; FRCP 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 615 KB

Compositional analysis of muscle in boys

Compositional analysis of muscle in boys with Duchenne muscular dystrophy using MR imaging

✍ Franklin A. Marden; Anne M. Connolly; Marilyn J. Siegel; David A. Rubin 📂 Article 📅 2004 🏛 Springer 🌐 English ⚖ 402 KB

Magnetic resonance imaging of children w

Magnetic resonance imaging of children with Duchenne muscular dystrophy

✍ A. Schreiber; W. L. Smith; V. Ionasescu; H. Zellweger; E. A. Franken; V. Dunn; J 📂 Article 📅 1987 🏛 Springer-Verlag 🌐 English ⚖ 325 KB

A manifesting carrier of Duchenne muscul

A manifesting carrier of Duchenne muscular dystrophy with severe myocardial symptoms

✍ K. Kamakura; M. Kawai; K. Arahata; H. Koizumi; K. Watanabe; H. Sugita 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 593 KB

A 42-year-old so-called manifesting carrier of Duchenne muscular dystrophy (DMD), whose first complaints were severe myocardial symptoms, is described. Immunohistochemical study using anti-dystrophin anti-serum and analysis of cloned segments of X chromosome DNA were performed. Her two sons and one