✦ LIBER ✦

Mitochondrial function in Huntington's disease: Clues for pathogenesis and prospects for treatment

✍ Scribed by A. H. V. Schapira

Publisher: John Wiley and Sons
Year: 1997
Tongue: English
Weight: 228 KB
Volume: 41
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.410410203

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Premotor Parkinson's disease: Clinical f

Premotor Parkinson's disease: Clinical features, detection, and prospects for treatment

✍ Andrew Siderowf; Matthew B. Stern 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 136 KB 👁 2 views

Questions and problems in direct predict

Questions and problems in direct predictive testing for Huntington's disease

✍ Tóth, Tamás; Papp, Csaba; Németi, Margit; Papp, Zoltán 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 3 KB 👁 2 views

Mitochondrial pathology in Parkinson's d

Mitochondrial pathology in Parkinson's disease and implications for therapeutic intervention

✍ Russell H. Swerdlow; W. Davis Parker Jr. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 87 KB 👁 2 views

Although the ultimate origin and role of mitochondrial pathology in Parkinson's disease (PD) remains controversial, accumulating data suggest that mitochondrial dysfunction is genetic and plays an important role in neurodegeneration. PD mitochondria display abnormal electron transport chain activity

Experience in prenatal testing for Hunti

Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987–1997)

✍ Anneke Maat-Kievit; Maria Vegter-van der Vlis; Moniek Zoeteweij; Monique Losekoo 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 169 KB 👁 1 views

We have performed 31 exclusion tests (43 per cent) and 41 direct tests (57 per cent) in 43 couples at risk, in the period 1987 to 1997 in Leiden, The Netherlands. This resulted in termination of 28 pregnancies (39 per cent), with an increased risk. In 28 couples (65 per cent), the woman was at risk.

Preimplantation diagnosis for Huntington

Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos

✍ K. Sermon; V. Goossens; S. Seneca; W. Lissens; A. de Vos; M. Vandervorst; A. van 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 188 KB 👁 1 views

Huntington's disease (HD) is an autosomal dominant disease characterized by motor disturbance, cognitive loss and psychiatric manifestations, starting between the fourth and the fifth decade, followed by death within 10-20 years of onset of the disease. The disease-causing mutation is an expansion o

Efficacy and safety of alendronate for t

Efficacy and safety of alendronate for the treatment of osteoporosis in diffuse connective tissue diseases in children: A prospective multicenter study

✍ Maria Luisa Bianchi; Rolando Cimaz; Maria Bardare; Francesco Zulian; Loredana Le 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 93 KB 👁 1 views

Values are the number of patients or the mean Ϯ SD. † Behçet's syndrome (2 patients), Wegener's granulomatosis (1 patient), and undefined connective tissue disease (2 patients). ‡ Prednisone equivalents.