✦ LIBER ✦

M wave changes with temperature in amyotrophic lateral sclerosis and disorders of neuromuscular transmission

✍ Scribed by Dr. Eric H. Denys

Publisher: John Wiley and Sons
Year: 1990
Tongue: English
Weight: 444 KB
Volume: 13
Category: Article
ISSN: 0148-639X
DOI: 10.1002/mus.880130709

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Linear estimates of disease progression

Linear estimates of disease progression predict survival in patients with amyotrophic lateral sclerosis

✍ Carmel Armon; Michael C. Graves; Dharmaseli Moses; Delano K. Forté; Linda Sepulv 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 165 KB 👁 2 views

We have shown that linear estimates of rates of disease progression (LEP), derived from isometric myometry [grip or foot dorsiflexion (FD) strength] and forced vital capacity (FVC%), are clinically and statistically significant predictors of survival of patients with amyotrophic lateral sclerosis (A

Voxel-based morphometry study of brain v

Voxel-based morphometry study of brain volumetry and diffusivity in amyotrophic lateral sclerosis patients with mild disability

✍ F. Agosta; E. Pagani; M.A. Rocca; D. Caputo; M. Perini; F. Salvi; A. Prelle; M. 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 195 KB

## Abstract Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by the progressive and simultaneous degeneration of upper and lower motor neurons. The pathological process associated to ALS, albeit more pronounced in the motor/premotor cortices and along the corticospin

Molecular analysis of the superoxide dis

Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis

✍ A. García-Redondo; F. Bustos; B. Juan Y Seva; P. Del Hoyo; S. Jiménez; Y. Campos 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 277 KB

Novel 4-bp insertion in exon 5 of the Cu

Novel 4-bp insertion in exon 5 of the CuZn-superoxide dismutase (SOD1) gene associated with familial amyotrophic lateral sclerosis

✍ Claus Hansen; Ole Gredal; Lene Werdelin; Peter M. Andersen; Stefan L. Marklund; 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB

Mutations in the gene for low density lipoprotein receptor (LDL-R) lead to a disorder called familial hypercholesterolemia (FH). Affected individuals are characterized by increased levels of cholesterol in plasma, tendinous xanthomas, arcus lipoides corneae, and premature coronary heart disease. Up

Decreased cytochrome c oxidase activity

Decreased cytochrome c oxidase activity but unchanged superoxide dismutase and glutathione peroxidase activities in the spinal cords of patients with amyotrophic lateral sclerosis

✍ K. Fujita; M. Yamauchi; K. Shibayama; M. Ando; M. Honda; Y. Nagata 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 514 KB

The cause of selective degeneration of motor neurons in the ventral horn of the spinal cord associated with amyotrophic lateral sclerosis (ALS) has still not been elucidated. Recently, so-called oxidative stress has been suggested to be a significant factor in the pathogenesis of this disease. We me

Altered oxidative stress profile in the

Altered oxidative stress profile in the cortex of mice fed an enriched branched-chain amino acids diet: Possible link with amyotrophic lateral sclerosis?

✍ P. Piscopo; A. Crestini; A. Adduci; A. Ferrante; M. Massari; P. Popoli; N. Vanac 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 356 KB

## Abstract Branched‐chain amino acids (BCAAs), valine, isoleucine, and leucine, are widely used among athletes as dietary integrators. Although the occurrence of untoward effects of BCCA supplementation, with particular regard to neurological disturbances, cannot be excluded, no specific studies h