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Download Charcot-Marie-Tooth disorders: Pathophysiology, molecular genetics, and therapy (Neurology and neurobiology) fb2, epub

Download Charcot-Marie-Tooth disorders: Pathophysiology, molecular genetics, and therapy (Neurology and neurobiology) fb2, epub

ISBN: 0845127578
Language: English
Publisher: Liss (1989)
Category: Basic Sciences
Subcategory: Medicine
Rating: 4.6
Votes: 890
Size Fb2: 1858 kb
Size ePub: 1557 kb
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SYMPTOMS OF CHARCOT MARIE TOOTH DISEASE - Продолжительность: 2:47 .

Неумывакин Шум в голове Часть 1 - Продолжительность: 9:30 Alexander Zakurdaev Recommended for you.

This volume provides a contemporary evaluation of a diverse.

Unlike other neurology textbooks that either focus on neuroanatomy or clinical neurology, Clinical Neurology and Neuroanatomy integrates the two in manner which simulates the way neurologists learn, teach, and think. Clinical Neurology and Neuroanatomy is divided into two main sections.

The book explains the pathophysiology, molecular mechanisms, clinical manifestations, and .

New York: Wiley-Liss, 1990. Lupski, J. R., et al. (1992). Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1 A. Nature Genetics 1, 29-33. Murakami, T. (1996). Charcot-Marie-Tooth Disease and Related Inherited Neuropathies. Medicine 75, 233-250. Roa, B. B., et. al. Duplication of the PMP 22 gene in 17 p partial trisomy patients with Charcot-Marie-Tooth type-1 A neuropathy.

ISBN 13: 9780845127575.

CMT was previously classified as a subtype of muscular dystrophy.

The disease described by Charcot and Marie involves a slowly progressive distal muscular atrophy with initial . 1992, Molecular genetics and neuropathology of Charcot-Marie-Tooth disease type 1A, Brain Pathology 2:337–349.

The disease described by Charcot and Marie involves a slowly progressive distal muscular atrophy with initial involvement of the feet and legs, followed by variable progressive weakness of the hands. PubMedGoogle Scholar. 1992, Short, interspersed repetitive DNA sequences in prokaryotic genomes.

CMT is characterized by inherited neuropathies without known metabolic derangements. Its genetic spectrum spans more than 80 genes. Gene discovery has been revolutionized by new high-throughput molecular technologies. CMT disease is divided into several types, as follows.

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