Charcot-Marie-Tooth Disorders: Pathophysiology, Molecular Genetics and Therapy (Neurology & Neurobiology Series)

Partial table of contents: CLINICAL STUDIES AND PATHOLOGICAL ALTERATIONS. Hereditary Motor and Sensory Neuropathy Types I and II (A. Harding). Charcot-Marie-Tooth ''Plus22 and Heterogeneity: Clinical and Electrophysiological Studies (R. Lovelace). Familial Spastic Paraplegia with Peroneal Atrophy (9 Cases) (C. Serratrice, et al.). Giant Axons in an Autosomal-Dominant Hereditary Neuropathy--A Variant of Peroneal Muscular Atrophy? (H. Goebel, et al.). CLINICAL NEUROPHYSIOLOGY AND HETEROGENEITY. Electrophysiological Study of 231 Patients with Peroneal Muscular Atrophy Types I and II: Heretogeneity According to Duffy Locus Linkage (P. Bouche, et al.). Serial Nerve Conduction Studies in Charcot-Marie-Tooth Disease ( HMSN-I) (L. Gutmann, et al.). Hereditary Polyneuropathy With ''NO-NO22 Head Tremor, Ataxia and Cerebellar Atrophy (A. Jusbreve;icacute; & O. Sinanovicacute;). AXONAL AND SCHWANN CELL METABOLISM AND IMMUNE FACTORS. Schwann Cells and the Immune System (K. Jessen, et al.). The Unexpected Expression of the Major CNS Myelin Protein, Proteolipid Protein, in Schwann Cells In Vivo and In Vitro (K. Ono, et al.). Immune Mechanisms in Hereditary Neuropathies (S. Kahn & N. Latov). LINKAGE STUDIES ON HEREDITARY MOTOR AND SENSORY NEUROPATHIES. Linkage Studies on Hypertrophic Motor and Sensory Neuropathy Type I (L. Griffiths, et al.). Chromosomal Location of the CMT I Gene by CBG-Banding (L. Williams, et al.). Charcot-Marie-Tooth Disease (HMSN-I) Concurrence with Von Willebrand Disease and Short Stature (J. Lupski, et al.). METABOLIC STUDIES, EXPERIMENTAL DRUG TRIALS, SURGERY, AND PHYSIOTHERAPY. Metabolic Screening Studies on Charcot-Marie-Tooth Disease (H. Shapiro & G. Kahn). Review: Effects of Dietary Linoleic (Omega-6) Fatty Acid and Vitamin E Supplementation on Type I CMT Serum Fatty Acids and Physical Performance (L. Williams, et al.). Index.Lovelace, Robert E. is the author of 'Charcot-Marie-Tooth Disorders: Pathophysiology, Molecular Genetics and Therapy (Neurology & Neurobiology Series)' with ISBN 9780471562344 and ISBN 0471562343.