Reviews And Selected Updates

Bird TD, Kraft GH, Lipe HP, et al: Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth Type 1B: A 20-year study. Ann Neurol 1997;41:463-469.

Chance PF, Fischbeck KH: Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Hum Molec Genet 1994;3:1503- 1507.

Coelho T: Familial amyloid polyneuropathy: New developments in genetics and treatment. Curr Opin Neurol 1996;9:355-359.

England JD, Garcia CA: Electrophysiological studies in the different genotypes of Charcot-Marie-Tooth disease. Curr Opin Neurol 1996;9:338-342.

Eymard B, Romero NB, Leturcq F, et al: Primary adhalinopathy (alpha-sarcoglycanopathy): Clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy. Neurology 1997;48:1227-1234.

Fink JK, Heiman-Patterson T for the Hereditary Spastic Paraplegia Working Group. Hereditary spastic paraplegia: Advances in genetic research. Neurology 1996;46:1507-1514.

Gutmann L, Mitsumoto MD: Advances in amyotrophic lateral sclerosis. Neurology 1996;47:S17-S1235.

Kakulas BA: The differential diagnosis of the human dystrophinopathies and related disorders. Curr Opin Neurol 1996;9:380-388. Siddique T: Motor neuron disease. Clin Neurosci 1995/1996;3:6.

Siddique T, Nijhawan D, Hentati A: Molecular genetic basis of familial ALS. Neurology 1996;47:S27-S34.

Straub V, Campbell KP. Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol 1997;10:168-175.


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