Electrophysiology of hereditary motor & sensory neuropathy and hereditary spinocerebellar ataxia

By Kiteva-Trencevska G.   Vlaski-Jekic S.   Naumovski R.  

Electroencephalography and Clinical Neurophysiology, Vol. 99, Iss. 4, 1996-10 ,pp. : 317-317

Elsevier

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Hereditary motor and sensory neuropathy - Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings

By Kalaydjieva L   Nikolova A   Turnev I   Petrova J   Hristova A   Ishpekova B   Petkova I   Shmarov A   Stancheva S   Middleton L   Merlini L   Trogu A   Muddle JR   King RHM   Thomas PK  

Brain, Vol. 121, Iss. 3, 1998-03 ,pp. : 399-408

Oxford University Press

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Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology

By Vucic S.   Tian D.   Chong P. Siao Tick   Cudkowicz M. E.   Hedley-Whyte E. T.   Cros D.  

Brain, Vol. 129, Iss. 12, 2006-12 ,pp. : 3384-3390

Oxford University Press

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Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population

By Tüysüz Beyhan  

Neurogenetics, Vol. 9, Iss. 2, 2008-05 ,pp. : 119-125

Springer Publishing Company

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Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I)

By Houlden Henry   King Rosalind   Blake Julian   Groves Mike   Love Seth   Woodward Cathy   Hammans Simon   Nicoll James   Lennox Graham   O'Donovan Dominic G.   Gabriel Carolyn   Thomas P. K.   Reilly Mary M.  

Brain, Vol. 129, Iss. 2, 2006-02 ,pp. : 411-425

Oxford University Press

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