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Brain, Vol. 121, Iss. 2, 1998-02 ,pp. : 303-316

Oxford University Press

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Retinal vasculopathy in autosomal dominant neurofibromatosis type 1

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Informa Healthcare

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A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family

By Delague Valérie   Bareil Corinne   Bouvagnet Patrice   Salem Nabiha   Chouery Eliane   Loiselet Jacques   Mégarbané André   Claustres Mireille  

Neurogenetics, Vol. 4, Iss. 1, 2002-03 ,pp. : 23-27

Springer Publishing Company

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Late onset autosomal dominant Charcot–Marie–Tooth 2 neuropathy in a Costa Rican family

By Berghoff Corinna   Berghoff Martin   Leal Alejandro   Morera Bernal   Contreras Carlos   Barrantes Ramiro   Rautenstrauss Bernd   Del Valle Gerardo   Heuss Dieter  

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Familial temporal lobe epilepsy - Autosomal dominant inheritance in a large pedigree from Southern Italy

By Gambardella A.   Messina D.   Le Piane E.   Oliveri R.L.   Annesi G.   Zappia M.   Andermann E.   Quattrone A.   Aguglia U.  

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