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Morvan Syndrome: Clinical and Serological Observations in 29 Cases
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Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992
Autonomic Epilepsy:Clonidine Blockade of Paroxysmal Catecholamine Release & Flushing
Ann Int Med 88:189, Metz,S.A.,et al, 1978
Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
Ann Neurol 3:464, Waybright,E.A.,et al, 1978
The Neurologist's Experience with Pheochromocytoma
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