Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992
The Neurologist's Experience with Pheochromocytoma
JAMA 197:100, Thomas,J.E.,et al, 1966
Glucose Hypermetabolism in the Basal Ganglia
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The Writing on the Wall
Lancet 372:344, Wilder-Smith,E.P. &Ng,E.S., 2008
Unilateral Localized Hyperhidrosis Associated With Frontal Lobe Meningioma
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Hemiplegia Vegetativa Alterna (Ipsilateral Horner's Synd & Contralat Hemihyperhidrosis) Post Cerebral Art Occl
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Acromegaly:Clinical and Biochemical Features in 500 Patients
Medicine 73:233-240, Ezzat,S.,et al, 1994
Acute Mercury Poisoning (Acrodynia) Mimicking Pheochromocytoma in an Adolescent
J Pediatr 122:252-253, Henningsson,C.,et al, 1993
Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993
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
Acromegaly
NEJM 322:966-977, Melmed,S., 1990
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
Juvenile Type of Distal & Segmental Muscular Atrophy of Upper Extremities
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Hyperhydrosis in Paraplegia
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