Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mary B. Hans"'
Autor:
Arnulf H. Koeppen, Mary B. Hans
Publikováno v:
The Journal of Nervous and Mental Disease. 168:209-214
Huntington's chorea imposes a direct imprint on the life of the spouse of the affected patient. Interviews with 15 wives of patients with Huntington's chorea revealed that none of them knew prior to marriage of the presence of a heritable disease wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38cae1db38c4fb72ffbbce4ca24117a3
https://doi.org/10.1097/00005053-198004000-00003
https://doi.org/10.1097/00005053-198004000-00003
Publikováno v:
Archives of neurology. 34(10)
• A systematic search for cases of adult-onset hereditary ataxia was conducted on location in Scotland. The investigation resulted in the discovery of eight pedigrees with 42 patients of whom 16 were alive in 1975. Nine patients were examined by th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::953663cc4ad3e49f1887dfa3ee5b8d5d
https://pubmed.ncbi.nlm.nih.gov/907533
https://pubmed.ncbi.nlm.nih.gov/907533
Publikováno v:
Musclenerve. 8(9)
Amyloid fibrils were isolated from the myocardium of two patients with familial amyloid polyneuropathy. The solubilized amyloid fibril whole protein shared immunologic determinants with normal human serum prealbumin (transthyretin), but revealed subt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21214389d6a80eeb34e929fe564e8115
https://pubmed.ncbi.nlm.nih.gov/4079954
https://pubmed.ncbi.nlm.nih.gov/4079954
Autor:
Thomas H. Gilmore, Mary B. Hans
Publikováno v:
The British journal of psychiatry : the journal of mental science. 114(506)
Huntington's Chorea is a hereditary neurological disease which occurs in adulthood and manifests itself in involuntary bodily movements and progressive physical and mental deterioration. It is irreversible and responds to no therapy. Its course is ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea7cc32b0a469bc90afc28b4ac37d55
https://pubmed.ncbi.nlm.nih.gov/4229842
https://pubmed.ncbi.nlm.nih.gov/4229842
Publikováno v:
Neurology. 36:1478-1478
Brain tissue was obtained promptly after death from a patient with autosomal dominant olivoponto-cerebellar atrophy and studied by immunocytochemistry and a Golgi technique. Antiglutamic acid decarboxylase showed severe loss of Purkinje cells and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5da43927bc0ba9213b583b1b8f10bc2f
https://doi.org/10.1212/wnl.36.11.1478
https://doi.org/10.1212/wnl.36.11.1478
Autor:
Mary B. Hans, Arnulf H. Koeppen
Publikováno v:
Neurology. 26:764-764
Autosomal dominant olivopontocerebellar degeneration was diagnosed in a family of Scottish ancestry by clinical examination and autopsy. In addition to having progressive cerebellar ataxia, head titubation, and severe dysarthria, the patients are una
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d000be965cac9d245d150777101e5466
https://doi.org/10.1212/wnl.26.8.764
https://doi.org/10.1212/wnl.26.8.764