[A complex abiotrophy: from hereditary ataxia to acropathia ulcero-mutilans].
作者信息
Bugiani O, van Bogaert L
出版信息
Acta Neurol (Napoli). 1967 Mar-Apr;22(2):238-9.
PMID:5606828
Abstract
摘要
相似文献
1
[A complex abiotrophy: from hereditary ataxia to acropathia ulcero-mutilans].[一种复杂的营养缺乏症：从遗传性共济失调到溃疡性致残性肢端病]
Acta Neurol (Napoli). 1967 Mar-Apr;22(2):238-9.
2
[Acropathia ulcero-mutilans].[肢端溃疡性坏疽]
Cah Coll Med Hop Paris. 1968 Feb;9(2):145-54.
3
[Acropathia ulcero-mutilans: its association with pellagra].
Arch Argent Dermatol. 1968 Mar;18(1):57-70.
4
[Acropathia ulcero-mutilans of sporadic form. Association with dementia. Case report].[散发性肢端溃疡型坏疽。与痴呆的关联。病例报告]
J Med Lyon. 1969 Apr 5;50(162):607-11.
5
[Thevenard's acropathia ulcero-mutilans. (Nosography and clinical case report)].[特韦纳尔氏溃疡性致残性肢端病。（疾病分类学与临床病例报告）]
Acta Neurol (Napoli). 1968 Mar-Apr;23(2):308-20.
6
[A case of familial ulcero-mutilans acropathia with trigger factor in a paradiabetic and demented patient].[一例伴有触发因素的家族性肢端溃疡型坏疽病，患者患有糖尿病前期和痴呆症]
J Med Lyon. 1970 Apr 5;51(184):917-22.
7
[Familial disease with ulcero-mutilans acropathia, pyramidal syndrome and debility].[伴有肢端溃疡-残毁性病变、锥体束综合征和虚弱的家族性疾病]
J Med Lyon. 1970 Apr 5;51(184):925-35.
8
[Acropathia ulcero-mutilans: pure osseous form with copious outgrowth reaction].[溃疡性致残性肢端病：伴有大量增生反应的纯骨型]
Rev Rhum Mal Osteoartic. 1969 Jun;36(6):328-32.
9
[Acropathia ulcero-mutilans of the lower extremities with acute and unusual radiological evolution].[伴有急性和异常放射学演变的下肢溃疡性致残性肢端病]
Bull Soc Fr Dermatol Syphiligr. 1967;74(5):673-5.
10
[A case of nonfamilial ulcero-mutilans acropathy].[一例非家族性肢端溃疡坏疽性病变]
J Radiol Electrol Med Nucl. 1972 Aug-Sep;53(8):674.
引用本文的文献
1
Ulcero-mutilating acropathy, hereditary sensory neuropathy and signs of Friedreich heredo-ataxia in two brothers.
Humangenetik. 1971;12(1):81-2. doi: 10.1007/BF00291040.
Zotero 插件