[Addison's disease without increase of pigmentation (so-called white Addison's disease)].
作者信息
HEDINGER C
出版信息
Schweiz Med Wochenschr. 1950 May 13;80(19):489-91.
PMID:15418154
Abstract
摘要
相似文献
1
[Addison's disease without increase of pigmentation (so-called white Addison's disease)].[无色素沉着增加的艾迪生病（所谓的白色艾迪生病）]
Schweiz Med Wochenschr. 1950 May 13;80(19):489-91.
2
[Pigmentation as sole symptom of Addison's disease].[色素沉着作为艾迪生病的唯一症状]
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[Addison's disease].[艾迪生病]
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4
[On Addison's disease without pigmentation].[关于无色素沉着的艾迪生病]
Probl Endokrinol Gormonoter. 1960 Jul-Aug;6:37-41.
5
[On the problem of Addison's disease without pigmentation].[关于无色素沉着的艾迪生病问题]
Suvr Med (Sofiia). 1960;11(10):48-54.
6
[The problem of lingual pigmentation in Addison's disease].[艾迪生病中的舌色素沉着问题]
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7
Addison's disease presenting as loss of weight without pigmentation.表现为体重减轻且无色素沉着的艾迪生病。
Proc R Soc Med. 1955 Dec;48(12):1023-4. doi: 10.1177/003591575504801208.
8
[Pigmentation in Addison's disease; clinical bases for a new conception].[艾迪生病中的色素沉着；一种新概念的临床依据]
Presse Med (1893). 1953 Feb 25;61(13):263-6.
9
CRISIS FOLLOWING CORTICOTROPHIN IN ADDISON'S DISEASE WITHOUT PIGMENTATION.无色素沉着的艾迪生病患者使用促肾上腺皮质激素后的危象
Postgrad Med J. 1964 Jan;40(459):26-8. doi: 10.1136/pgmj.40.459.26.
10
PIGMENTATION AS THE PRESENTING FEATURE OF ADDISON'S DISEASE: REPORT OF A CASE.色素沉着作为艾迪生病的首发症状：一例报告
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An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W).一个非同寻常的家族性糖皮质激素缺乏症病例，其特征为 MC2R（T152K）和 MC1R（R160W）共存纯合突变，无色素沉着。
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