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Ataxia-telangiectasia and Swiss-type agammaglobulinemia. Two genetic disorders of the immune mechanism in related Amish sibships.

作者信息

McKusick V A, Cross H E

出版信息

JAMA. 1966 Feb 28;195(9):739-45. doi: 10.1001/jama.195.9.739.

DOI:10.1001/jama.195.9.739
PMID:5951879
Abstract
摘要

相似文献

1
Ataxia-telangiectasia and Swiss-type agammaglobulinemia. Two genetic disorders of the immune mechanism in related Amish sibships.共济失调毛细血管扩张症和瑞士型无丙种球蛋白血症。阿米什族相关同胞中的两种免疫机制遗传性疾病。
JAMA. 1966 Feb 28;195(9):739-45. doi: 10.1001/jama.195.9.739.
2
[Immunologic study of a case of ataxia-telangiectasia and her family].
Bull Mem Soc Med Hop Paris. 1966 Mar 11;117(4):245-62.
3
Ataxia-telangiectasia: a familial degenerative disease leading to mental retardation--a case report.
Am J Ment Defic. 1966 Sep;71(2):185-90.
4
[Familial disease characterized by the association of a nonprogressive ataxic gait, palmar telangiectasis and hypogammaglobulinemia].
Arch Neurobiol (Madr). 1970 Apr-Jun;33(2):233-6.
5
[The ataxia-telangiectasis syndrome (Louis-Bar syndrome) from the immunologic viewpoint].
Helv Paediatr Acta. 1965 Jun;20(2):137-46.
6
Ataxia-telangiectasia.
Birth Defects Orig Artic Ser. 1975;11(2):408-9.
7
[ATAXIA-TELANGIECTASIS. CLINICAL AND IMMUNOLOGICAL STUDY OF A CASE].[共济失调毛细血管扩张症。一例病例的临床与免疫学研究]
Pediatrie. 1964 Sep;19:735-43.
8
ATAXIA-TELANGIECTASIA. FURTHER OBSERVATIONS AND REPORT OF EIGHT CASES.
Am J Dis Child. 1965 Jul;110:51-63.
9
[ATAXIA-TELANGIECTASIS SYNDROME WITH DILATATION OF BRONCHI AND GAMMA GLOBULIN DEFICIENCY].[伴有支气管扩张和γ球蛋白缺乏的共济失调-毛细血管扩张综合征]
Arch Fr Pediatr. 1964 Dec;21:1213-6.
10
Patterns of mortality in the the Old Order Amish. I. Background and major causes of death.旧秩序阿米什人的死亡模式。一、背景与主要死因。
Am J Epidemiol. 1981 Dec;114(6):845-61. doi: 10.1093/oxfordjournals.aje.a113255.

引用本文的文献

1
Low cancer incidence rates in Ohio Amish.俄亥俄州阿米什人癌症发病率较低。
Cancer Causes Control. 2010 Jan;21(1):69-75. doi: 10.1007/s10552-009-9435-7. Epub 2009 Sep 25.
2
Genetic and biochemical studies with ataxia telangiectasia. A review.共济失调毛细血管扩张症的遗传学和生物化学研究。综述。
Hum Genet. 1981;59(1):1-9. doi: 10.1007/BF00278846.
3
An unusual case of metaphyseal chondrodysplasia with an abnormal perilacunar matrix associated with agranulocytosis and hypoplasia of the thymus.一例罕见的干骺端软骨发育异常病例,伴有异常的陷窝周围基质,与粒细胞缺乏症和胸腺发育不全相关。
Virchows Arch A Pathol Anat Histol. 1981;391(3):275-89. doi: 10.1007/BF00709160.
4
Epstein-Barr virus (EBV), lymphocytes and transformation.爱泼斯坦-巴尔病毒(EBV)、淋巴细胞与转化
J Cancer Res Clin Oncol. 1983;106(1):1-11. doi: 10.1007/BF00399890.
5
[Ataxia-telangiectasia (Louis-Bar-syndrome). Report on seven cases].
Z Kinderheilkd. 1970;107(4):324-42. doi: 10.1007/BF00438894.
6
Cytogenetic study of patients with ataxia-telangiectasia.
Humangenetik. 1974;24(2):115-28. doi: 10.1007/BF00283768.
7
The incidence and gene frequency of ataxia-telangiectasia in the United States.美国共济失调毛细血管扩张症的发病率和基因频率。
Am J Hum Genet. 1986 Nov;39(5):573-83.
8
The differential diagnosis of the short-limbed dwarfs presenting at birth.
Postgrad Med J. 1977 Apr;53(618):204-11. doi: 10.1136/pgmj.53.618.204.
9
Metaphyseal chondrodysplasia.干骺端软骨发育异常
Postgrad Med J. 1977 Aug;53(622):480-7. doi: 10.1136/pgmj.53.622.480.