D型尼曼-匹克病（新斯科舍变种）。血液、皮肤成纤维细胞和骨髓的超微结构。 - Suppr

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Type D Niemann-Pick disease (Nova Scotia variant). Ultrastructure of blood, skin fibroblasts, and bone marrow.

作者信息

Vethamany V G, Welch J P, Vethamany S K

出版信息

Arch Pathol. 1972 Jun;93(6):537-43.

PMID:4337091

Abstract

摘要

相似文献

Type D Niemann-Pick disease (Nova Scotia variant). Ultrastructure of blood, skin fibroblasts, and bone marrow.D型尼曼-匹克病（新斯科舍变种）。血液、皮肤成纤维细胞和骨髓的超微结构。

Arch Pathol. 1972 Jun;93(6):537-43.

[The Niemann-Pick cell. Aspects in optical and ultrastructural cytology].[尼曼-匹克细胞。光学和超微结构细胞学方面]

Pathol Biol (Paris). 1973 May;21(5):483-96.

Cultured skin fibroblasts in storage disorders. An analysis of ultrastructural features.储存障碍中的培养皮肤成纤维细胞。超微结构特征分析。

Am J Pathol. 1973 Oct;73(1):59-80.

Niemann-Pick disease type C. Skin biopsies in parents.

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Fine structure and histochemistry of peripheral blood cells in Niemann-Pick disease.尼曼-匹克病外周血细胞的精细结构与组织化学

Lab Invest. 1967 Aug;17(2):155-70.

[Observations on the ultrastructure of lymph nodes in Niemann-Pick disease].

Acta Morphol Acad Sci Hung. 1971;19(4):417-32.

[Iron-containing inclusions in bone marrow plasma cells in hypoplastic anemia].[再生障碍性贫血时骨髓浆细胞中的含铁包涵体]

Arkh Anat Gistol Embriol. 1973 Jun;64(6):85-93.

[Niemann-Pick disease type C in monozygotic twins].

Minerva Pediatr. 1992 Oct;44(10):491-5.

Increased expression of caveolin-1 in heterozygous Niemann-Pick type II human fibroblasts.杂合型尼曼-匹克II型人类成纤维细胞中窖蛋白-1表达增加。

Biochem Biophys Res Commun. 1997 Jul 9;236(1):189-93. doi: 10.1006/bbrc.1997.6929.

引用本文的文献

Genetic and laboratory diagnostic approach in Niemann Pick disease type C.尼曼-匹克病C型的基因与实验室诊断方法

J Neurol. 2014 Sep;261 Suppl 2(Suppl 2):S569-75. doi: 10.1007/s00415-014-7386-8.

Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type C.D型尼曼-匹克病与C型尼曼-匹克病定位于人类18号染色体的同一区域。

Am J Hum Genet. 1997 Jul;61(1):139-42. doi: 10.1086/513899.

Niemann-Pick disease type C. Pathological, histochemical, ultrastructural and biochemical studies.C型尼曼-匹克病。病理学、组织化学、超微结构及生物化学研究。

Eur J Pediatr. 1981 Jul;136(3):263-74. doi: 10.1007/BF00442993.

Lysosome lipid storage disorder in NCTR-BALB/c mice. II. Morphologic and cytochemical studies.NCTR-BALB/c小鼠的溶酶体脂质贮积症。II. 形态学和细胞化学研究。

Am J Pathol. 1982 Aug;108(2):150-9.

Niemann-Pick disease (Crocker's type C): A histological study of the distribution and qualitative differences fo the storage process.尼曼-皮克病（克罗克C型）：储存过程的分布及质性差异的组织学研究

Acta Neuropathol. 1975 Dec 19;33(3):191-200. doi: 10.1007/BF00688393.

Genetic and demographic aspects of Nova Scotia Niemann-Pick disease (type D).新斯科舍省尼曼-匹克病（D型）的遗传和人口统计学方面。

Am J Hum Genet. 1978 Sep;30(5):530-8.

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