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SCHILDER'S DISEASE (SUDANOPHILIC LEUCODYSTROPHY) IN FIVE MALE MEMBERS OF ONE FAMILY.

作者信息

CROME L, ZAPELLA M

出版信息

J Neurol Neurosurg Psychiatry. 1963 Oct;26(5):431-8. doi: 10.1136/jnnp.26.5.431.

DOI:10.1136/jnnp.26.5.431
PMID:14066635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC495612/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/66fc37ebb09d/jnnpsyc00263-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/ff283fa85eb2/jnnpsyc00263-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/ca1d3d62831f/jnnpsyc00263-0049-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/bb6e01b55acb/jnnpsyc00263-0049-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/b1b2ab817d9d/jnnpsyc00263-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/66fc37ebb09d/jnnpsyc00263-0050-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/ff283fa85eb2/jnnpsyc00263-0049-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/ca1d3d62831f/jnnpsyc00263-0049-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/bb6e01b55acb/jnnpsyc00263-0049-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/b1b2ab817d9d/jnnpsyc00263-0050-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0492/495612/66fc37ebb09d/jnnpsyc00263-0050-b.jpg

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SCHILDER'S DISEASE (SUDANOPHILIC LEUCODYSTROPHY) IN FIVE MALE MEMBERS OF ONE FAMILY.
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Curr Neurol Neurosci Rep. 2014 Oct;14(10):486. doi: 10.1007/s11910-014-0486-0.
2
[LEUKODYSTROPHY WITH ORTHOCHROMATIC BREAKDOWN PRODUCTS. A CONTRIBUTION TO PELIZAEUS-MERZBACHER DISEASE].[伴有正染性崩解产物的脑白质营养不良。对佩利措伊斯-梅茨巴赫病的一项贡献]
Virchows Arch Pathol Anat Physiol Klin Med. 1965 Feb 15;338:371-94.
3
Adrenoleukodystrophy--its diverse CT appearances and an evolutive or phenotypic variant: the leukodystrophy without adrenal insufficiency.

本文引用的文献

1
A case of central neurofibromatosis.一例中枢神经纤维瘤病。
Arch Dis Child. 1962 Dec;37(196):640-51. doi: 10.1136/adc.37.196.640.
2
[A familial syndrome with diffuse degenerative sclerosis (Pelizaeus-Merzbacher type), tapetoretinal degeneration & dwarfism; preliminary report].
Ophthalmologica. 1959 Mar;137(3):147-54. doi: 10.1159/000303504.
3
Natural history and evolution of the concept of Schilder's diffuse sclerosis.希尔德弥漫性硬化概念的自然史与演变
Acta Psychiatr Neurol Scand. 1956;31(3):285-331. doi: 10.1111/j.1600-0447.1956.tb09694.x.
肾上腺脑白质营养不良——其多样的CT表现及一种演变型或表型变异：无肾上腺功能不全的脑白质营养不良。
Neuroradiology. 1982;24(1):33-42. doi: 10.1007/BF00344581.
4
Macrophages migration through the brain parenchyma to the perivascular space following particle ingestion.巨噬细胞在摄取颗粒后穿过脑实质迁移至血管周围间隙。
Am J Pathol. 1978 Oct;93(1):153-64.
5
Myelin deficiency (md): a neurologic mutant in the Wistar rat.髓磷脂缺乏症（md）：Wistar大鼠中的一种神经学突变体。
Am J Pathol. 1979 Apr;95(1):215-24.
4
[Merzbacher-Pelizaeus disease; clinico-anatomic studies of its position among the diffuse scleroses].
Wien Z Nervenheilkd Grenzgeb. 1954;9(3):228-89.
5
A histological and chemical study of three cases of diffuse cerebral sclerosis.三例弥漫性脑硬化的组织学与化学研究
J Neurol Neurosurg Psychiatry. 1954 Feb;17(1):33-49. doi: 10.1136/jnnp.17.1.33.