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Studies on adult metachromatic leukodystrophy. 1. Clinical, morphological and histochemical observations in two cases.

作者信息

Müller D, Pilz H, ter Meulen V

出版信息

J Neurol Sci. 1969 Nov-Dec;9(3):567-84. doi: 10.1016/0022-510x(69)90095-1.

DOI:10.1016/0022-510x(69)90095-1
PMID:4189441
Abstract
摘要

相似文献

1
Studies on adult metachromatic leukodystrophy. 1. Clinical, morphological and histochemical observations in two cases.
J Neurol Sci. 1969 Nov-Dec;9(3):567-84. doi: 10.1016/0022-510x(69)90095-1.
2
Leukodystrophy: diffuse cerebral sclerosis or Schilder's disease revisited.脑白质营养不良：再探弥漫性脑硬化或席尔德病。
Perspect Pediatr Pathol. 1975;2:61-100.
3
[Histochemical study on a case of metachromatic leukodystrophy].
Pathol Eur. 1968;3(2):313-22.
4
[Amaurotic idiocy connected with metachromatic leukodystrophy: transitional form or combination? Electron microscopic and histochemical finding].[与异染性脑白质营养不良相关的黑蒙性白痴：过渡形式还是合并症？电子显微镜和组织化学研究结果]
Acta Neuropathol. 1967 May 5;8(3):292-308. doi: 10.1007/BF00688830.
5
Comparative histological and histochemical studies of infantile and adult metachromatic leucodystrophy.
Pathol Eur. 1968;3(2):286-93.
6
[Autopsy case of late-life nonmetachromatic leukodystrophy].[老年期异染性脑白质营养不良尸检病例]
No To Shinkei. 1967 Aug;19(8):835-42.
7
The reliability of the diagnosis of metachromatic leucodystrophy by peripheral nerve biopsy.通过周围神经活检诊断异染性脑白质营养不良的可靠性。
Acta Paediatr Scand. 1969 Jan;58(1):15-24. doi: 10.1111/j.1651-2227.1969.tb04324.x.
8
Further observations on the fine structure of globoid leukodystrophy. Peripheral neuropathy and optic nerve involvement.球形细胞脑白质营养不良的精细结构的进一步观察。周围神经病变和视神经受累。
Hum Pathol. 1972 Sep;3(3):371-88. doi: 10.1016/s0046-8177(72)80038-8.
9
Peripheral neuropathy of metachromatic leucodystrophy: observations on segmental demyelination and remyelination and the intracellular distribution of sulphatide.异染性脑白质营养不良的周围神经病：节段性脱髓鞘和再髓鞘形成以及硫脂细胞内分布的观察
J Neurol Neurosurg Psychiatry. 1967 Aug;30(4):311-8. doi: 10.1136/jnnp.30.4.311.
10
The late form of metachromatic leukodystrophy. II. Ultrastructural correlations with morphological and neurochemical findings.异染性脑白质营养不良的晚期形式。II. 与形态学和神经化学发现的超微结构相关性
J Neurol Sci. 1972 Dec;17(4):383-7. doi: 10.1016/0022-510x(72)90150-5.

引用本文的文献

1
Metachromatic leukodystrophy: a case of triplets with the late infantile variant and a systematic review of the literature.异染性脑白质营养不良：一例三胞胎患晚发性婴儿型变异型病例及文献系统综述
J Child Neurol. 2010 May;25(5):572-80. doi: 10.1177/0883073809341669. Epub 2009 Dec 28.
2
Late onset phenylalanine intoxication.迟发性苯丙氨酸中毒。
J Inherit Metab Dis. 1980;2(1):19-20. doi: 10.1007/BF01805558.
3
A preclinical case of late adult metachromatic leukodystrophy? Manifestation only with lipid abnormalities in urine, enzyme deficiency and decrease of nerve conduction velocity.
晚期成人异染性脑白质营养不良的一例临床前病例？仅表现为尿中脂质异常、酶缺乏和神经传导速度降低。
J Neurol Neurosurg Psychiatry. 1972 Jun;35(3):360-4. doi: 10.1136/jnnp.35.3.360.
4
[Clinical and histological diagnosis of a case of familial adult metachromatic leucodystrophy (author's transl)].一例家族性成人异染性脑白质营养不良的临床及组织学诊断（作者译）
J Neurol. 1974;207(3):189-204. doi: 10.1007/BF00312560.
5
The fatty acid composition of cerebrosides and sulfatides in a case of adult metachromatic leukodystrophy.一例成人异染性脑白质营养不良患者中脑苷脂和硫脂的脂肪酸组成
Z Neurol. 1974 Mar 29;206(3):203-8. doi: 10.1007/BF00316534.
6
[Metachromatic leukodystrophy (sulfatide lipidosis) in adults: intravital diagnosis in two patients with clinical symptoms of presenile atrophy of the brain].
Z Neurol. 1971;199(3):234-55.
7
Four cases of late onset metachromatic leucodystrophy in a family: clinical, biochemical and neuropathological studies.一个家族中的4例迟发性异染性脑白质营养不良：临床、生化及神经病理学研究
J Neurol Neurosurg Psychiatry. 1986 Dec;49(12):1417-22. doi: 10.1136/jnnp.49.12.1417.
8
Metachromatic leukodystrophy: conduct disorder progressing to dementia.异染性脑白质营养不良：品行障碍进展为痴呆。
J Neurol Neurosurg Psychiatry. 1987 Apr;50(4):488-9. doi: 10.1136/jnnp.50.4.488.
9
Adult-onset metachromatic leucodystrophy presenting without psychiatric symptoms.
J Neurol. 1989 Oct;236(7):427-9. doi: 10.1007/BF00314905.
10
Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.不同程度芳基硫酸酯酶A缺乏症的基因型与表型关系
Hum Genet. 1991 Mar;86(5):463-70. doi: 10.1007/BF00194634.