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Cerebral lesions in familial amyotrophic lateral sclerosis and dementia.

作者信息

Finlayson M H, Martin J B

出版信息

Acta Neuropathol. 1973 Nov 5;26(3):237-46. doi: 10.1007/BF00684433.

DOI:10.1007/BF00684433
PMID:4769153
Abstract
摘要

相似文献

1
Cerebral lesions in familial amyotrophic lateral sclerosis and dementia.家族性肌萎缩侧索硬化症与痴呆中的脑损伤
Acta Neuropathol. 1973 Nov 5;26(3):237-46. doi: 10.1007/BF00684433.
2
[Hippocampal pathology in dementia patients with amyotrophic lateral sclerosis].
No To Shinkei. 1998 Oct;50(10):915-22.
3
Familial amyotrophic lateral sclerosis with dementia: a second canadian family.伴有痴呆的家族性肌萎缩侧索硬化症:第二个加拿大家庭
Clin Genet. 1975 Mar;7(3):186-91. doi: 10.1111/j.1399-0004.1975.tb00317.x.
4
[A case of Pick's disease with terminal amyotrophic lateral sclerosis. Contribution to the temporal semiology].[一例伴有终末期肌萎缩侧索硬化的匹克氏病。对颞叶症状学的贡献]
Rev Neurol (Paris). 1967 May;116(5):373-82.
5
Cerebral cortical and white matter lesions in amyotrophic lateral sclerosis with dementia: correlation with MR and pathologic examinations.肌萎缩侧索硬化症合并痴呆患者的大脑皮质和白质病变:与磁共振成像及病理检查的相关性
AJNR Am J Neuroradiol. 2007 Sep;28(8):1505-10. doi: 10.3174/ajnr.A0605.
6
[Amyotrophic lateral sclerosis with dementia].[伴有痴呆的肌萎缩侧索硬化症]
Ryoikibetsu Shokogun Shirizu. 1999(27 Pt 2):326-9.
7
Familial amyotrophic lateral sclerosis and parkinsonism-dementia complex of the Kii Peninsula of Japan: clinical and neuropathological study and tau analysis.日本纪伊半岛的家族性肌萎缩侧索硬化症和帕金森病-痴呆综合征:临床与神经病理学研究及tau分析。
Ann Neurol. 2001 Apr;49(4):501-11.
8
[Semantic dementia associated with amyotrophic lateral sclerosis].[与肌萎缩侧索硬化相关的语义性痴呆]
Rev Neurol (Paris). 2009 Mar;165(3):278-81. doi: 10.1016/j.neurol.2008.06.008. Epub 2008 Aug 28.
9
Neuroradiological study of patients with amyotrophic lateral sclerosis and parkinsonism-dementia complex on the Kii peninsula of Japan.对日本纪伊半岛肌萎缩侧索硬化症和帕金森病-痴呆综合征患者的神经放射学研究。
Arch Neurol. 2003 Sep;60(9):1257-61. doi: 10.1001/archneur.60.9.1257.
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Amyotrophic lateral sclerosis and frontal lobe dementia in Alzheimer's disease. Case report and review of the literature.
Eur Neurol. 1993;33(4):320-4. doi: 10.1159/000116962.

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Cognitive and behavioral involvement in ALS has been known for more than a century.肌萎缩侧索硬化症的认知和行为参与已经有一个多世纪的历史了。
Neurol Sci. 2022 Dec;43(12):6741-6760. doi: 10.1007/s10072-022-06340-0. Epub 2022 Sep 2.
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Comparative analysis of C9orf72 and sporadic disease in an ALS clinic population.肌萎缩侧索硬化症(ALS)临床患者群体中C9orf72与散发性疾病的对比分析。
Neurology. 2016 Sep 6;87(10):1024-30. doi: 10.1212/WNL.0000000000003067. Epub 2016 Aug 3.
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Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.

本文引用的文献

1
Epidemiologic investigations of amyotrophic lateral sclerosis. 2. Familial aggregations indicative of dominant inheritance. I.肌萎缩侧索硬化症的流行病学调查。2. 提示显性遗传的家族聚集性。I
Neurology. 1955 Mar;5(3):182-96. doi: 10.1212/wnl.5.3.182.
2
SOVIET SEARCH FOR VIRUSES THAT CAUSE CHRONIC NEUROLOGIC DISEASES IN THE U.S.S.R.苏联对苏联境内导致慢性神经疾病的病毒的研究
Science. 1965 Mar 5;147(3662):1114-6. doi: 10.1126/science.147.3662.1114.
3
STUDY OF THE ETIOLOGY OF AMYOTROPHIC LATERAL SCLEROSIS.肌萎缩侧索硬化症病因研究
建立联系:病理学和遗传学将肌萎缩侧索硬化症与额颞叶痴呆联系起来。
J Mol Neurosci. 2011 Nov;45(3):663-75. doi: 10.1007/s12031-011-9637-9. Epub 2011 Sep 7.
4
Motor neuron disease and frontotemporal dementia: One, two, or three diseases?运动神经元病与额颞叶痴呆:一种、两种还是三种疾病?
Ann Indian Acad Neurol. 2010 Dec;13(Suppl 2):S81-8. doi: 10.4103/0972-2327.74250.
5
Dementia of frontal type and dementias with subcortical gliosis.额颞叶型痴呆及伴有皮质下胶质增生的痴呆
Brain Pathol. 1998 Apr;8(2):325-38. doi: 10.1111/j.1750-3639.1998.tb00157.x.
6
Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles.伴有超氧化物歧化酶-1(SOD-1)点突变的家族性肌萎缩侧索硬化症:与神经原纤维缠结相关的疾病持续时间的家族内异质性。
J Neurol Neurosurg Psychiatry. 1995 Sep;59(3):266-70. doi: 10.1136/jnnp.59.3.266.
7
Presenile dementia with motor neuron disease in Japan: clinico-pathological review of 26 cases.日本的早老性痴呆伴运动神经元病:26例临床病理回顾
J Neurol Neurosurg Psychiatry. 1984 Sep;47(9):953-9. doi: 10.1136/jnnp.47.9.953.
8
Frontal lobe dementia and motor neuron disease.额颞叶痴呆和运动神经元病。
J Neurol Neurosurg Psychiatry. 1990 Jan;53(1):23-32. doi: 10.1136/jnnp.53.1.23.
Bull World Health Organ. 1963;29(4):449-56.
4
NEURONAL ENZYMATIC FAILURE IN CREUTZFELDT-JAKOB DISEASE; A FAMILIAL STUDY.
Arch Neurol. 1964 Feb;10:181-95. doi: 10.1001/archneur.1964.00460140067009.
5
[CLINICAL AND ANATOMOPATHOLOGICAL STUDIES ON COMBINED FORMS OF PRESENILE BRAIN ATROPHY (PICK, ALZHEIMER) WITH ATROPHYING SPINAL PROCESSES].[早老性脑萎缩(匹克氏病、阿尔茨海默病)合并脊髓萎缩病变的临床及解剖病理学研究]
Psychiatr Neurol (Basel). 1963;145:322-44.
6
[On intracellular inclusions in familial amyotrophic lateral sclerosis].[关于家族性肌萎缩侧索硬化症中的细胞内包涵体]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1962;62:1293-9.
7
Alzheimer's neurofibrillary changes. A topographic study.阿尔茨海默病神经纤维变化。一项地形学研究。
Arch Neurol. 1962 Sep;7:227-42. doi: 10.1001/archneur.1962.04210030065009.
8
Parkinsonism-dementia complex, an endemic disease on the island of Guam. II. Pathological features.帕金森病痴呆综合征,关岛岛上的一种地方病。II. 病理特征。
Brain. 1961 Dec;84:662-79. doi: 10.1093/brain/84.4.662.
9
[Typical amyotrophic lateral sclerosis and hereditary paralysis agitans in the same family with the possibility of a form transitional between the two].[同一家族中典型的肌萎缩侧索硬化症和遗传性帕金森震颤麻痹,两者之间可能存在一种过渡形式]
Monatsschr Psychiatr Neurol. 1954 Apr-May;127(4-5):185-203.
10
Progressive bulbar paralysis showing heredofamilial incidence and intellectual impairment.
AMA Arch Neurol Psychiatry. 1953 Feb;69(2):196-207.