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Volumn 52, Issue 11, 2012, Pages 1383-1385

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): Its clinical concept and the review of the previously reported cases

Author keywords

Axonal spheroid; Cognitive decline; Hereditary leukoencephalopathy; Pre senile dementia

Indexed keywords

ADOLESCENT; ADULT; AGED; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CLINICAL FEATURE; CONFERENCE PAPER; DEMENTIA; DIFFERENTIAL DIAGNOSIS; GENETIC DISORDER; HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH AXONAL SPHEROID; HUMAN; LEUKODYSTROPHY; LEUKOENCEPHALOPATHY; PRESENILE DEMENTIA; SCHOOL CHILD; SPHEROID CELL; WHITE MATTER;

EID: 84880557426     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.52.1383     Document Type: Conference Paper
Times cited : (7)

References (9)
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  • 2
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    • Peiffer, J.1
  • 4
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    • Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy. A single entity?
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    • (2009) Neurology , vol.72 , pp. 1953-1959
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  • 5
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    • Adult pigmentary type (Peiffer) of sudanophilic leukodystrophy: Pathological and morphometrical studies on two autopsy cases of siblings
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  • 6
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    • Long tract degeneration in familial sudanophilic leukodystrophy with prominent spheroids
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  • 7
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    • An autopsy case of hereditary diffuse leukodystrophy with spheroids, clinically suspected of Alzheimer's disease
    • Terada S, Ishizu H, Yokota O, et al. An autopsy case of hereditary diffuse leukodystrophy with spheroids, clinically suspected of Alzheimer's disease. Acta Neuropathol 2004;108:538-545.
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  • 8
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    • Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: Clinical and neuropathological characteristics
    • Itoh K, Shiga K, Shimizu K, et al. Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics. Acta Neuropathol 2006;111:39-45.
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  • 9
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    • Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
    • Randemarkers R, Baker M, Nicholson AM, et al. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nat Genet 2012;44:200-207.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.