Found: 13
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Epidemiology of X-linked adrenoleukodystrophy in Japan.
- Published in:
- Journal of Human Genetics, 2002, v. 47, n. 11, p. 590, doi. 10.1007/s100380200090
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- Publication type:
- Article
Interplay of (inter)subjectivity and social norm.
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- Journal of Historical Pragmatics, 2007, v. 8, n. 2, p. 239, doi. 10.1075/jhp.8.2.05ono
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- Publication type:
- Article
Historical changes in Japanese: With special focus on subjectivity and intersubjectivity: Introduction.
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- Journal of Historical Pragmatics, 2007, v. 8, n. 2, p. 153, doi. 10.1075/jhp.8.2.02ono
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- Publication type:
- Article
Morphological characterisation of glial and neuronal tau pathology in globular glial tauopathy (Types II and III).
- Published in:
- Neuropathology & Applied Neurobiology, 2020, v. 46, n. 4, p. 344, doi. 10.1111/nan.12581
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- Publication type:
- Article
Co-occurrence of argyrophilic grain disease in sporadic amyotrophic lateral sclerosis.
- Published in:
- Neuropathology & Applied Neurobiology, 2012, v. 38, n. 1, p. 54, doi. 10.1111/j.1365-2990.2011.01175.x
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- Publication type:
- Article
Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations.
- Published in:
- 2008
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- Publication type:
- Journal Article
Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.
- Published in:
- 2011
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- Publication type:
- Journal Article
TDP-43 mutation in familial amyotrophic lateral sclerosis.
- Published in:
- 2008
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- Publication type:
- journal article
A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.
- Published in:
- 2005
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- Publication type:
- Journal Article
SCA17 hemozygote showing Huntington's disease-like phenotype.
- Published in:
- 2004
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- Publication type:
- Journal Article
Elevated serum pentraxin 3 levels might predict the diagnosis of branch atheromatous disease at a very early stage.
- Published in:
- European Journal of Neurology, 2020, v. 27, n. 7, p. 1279, doi. 10.1111/ene.14249
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- Publication type:
- Article
Diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia due to CSF1R mutation.
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- European Journal of Neurology, 2018, v. 25, n. 1, p. 142, doi. 10.1111/ene.13464
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- Publication type:
- Article
Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation.
- Published in:
- European Journal of Neurology, 2017, v. 24, n. 1, p. 37, doi. 10.1111/ene.13125
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- Publication type:
- Article