Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("MORIMATSU Y")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 24 of 24

  • Page / 1
Export

Selection :

  • and

Histopathological study of alobar holoprosencephaly. I: Abnormal laminar architecture of the telencephalic cortexMIZUGUCHI, M; MORIMATSU, Y.Acta neuropathologica. 1989, Vol 78, Num 2, pp 176-182, issn 0001-6322Article

Histopathological study of alobar holoprosencephaly. II: Marginal glioneural heterotopia and other gliomesenchymal abnormalitiesMIZUGUCHI, M; MORIMATSU, Y.Acta neuropathologica. 1989, Vol 78, Num 2, pp 183-188, issn 0001-6322Article

CHRONIC RECURRENT DEMYELINATING ENCEPHALOMYELITIS ASSOCIATED WITH HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSISNAGASHIMA T; YAMADA K; UONO M et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 59; NO 1; PP. 25-30; BIBL. 25 REF.Article

Foamy spheroid bodies in the globus pallidus and the substantia nigra pars reticulata : an investigation on regional distribution in 56 cases without neurodegenerative diseasesARAI, N; MIZUTANI, T; MORIMATSU, Y et al.Virchows Archiv. A, Pathological anatomy and histopathology. 1993, Vol 422, Num 4, pp 307-311, issn 0174-7398Article

Clinical and neuropathological findings in severe athetoid cerebral palsy : a comparative study of Globo-Luysian and Thalamo-Putaminal groupsHAYASHI, M; SATOH, J; SAKAMOTO, K et al.Brain & development (Tokyo. 1979). 1991, Vol 13, Num 1, pp 47-51, issn 0387-7604Article

An autopsy case of atypical infantile motor neuron disease with hyaline intraneuronal inclusionsYOKOCHI, K; ODA, M; SATOH, J et al.Archives of neurology (Chicago). 1989, Vol 46, Num 1, pp 103-107, issn 0003-9942Article

Axonal polyglucosan body in the ventral posterolateral nucleus of the human thalamus in relation to ageingMIZUTANI, T; SATOH, J; MORIMATSU, Y et al.Acta neuropathologica. 1987, Vol 74, Num 1, pp 9-12, issn 0001-6322Article

A case report of infantile striatal necrosis with an acute onsetYASUKOHCHI, S; AKABANE, T; MORI, T et al.Brain & development (Tokyo. 1979). 1986, Vol 8, Num 6, pp 609-614, issn 0387-7604Article

Non-missile head injury : report of patient surviving for 6 yearsMIZUTANI, Y; HAYAKAWA, K; TAKIZAWA, T et al.Neuropathology and applied neurobiology (Print). 1990, Vol 16, Num 5, pp 431-435, issn 0305-1846Article

Neuropathological study and chemico-pathological correlation in sibling cases of Sanfilippo syndrome type BTAMAGAWA, K; MORIMATSU, Y; FUJISAWA, K et al.Brain & development (Tokyo. 1979). 1985, Vol 7, Num 6, pp 599-609, issn 0387-7604Article

A neuropathological study of a case of lupus erythematosus with choreaKUROE, K; KURAHASHI, K; NAKANO, I et al.Journal of the neurological sciences. 1994, Vol 123, Num 1-2, pp 59-63, issn 0022-510XArticle

Atypical amyotrophic lateral sclerosis with dementia mimicking frontal Pick's disease : a report of an autopsy case with a clinical course of 15 yearsTSUCHIYA, K; IKEDA, K; HAGA, C et al.Acta neuropathologica. 2001, Vol 101, Num 6, pp 625-630, issn 0001-6322Article

Collagen-encapsulated coagulation necrosis in cerebral infarcts : a pathological studyYAMAZAKI, M; NAKANO, I; MORIMATSU, Y et al.Acta neuropathologica. 1996, Vol 91, Num 1, pp 47-52, issn 0001-6322Article

Immunohistochemical expression of microtubule-associated protein 5 (MAP5) in glial cells in multiple system atrophyARAI, N; NISHIMURA, M; ODA, M et al.Journal of the neurological sciences. 1992, Vol 109, Num 1, pp 102-106, issn 0022-510XArticle

Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph diseaseKUMADA, S; HAYASHI, M; MIZUGUCHI, M et al.Acta neuropathologica. 2000, Vol 99, Num 1, pp 48-54, issn 0001-6322Article

A neuropathological study of a case of the Prader-Willi syndrome with an interstitial deletion of the proximal long arm of chromosome 15HAYASHI, M; ITOH, M; KABASAWA, Y et al.Brain & development (Tokyo. 1979). 1992, Vol 14, Num 1, pp 58-62, issn 0387-7604Article

Peculiar axonal debris with subsequent astrocytic response (foamy spheroid body) : a topographic, light microscopic, immunohistochemical and electron microscopic studyARAI, N; YAGISHITA, S; MISUGI, K et al.Virchows Archiv. A, Pathological anatomy and histopathology. 1992, Vol 420, Num 3, pp 243-252, issn 0174-7398Article

Immunohistochemical evaluation of the marbled state in childhood hypoxic encephalopathyARAKI, S; HAYASHI, M; SUZUKI, K et al.Acta neuropathologica. 1999, Vol 98, Num 3, pp 257-261, issn 0001-6322Article

Megalencephaly, hydrocephalus and cortical dysplasia in severe dwarfism mimicking leprechaunismHAYASHI, M; KURATA, K; SUZUKI, K et al.Acta neuropathologica. 1998, Vol 95, Num 4, pp 431-436, issn 0001-6322Article

Septo-optic dysplasia with cerebellar hypoplasia in Cornelia de Lange syndromeHAYASHI, M; SAKAMOTO, K; KURATA, K et al.Acta neuropathologica. 1996, Vol 92, Num 6, pp 625-630, issn 0001-6322Article

A neuropathological study of early onset cockayne syndrome with chromosomal anomaly 47XXXHAYASHI, M; HAYAKAWA, K; SUZUKI, F et al.Brain & development (Tokyo. 1979). 1992, Vol 14, Num 1, pp 63-67, issn 0387-7604Article

Paraneoplastic cortical cerebellar degeneration. A neuropathological study of an autopsy case in comparison with cortical cerebellar degeneration in alcoholicsMIZUTANI, T; MAEDA, S; HAYAKAWA, K et al.Acta neuropathologica. 1988, Vol 77, Num 2, pp 206-212, issn 0001-6322Article

Familial bulbo-spinal muscular atrophy associated with testicular atrophy and sensory neuropathy (Kennedy-Alter-Sung syndrome): autopsy case report of two brothersNAGASHIMA, T; SEKO, K; HIROSE, K et al.Journal of the neurological sciences. 1988, Vol 87, Num 2-3, pp 141-152, issn 0022-510XArticle

Neurodegeneration in hereditary nucleotide repair disordersITOH, M; HAYASHI, M; SHIODA, K et al.Brain & development (Tokyo. 1979). 1999, Vol 21, Num 5, pp 326-333, issn 0387-7604Article

  • Page / 1