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Volume 107, Number 5, May 2004

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An isomorphic subtype of long-term epilepsy-associated astrocytomas associated with benign prognosis
pp. 381-388(8)
Authors: Blümcke, Ingmar; Luyken, Cordelia; Urbach, Horst; Schramm, Johannes; Wiestler, Otmar

Glial reactions and the clearance of amyloid  protein in the brains of patients with hereditary cerebral hemorrhage with amyloidosis-Dutch type
pp. 389-398(10)
Authors: Maat-Schieman, Marion; Yamaguchi, Haruyasu; Hegeman-Kleinn, Ingrid; Welling-Graafland, Corrie; Natté, Remco; Roos, Raymund; Duinen, Sjoerd

Increased expression of neuronal cyclooxygenase-2 in the hippocampus in amyotrophic lateral sclerosis both with and without dementia
pp. 399-405(7)
Authors: Yokota, Osamu; Terada, Seishi; Ishizu, Hideki; Ishihara, Takeshi; Nakashima, Hanae; Kugo, Aki; Tsuchiya, Kuniaki; Ikeda, Kenji; Hayabara, Toshiyuki; Saito, Yuko; Murayama, Shigeo; Uéda, Kenji; Checler, Frédéric; Kuroda, Shigetoshi

The beneficial effect of mild hypothermia in a rat model of repeated thromboembolic insults
pp. 413-420(8)
Authors: Urrea, Carlos; Danton, Gary; Bramlett, Helen; Dietrich, W.

Relationships between ultrastructural scrapie pathology and patterns of abnormal prion protein accumulation
pp. 428-438(11)
Authors: Ersdal, Cecilie; Simmons, Marion; González, Lorenzo; Goodsir, Caroline; Martin, Stuart; Jeffrey, Martin

Ultrastructural detection of DNA fragmentation in myonuclei of fatal reducing body myopathy
pp. 439-442(4)
Authors: Ikezoe, Koji; Nakagawa, Masahiro; Osoegawa, Manabu; Kira, Jun-ichi; Nonaka, Ikuya

Relative expression of human telomerase catalytic subunit (hTERT) transcripts in astrocytic gliomas
pp. 443-451(9)
Authors: Kotoula, V.; Barbanis, S.; Nikolakaki, E.; Koufoyannis, D.; Papadimitriou, C.; Karkavelas, G.

Slow component of axonal transport is impaired in the proximal axon of transgenic mice with a G93A mutant SOD1 gene
pp. 452-460(9)
Authors: Sasaki, Shoichi; Warita, Hitoshi; Abe, Koji; Iwata, Makoto

Ultrastructural study of mitochondria in the spinal cord of transgenic mice with a G93A mutant SOD1 gene
pp. 461-474(14)
Authors: Sasaki, Shoichi; Warita, Hitoshi; Murakami, Tetsuro; Abe, Koji; Iwata, Makoto

Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion
pp. 475-478(4)
Authors: García-Cabezas, M.; García-Alix, A.; Martín, Y.; Gutiérrez, M.; Hernández, C.; Rodríguez, J.; Morales, C.

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