Zobrazeno 1 - 10
of 599
pro vyhledávání: '"W, Schlote"'
Autor:
W. Schlote
Publikováno v:
Zeitschrift für Tierzüchtung und Züchtungsbiologie. 89:265-279
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c2033a5a15f680d4901b5f80e5b0d9c
https://doi.org/10.1111/j.1439-0388.1972.tb01405.x
https://doi.org/10.1111/j.1439-0388.1972.tb01405.x
Publikováno v:
Ultrastructural Pathology. 30:387-391
The ultrastructure of lipofuscin (Lf) was studied in hippocampal and neocortical neurons of children and youngsters between 3 months and 24 years of age. As a standard, regions CA1 and CA4 of Ammon's horn and the gyrus centralis anterior of the left
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::536dced823f0e54aa6dec4286c1c57f4
https://doi.org/10.1080/01913120600854137
https://doi.org/10.1080/01913120600854137
Autor:
R. Nafe, W. Schlote
Publikováno v:
Neuropathology and Applied Neurobiology. 30:315-328
In this review, the results of previous histomorphometric studies of brain tumours are summarized and discussed with respect to their potential value for diagnostic purposes and for tumour research. In the majority of these studies, human gliomas wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c62e68bb6430957de5af655e82245c6b
https://doi.org/10.1111/j.1365-2990.2004.00596.x
https://doi.org/10.1111/j.1365-2990.2004.00596.x
Publikováno v:
Ultrastructural Pathology. 28:341-351
Lipofuscin represents an integral part of neurons and glial cells in mammals and in submammalian species. It is a special lysosomal organelle, takes part of cellular metabolism, and is a structural expression of catabolic pathways. Species-specific d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6162c2afa1b4035494506e40a430c040
https://doi.org/10.1080/019131290882330
https://doi.org/10.1080/019131290882330
Autor:
A. Sewell, V.v. Loewenich, H. Buxmann, Nigel G. Laing, W. Schlote, Kristen J. Nowak, R. Schlosser
Publikováno v:
Neuropediatrics. 32:267-270
A premature boy with a congenital form of nemaline myopathy due to mutation in the ACTA1-gene showed decreased carnitine levels in the eighth week of life. After sufficient oral carnitine substitution he improved gradually. In the first 15 months of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe41cde0bebcc6ca6a149290fea1b48
https://doi.org/10.1055/s-2001-19122
https://doi.org/10.1055/s-2001-19122
Publikováno v:
Annals of the New York Academy of Sciences. 723:480-483
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d3cc6ce2707674141b17e99872f4fce
https://doi.org/10.1111/j.1749-6632.1994.tb36783.x
https://doi.org/10.1111/j.1749-6632.1994.tb36783.x
Publikováno v:
Neurological Research. 16:59-62
We performed light microscopic examinations on 76 aneurysms from 72 patients (multiple aneurysms in four patients). The slides were stained with HE, Elastica-van-Gieson, Goldner and Prussian blue for iron. Based on morphological findings we were able
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a8a107a7e28116358fffa3e9052ce1b
https://doi.org/10.1080/01616412.1994.11740194
https://doi.org/10.1080/01616412.1994.11740194