Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kay W. Nolte"'
Autor:
Ahmet Parlak, Christian-Andreas Mueller, Kay W. Nolte, Tobias P. Schmidt, Ulf Bertram, Hans Clusmann, Christian Blume
Publikováno v:
Brain and Spine, Vol 4, Iss , Pp 103325- (2024)
Introduction: IgG4-related disease is an immune-mediated condition characterized by tissue infiltration of IgG4-positive plasma cells. Involvement of the spinal meninges results in hypertrophic spinal pachymeningitis (HSP), causing spinal cord and ne
Externí odkaz:
https://doaj.org/article/b976a179a64d423aa2ebb9549b7aef22
Autor:
Lisa Kabelitz, Andrea Nonn, Kay W Nolte, Omid Nikoubashman, Ahmed Othman, Sarah Heringer, Martin Kramer, Martin Wiesmann, Marc A Brockmann
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0163878 (2016)
Minipigs are frequently used in (neuro-)interventional research. Longitudinal experiments may require repeated vessel access via the femoral artery. Anticoagulation and incompliance of the animals necessitates the use of a vascular closure device (VC
Externí odkaz:
https://doaj.org/article/ad8e083a982b45a4911347e835ba0e59
Autor:
Kay W, Nolte, Sonja, Trepels-Kottek, Dagmar, Honnef, Joachim, Weis, Christian G, Bien, Andreas, van Baalen, Klaus, Ritter, Birgit, Czermin, Sabine, Rudnik-Schöneborn, Norbert, Wagner, Martin, Häusler
Publikováno v:
Neuropathology : official journal of the Japanese Society of Neuropathology. 33(1)
Mutations affecting the mitochondrial DNA-polymerase gamma 1 (POLG1) gene have been shown to cause Alpers-Huttenlocher disease. Ultrastructural data on brain and muscle tissue are rare. We report on ultrastructural changes in brain and muscle tissue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::539e6ef8238cddfbc5df34444e8ffe0f
https://pubmed.ncbi.nlm.nih.gov/22537151
https://pubmed.ncbi.nlm.nih.gov/22537151
Autor:
Kathleen, Parthey, Malte, Kornhuber, Christian, Kunze, Dorothea, Wand, Kay W, Nolte, Stefan, Nikolin, Joachim, Weis, J Michael, Schröder
Publikováno v:
Musclenerve. 45(2)
In this study we describe a case of a term infant with the neurological variant of Waardenburg syndrome type 4 (i.e., PCWH = peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5e62db89db39575201287c7d4808d5b8
https://pubmed.ncbi.nlm.nih.gov/22246888
https://pubmed.ncbi.nlm.nih.gov/22246888