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Subject Index Vol. 29, 2010

Autor: Christopher F. Bladin, D. Dormont, Masafumi Harada, Astrid M. Vicente, Kenneth Butcher, Delphine Michel-Monigadon, Kristina Szabo, Sofia A. Oliveira, Marta Rubiera, Heinz G. Endres, Jeroen Hendrikse, Sophie Domingues-Montanari, Klaus Berger, S. Crozier, Marc Ribó, Gerhart Tepohl, Natalia Corbeto, Marimar Freijo, Christophe Bonny, Joan Martí-Fàbregas, Christopher R Levi, A. Drier, K.M. Kasius, Jens-Rainer Allenberg, Nikolai Steffenhagen, G.J.E. Rinkel, Jessica Fernández-Morales, Joan Montaner, C. van Heugten, Willem P.Th.M. Mali, Bruce Ovbiagele, Imanuel Dzialowski, Dirk Sander, Naomi Morita, S. Deltour, Ryuuji Kaji, Junichiro Satomi, Maite Mendioroz, Georg Bohner, Joaquín Serena, Angelika Alonso, Lorenz Hirt, M. Coudert, Shelagh B. Coutts, Hiromu Nishitani, C.J.M. Frijns, Stephen M. Davis, Jochen B. Fiebach, José Alvarez-Sabín, P. Renou, D. Galanaud, Kotaro Asanuma, Israel Fernandez-Cadenas, Masaaki Uno, Roman L. Haberl, Geoffrey A. Donnan, A. Algra, Soren Christensen, Stefano Ricci, Markus Schwertfeger, Sarah J. Foster, P. Alan Barber, Curt Diehm, Ina Burghaus, Helena Manso, Saskia H. Meves, Patricia Desmond, David Pittrow, Michael G. Hennerici, José M. Ferro, Y. Samson, T. Tourdias, Andrew M. Demchuk, Meng Lee, Victor Obach, Alberto del Rio-Espinola, Frans L. Moll, Lisa M. Jongen, Christine O'Reilly, Shinji Nagahiro, H. Bart van der Worp, João Sobral, Volker Puetz, M.W.M. Post, Bruce C.V. Campbell, Tiago Krug, M.J.E. van Zandvoort, I. Sibon, Stefan H. Kreisel, C. Rosso, J.M.A. Visser-Meily, Harald Darius, Liliana Gouveia, P.E.C.A. Passier, F. Rouanet, Michael D. Hill, Yuishin Izumi, Mark W Parsons, Hans-Joachim Trampisch

Publikováno v: Cerebrovascular Diseases. 29:614-616

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8bb75388434e3a9f6816219c56efe871
https://doi.org/10.1159/000314828

Localisation of the gene for a dominant congenital spinal muscular atrophy predominantly affecting the lower limbs to chromosome 12q23-q24l

Autor: A.J.W. van der Vleuten, C.J.M. Frijns, George W. Padberg, G. Hageman, Arie P. T. Smits, Hannie Kremer, C.M.A. van Ravenswaaij-Arts

Publikováno v: European Journal of Human Genetics, 6, 4, pp. 376-382
European Journal of Human Genetics, 376-382
STARTPAGE=376;ENDPAGE=382;ISSN=1018-4813;TITLE=European Journal of Human Genetics
European Journal of Human Genetics, 6, 376-382
European Journal of Human Genetics, 6, pp. 376-382

Spinal muscular atrophies are a heterogeneous group of disorders. They differ in time of onset, clinical presentation, progression, severity and mode of inheritance. In 1985 a Dutch family was described with a dominant, non-progressive spinal muscula

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d3cb8c9555d0ebe4015e3a387d3f396
https://doi.org/10.1038/sj.ejhg.5200229

Generalized mastocytosis and neurological complications in a 71-year-old patient

Autor: J. Troost, C.J.M. Frijns

Publikováno v: Clinical Neurology and Neurosurgery. 94:257-260

A woman born in 1917 presented with recurrent urticaria since childhood. In the course of her life she developed urticaria pigmentosa, followed by generalized mastocytosis involving the bones, gastro-intestinal tract, and liver. At the age of 71 year

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bd7a927867fc7d6250e70a34192dc9
https://doi.org/10.1016/0303-8467(92)90100-h

Plasminogen activator inhibitor-1 4G allele in the 4G/5G promoter polymorphism increases the occurrence of cerebral ischemia after aneurysmal subarachnoid hemorrhage

Autor: Yvo B.W.E.M. Roos, Frank Baas, C.J.M. Frijns, Mervyn D.I. Vergouwen, G. J. E. Rinkel, Marinus Vermeulen

Publikováno v: Stroke; a journal of cerebral circulation, 35(6), 1280-1283. Lippincott Williams and Wilkins

Background and Purpose— In several acute life-threatening diseases, the 4G-allele in the 4G/5G-promotor polymorphism in the plasminogen activator inhibitor-1 (PAI-1) gene is associated with higher PAI-1 levels and increased poor outcome, probably b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da374328a821527d99540a3c968ab76c
https://pure.amc.nl/en/publications/plasminogen-activator-inhibitor1-4g-allele-in-the-4g5g-promoter-polymorphism-increases-the-occurrence-of-cerebral-ischemia-after-aneurysmal-subarachnoid-hemorrhage(9b503aaa-ef45-46f0-8ebb-a4ee4f1f41a8).html