Результати пошуку - Jurgen Schelhaas
- Показ 1 - 6 результатів із 6
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1
Hereditary spastic paraplegia caused by a mutation in the VCP gene за авторством Susanne T. de Bot, H. Jurgen Schelhaas, Erik‐Jan Kamsteeg, Bart P.C. van de Warrenburg
Опубліковано 2012Carta -
2
Lifetime physical activity and the risk of amyotrophic lateral sclerosis за авторством Mark Huisman, Meinie Seelen, Sonja W. de Jong, Kirsten R.I.S. Dorresteijn, Perry T.C. van Doormaal, Anneke J. van der Kooi, Marianne de Visser, H. Jurgen Schelhaas, Leonard H. van den Berg, Jan H. Veldink
Опубліковано 2013Artigo -
3
A frameshift mutation in LRSAM1 is responsible for a dominant hereditary polyneuropathy за авторством Marian A. J. Weterman, Vincenzo Sorrentino, Paul R. Kasher, Marja E. Jakobs, Baziel G.M. van Engelen, Kees Fluiter, Marit B. de Wissel, Aleksander Sizarov, Gudrun Nürnberg, Peter Nürnberg, Noam Zelcer, H. Jurgen Schelhaas, Frank Baas
Опубліковано 2011Artigo -
4
The ALS-FTD-Q за авторством Joost Raaphorst, Emma Beeldman, Ben Schmand, J. J. Berkhout, Wim H.J.P. Linssen, Leonard H. van den Berg, Yolande A.L. Pijnenburg, Hepke Grupstra, Janneke G. Weikamp, H. Jurgen Schelhaas, Janne M. Papma, John C. van Swieten, Marjolein Visser, Rob J. de Haan
Опубліковано 2012Artigo -
5
Differentiation of Hereditary Spastic Paraparesis From Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron Syndromes за авторством F. Brugman, Jan H. Veldink, Hessel Franssen, Marianne de Visser, J.M.B.V. de Jong, Carin G. Faber, B. Kremer, H. Jurgen Schelhaas, Pieter A. van Doorn, Jan J.G.M. Verschuuren, R.P.M. Bruyn, Jan B. M. Kuks, Wim Robberecht, John H. J. Wokke, Leonard H. van den Berg
Опубліковано 2009Artigo -
6
Lessons learned from 40 novel <i>PIGA</i> patients and a review of the literature за авторством Allan Bayat, Alexej Knaus, Manuela Pendziwiat, Alexandra Afenjar, Tahsin Stefan Barakat, Friedrich Bosch, Bert Callewaert, Patrick Calvas, Berten Ceulemans, Nicolas Chassaing, Christel Depienne, Milda Endzinienė, Carlos R. Ferreira, Carolina Fischinger Moura de Souza, Cécile Freihuber, Shiva Ganesan, Svetlana Gataullina, Renzo Guerrini, Anne‐Marie Guerrot, Lars Hestbjerg Hansen, Aleksandra Jezela‐Stanek, C. Karsenty, Anneke Kievit, R. Frank Kooy, Christian Korff, Johanne Kragh Hansen, Martin J. Larsen, Valérie Layet, Gaëtan Lesca, Kim L. McBride, Marije Meuwissen, Cyril Mignot, Martino Montomoli, Hannah W. Moore, Sophie Naudion, Caroline Nava, Marie‐Christine Nouguès, Elena Parrini, Matthew Pastore, Jurgen Schelhaas, Steven A. Skinner, Krzysztof Szczałuba, Ashley Thomas, Mads Thomassen, Lisbeth Tranebjærg, Marjon van Slegtenhorst, Lynne A. Wolfe, Dennis Lal, Elena Gardella, Lilian Bomme Ousager, Tobias Brünger, Ingo Helbig, Peter Krawitz, Rikke S. Møller
Опубліковано 2020Revisão
Інструменти для пошуку:
Пов'язані теми
Medicine
Psychology
Amyotrophic lateral sclerosis
Biology
Disease
Gene
Genetics
Physical medicine and rehabilitation
Hereditary spastic paraplegia
Mutation
Neuroscience
Pathology
Phenotype
Psychiatry
Spinal cord
Cerebral palsy
Dementia
Exon
Frameshift mutation
Frontotemporal dementia
Internal medicine
Missense mutation
Molecular biology
Motor neuron
Multiple sclerosis
Paraplegia
Physical activity
Psychoanalysis
Sanger sequencing
Spastic