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neurogenetics

Ausgabe 2/2004

Inhalt (8 Artikel)

Original Article

Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients

Sebastien Couillard-Despres, Goekhan Uyanik, Sonja Ploetz, Claudia Karl, Hartmut Koch, Juergen Winkler, Ludwig Aigner

Original Article

Towards a transcriptome definition of microglial cells

L. B. Moran, D. C. Duke, F. E. Turkheimer, R. B. Banati, M. B. Graeber

Original Article

Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16

Luc Djoussé, Beth Knowlton, Michael R. Hayden, Elisabeth W. Almqvist, Ryan R. Brinkman, Christopher A. Ross, Russel L. Margolis, Adam Rosenblatt, Alexandra Durr, Catherine Dode, Patrick J. Morrison, Andrea Novelletto, Marina Frontali, Ronald J. A. Trent, Elizabeth McCusker, Estrella Gómez-Tortosa, David Mayo Cabrero, Randi Jones, Andrea Zanko, Martha Nance, Ruth K. Abramson, Oksana Suchowersky, Jane S. Paulsen, Madaline B. Harrison, Qiong Yang, L. Adrienne Cupples, Jayalakshmi Mysore, James F. Gusella, Marcy E. MacDonald, Richard H. Myers

Original Article

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease

Mia E.-L. Blomqvist, Peter A. Silburn, Daniel D. Buchanan, Niels Andreasen, Kaj Blennow, Nancy L. Pedersen, Anthony J. Brookes, George D. Mellick, Jonathan A. Prince

Original Article

Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease

Katrina A. B. Goddard, Jane M. Olson, Haydeh Payami, Monique van der Voet, Helena Kuivaniemi, Gerard Tromp

Original Article

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

Natalie J. Colson, Rod A. Lea, Sharon Quinlan, John MacMillan, Lyn R. Griffiths

Original Article

Mutations of the MTHFR gene (428C>T and [458G>T+459C>T]) markedly decrease MTHFR enzyme activity

Hidetaka Yano, Kazuhiro Nakaso, Kenichi Yasui, Yosuke Wakutani, Hiroyuki Nakayasu, Hisanori Kowa, Yoshiki Adachi, Kenji Nakashima

Short Communication

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

M. A. Kaunisto, H. Harno, K. R. J. Vanmolkot, J. J. Gargus, G. Sun, E. Hämäläinen, E. Liukkonen, M. Kallela, A. M. J. M. van den Maagdenberg, R. R. Frants, M. Färkkilä, A. Palotie, M. Wessman

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