Ausgabe 1/2008
Inhalt (10 Artikel)
Towards a pathway definition of Parkinson’s disease: a complex disorder with links to cancer, diabetes and inflammation
Linda B. Moran, Manuel B. Graeber
Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseases
Katrin Beyer, Montserrat Domingo-Sábat, José I. Lao, Cristina Carrato, Isidro Ferrer, Aurelio Ariza
Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts
Christina L. Liquori, Silvana Penco, Judith Gault, Tracey P. Leedom, Laura Tassi, Teresa Esposito, Issam A. Awad, Luigi Frati, Eric W. Johnson, Ferdinando Squitieri, Douglas A. Marchuk, Fernando Gianfrancesco
Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis
Cinzia Gellera, Claudia Colombrita, Nicola Ticozzi, Barbara Castellotti, Cinzia Bragato, Antonia Ratti, Franco Taroni, Vincenzo Silani
A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2
Xuhua Chen, Gary S. Johnson, Robert D. Schnabel, Jeremy F. Taylor, Gayle C. Johnson, Heidi G. Parker, Edward E. Patterson, Martin L. Katz, Tomoyuki Awano, Shahwanaz Khan, Dennis P. O’Brien
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer’s disease
Joseph H. Lee, Sandra Barral, Rong Cheng, Inara Chacon, Vincent Santana, Jennifer Williamson, Rafael Lantigua, Martin Medrano, Ivonne Z. Jimenez-Velazquez, Yaakov Stern, Benjamin Tycko, Ekaterina Rogaeva, Yosuke Wakutani, Toshitaka Kawarai, Peter St George-Hyslop, Richard Mayeux
Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families
Tsukasa Saito, Yoshinobu Amakusa, Takashi Kimura, Osamu Yahara, Hitoshi Aizawa, Yoshio Ikeda, John W. Day, Laura P. W. Ranum, Kinji Ohno, Tohru Matsuura
Familial cases presenting very early onset autosomal dominant Alzheimer’s disease with I143T in presenilin-1 gene: implication for genotype–phenotype correlation
Noritoshi Arai, Atsushi Kishino, Yuji Takahashi, Daiji Morita, Koichiro Nakamura, Takahiro Yokoyama, Tomoji Watanabe, Masayoshi Ida, Jun Goto, Shoji Tsuji
Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genes
Cécile Saint-Martin, Delphine Bouteiller, Giovanni Stevanin, Cyprian Popescu, Céline Charon, Merle Ruberg, Stéphanie Baulac, Eric LeGuern, Pierre Labauge, Christel Depienne
Genetic susceptibility to Parkinson’s disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker
Ramesh C. Juyal, Mitashree Das, Sohan Punia, Madhuri Behari, Geetika Nainwal, Sumit Singh, Pazhayannur V. Swaminath, Shyla T. Govindappa, Sachi Jayaram, Uday B. Muthane, B. K. Thelma