Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 441-450 of 623 total displayed.

Past content

Original Contributions
Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis

Collette K. Hand; Rebecca S. Devon; Francois Gros-Louis; Daniel Rochefort; Jawad Khoris; Vincent Meininger; Jean-Pierre Bouchard; William Camu; Michael R. Hayden; Guy A. Rouleau
Arch Neurol 2003; 60: 1768-1771. [Abstract] [Full text] [PDF]  

Editorials
Alzheimer Disease Genes: Presenilin 2 Mutation Number 9 and Still Counting

Gerard D. Schellenberg
Arch Neurol 2003; 60: 1521-1522. [Extract] [Full text] [PDF]  

Original Contributions
Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease

Andrea Tedde; Benedetta Nacmias; Monica Ciantelli; Paolo Forleo; Elena Cellini; Silvia Bagnoli; Carolina Piccini; Paolo Caffarra; Enrico Ghidoni; Marco Paganini; Laura Bracco; Sandro Sorbi
Arch Neurol 2003; 60: 1541-1544. [Abstract] [Full text] [PDF]  

Original Contributions
Clinical and Neuroradiological Features of Patients With Spinocerebellar Ataxias From Korean Kindreds

Oh Young Bang; Kyoon Huh; Phil Hyu Lee; Hyon J. Kim
Arch Neurol 2003; 60: 1566-1574. [Abstract] [Full text] [PDF]  

Observations
A Korean Kindred With Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation

Yong-Won Cho; Gholam K. Motamedi; Iris Laufenberg; Sung-Il Sohn; Jeong-Geun Lim; Hyung Lee; Sang-Doe Yi; Ju-Hwa Lee; Dae-Kwang Kim; Richard Reba; William D. Gaillard; William H. Theodore; Ronald P. Lesser; Ortrud K. Steinlein
Arch Neurol 2003; 60: 1625-1632. [Abstract] [Full text] [PDF]  

Original Contributions
Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion

Michael Krasnianski; Katharina Eger; Stephan Neudecker; Sibylle Jakubiczka; Stephan Zierz
Arch Neurol 2003; 60: 1421-1425. [Abstract] [Full text] [PDF]  

Observations
Muscle Glycogenosis and Mitochondrial Hepatopathy in an Infant With Mutations in Both the Myophosphorylase and Deoxyguanosine Kinase Genes

Michelangelo Mancuso; Massimiliano Filosto; Seiichi Tsujino; Costanza Lamperti; Sara Shanske; Michéle Coquet; Claude Desnuelle; Salvatore DiMauro
Arch Neurol 2003; 60: 1445-1447. [Abstract] [Full text] [PDF]  

Observations
A Case of Dementia Parkinsonism Resembling Progressive Supranuclear Palsy Due to Mutation in the Tau Protein Gene

Paola Soliveri; Giacomina Rossi; Daniela Monza; Fabrizio Tagliavini; Sylvie Piacentini; Alberto Albanese; Orso Bugiani; Floriano Girotti
Arch Neurol 2003; 60: 1454-1456. [Abstract] [Full text] [PDF]  

Research Letters
APOE Genotype and Cerebral Blood Flow in Healthy Young Individuals

Nikolaos Scarmeas; Christian G. Habeck; Yaakov Stern; Karen E. Anderson
JAMA 2003; 290: 1581-1582. [Extract] [Full text] [PDF]  

Basic Science Seminars in Neurology
Functional Genomics, Fragile X Syndrome, and RNA Interference

Savitha Kalidas; Dean P. Smith
Arch Neurol 2003; 60: 1197-1200. [Extract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page] Pages: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63