Neurogenetics

Contributing journals to this collection:
JAMA & Archives Journals

Citations 481-490 of 623 total displayed.

Past content

Basic Science Seminars in Neurology
M-Channels: Neurological Diseases, Neuromodulation, and Drug Development

Edward C. Cooper; Lily Y. Jan
Arch Neurol 2003; 60: 496-500. [Abstract] [Full text] [PDF]  

Special Articles
Screening for Mutations in the MECP2 (Rett Syndrome) Gene in Gilles de la Tourette Syndrome

Alberto L. Rosa; Joseph Jankovic; Tetsuo Ashizawa
Arch Neurol 2003; 60: 502-503. [Extract] [Full text] [PDF]  

Original Contributions
Evidence of Oxidative Stress in Familial Amyloidotic Polyneuropathy Type 1

Mónica L. Fiszman; Marianna Di Egidio; Karina C. Ricart; Marisa G. Repetto; Laura N. Borodinsky; Susana F. Llesuy; Roberto D. Saizar; Pedro L. Trigo; Symon Riedstra; Paulo P. Costa; Andrés M. Villa; Nestor Katz; Javier C. Lendoire; Roberto E. P. Sica
Arch Neurol 2003; 60: 593-597. [Abstract] [Full text] [PDF]  

Observations
Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene

Nazha Birouk; Hamid Azzedine; Odile Dubourg; Marie-Paule Muriel; Ali Benomar; Tarik Hamadouche; Thierry Maisonobe; Reda Ouazzani; Alexis Brice; Mohamed Yahyaoui; Taïb Chkili; Eric Le Guern
Arch Neurol 2003; 60: 598-604. [Abstract] [Full text] [PDF]  

Observations
Transient, Recurrent, White Matter Lesions in X-linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation

C. Oliver Hanemann; Carsten Bergmann; Jan Senderek; Klaus Zerres; Ann-Dorte Sperfeld
Arch Neurol 2003; 60: 605-609. [Abstract] [Full text] [PDF]  

Observations
Phenotypes of Spinocerebellar Ataxia Type 6 and Familial Hemiplegic Migraine Caused by a Unique CACNA1A Missense Mutation in Patients From a Large Family

Isabel Alonso; José Barros; Assunção Tuna; João Coelho; Jorge Sequeiros; Isabel Silveira; Paula Coutinho
Arch Neurol 2003; 60: 610-614. [Abstract] [Full text] [PDF]  

Observations
Dopa-Responsive Dystonia and Tourette Syndrome in a Large Danish Family

Anne Romstad; Erik Dupont; Bente Krag-Olsen; Karen Østergaard; Per Guldberg; Flemming Güttler
Arch Neurol 2003; 60: 618-622. [Abstract] [Full text] [PDF]  

Correspondence
Human Herpesvirus 6 in Serum and Spinal Fluid of Patients With Multiple Sclerosis?—Reply

Roberto Álvarez-Lafuente; Virginia de las Heras; Rafael Arroyo
Arch Neurol 2003; 60: 639-a-640-a. [Extract] [Full text] [PDF]  

Correspondence
Human Herpesvirus 6 in Serum and Spinal Fluid of Patients With Multiple Sclerosis?

Robert Beck; Heinz Wiendl; Gerhard Jahn; Arthur Melms; Frank Neipel
Arch Neurol 2003; 60: 639. [Extract] [Full text] [PDF]  

Neurological Reviews
Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations: A Review

Michaela Auer-Grumbach; Peter De Jonghe; Kristien Verhoeven; Vincent Timmerman; Klaus Wagner; Hans-Peter Hartung; Garth A. Nicholson
Arch Neurol 2003; 60: 329-334. [Abstract] [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