Neurogenetics

Citations 261-270 of 574 total displayed.

Past content (since May 1998):

Correspondence
Analysis of the LRRK2 G2019S Mutation in Alzheimer Disease

Cyrus P. Zabetian; Chris J. Lauricella; Debby W. Tsuang; James B. Leverenz; Gerard D. Schellenberg; Haydeh Payami
Arch Neurol 2006; 63: 156-157. [Extract] [Full text] [PDF]  

Editorials
New Presenilin 1 Mutation With Alzheimer Disease and Lewy Bodies

Roger N. Rosenberg
Arch Neurol 2005; 62: 1808. [Extract] [Full text] [PDF]  

Neurological Reviews
Therapeutic Potential of Small Interfering RNA for Central Nervous System Diseases

Amy E. Lovett-Racke; Petra D. Cravens; Anne R. Gocke; Michael K. Racke; Olaf Stüve
Arch Neurol 2005; 62: 1810-1813. [Extract] [Full text] [PDF]  

Original Contributions
Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life

B. Joy Snider; Joanne Norton; Mary A. Coats; Sumi Chakraverty; Craig E. Hou; Ramiro Jervis; Corinne L. Lendon; Alison M. Goate; Daniel W. McKeel Jr; John C. Morris
Arch Neurol 2005; 62: 1821-1830. [Abstract] [Full text] [PDF]  

Original Contributions
Late-Onset Friedreich Ataxia: Phenotypic Analysis, Magnetic Resonance Imaging Findings, and Review of the Literature

Roongroj Bhidayasiri; Susan L. Perlman; Stefan-M. Pulst; Daniel H. Geschwind
Arch Neurol 2005; 62: 1865-1869. [Abstract] [Full text] [PDF]  

Original Contributions
Clinical and Molecular Characterization of Patients With Limb-Girdle Muscular Dystrophy Type 2I

Chiara A. Boito; Paola Melacini; Andrea Vianello; Paola Prandini; Bruno F. Gavassini; Alessia Bagattin; Gabriele Siciliano; Corrado Angelini; Elena Pegoraro
Arch Neurol 2005; 62: 1894-1899. [Abstract] [Full text] [PDF]  

Observations
Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies: Description of a Large Family With This Association

Jordi Sanahuja; Elena Franco; Ricardo Rojas-García; Eduard Gallardo; Onofre Combarros; Robert Begué; Pilar Granés; Isabel Illa
Arch Neurol 2005; 62: 1911-1914. [Abstract] [Full text] [PDF]  

Observations
Clinical and Molecular Features of Encephalomyopathy Due to the A3302G Mutation in the Mitochondrial tRNA^Leu(UUR) Gene

Wendy M. Hutchison; Dominic Thyagarajan; Joanna Poulton; David R. Marchington; Denise M. Kirby; Shehnaaz S. M. Manji; Hans-Henrik M. Dahl
Arch Neurol 2005; 62: 1920-1923. [Abstract] [Full text] [PDF]  

Hypothesis
Sturge-Weber Syndrome Associated With Other Abnormalities: A Medical Record and Literature Review

Anne M. Comi; Paulomi Mehta; Laura A. Hatfield; Michael M. Dowling
Arch Neurol 2005; 62: 1924-1927. [Abstract] [Full text] [PDF]  

Neurological Reviews
Microarrays: Applications and Pitfalls

Hassan M. Fathallah-Shaykh
Arch Neurol 2005; 62: 1669-1672. [Abstract] [Full text] [PDF]  

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