Ataxia

Contributing journals to this collection:
JAMA & Archives Journals

Citations 21-30 of 52 total displayed.

Past content

Observations
POLG1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth Disease

Timothy Harrower; Joanna D. Stewart; Gavin Hudson; Henry Houlden; Graham Warner; Dominic G. O’Donovan; Leslie J. Findlay; Robert W. Taylor; Rajith De Silva; Patrick F. Chinnery
Arch Neurol 2008; 65: 133-136. [Abstract] [Full text] [PDF] [ VIDEO SUPPLEMENT ]  

Original Contributions
Chronic Pain in Machado-Joseph Disease: A Frequent and Disabling Symptom

Marcondes C. França Jr; Anelyssa D’Abreu; Joseph H. Friedman; Anamarli Nucci; Iscia Lopes-Cendes
Arch Neurol 2007; 64: 1767-1770. [Abstract] [Full text] [PDF]  

Observations
Mitochondrial Complex I Gene Variant Associated With Early Age at Onset in Spinocerebellar Ataxia Type 2

David K. Simon; Kangni Zheng; Luis Velázquez; Nieves Santos; Luis Almaguer; K. Pattie Figueroa; Stefan-M. Pulst
Arch Neurol 2007; 64: 1042-1044. [Abstract] [Full text] [PDF]  

Clinical Trials
Safety, Tolerability, and Pharmacokinetics of High-Dose Idebenone in Patients With Friedreich Ataxia

Nicholas A. Di Prospero; Charlotte J. Sumner; Scott R. Penzak; Bernard Ravina; Kenneth H. Fischbeck; J. Paul Taylor
Arch Neurol 2007; 64: 803-808. [Abstract] [Full text] [PDF]  

Correspondence
Another Mutation in Cysteine 131 in Protein Kinase C as a Cause of Spinocerebellar Ataxia Type 14

Stephan Klebe; Laurence Faivre; Sylvie Forlani; Christel Dussert; Ayman Tourbah; Alexis Brice; Giovanni Stevanin; Alexandra Durr
Arch Neurol 2007; 64: 913-914. [Extract] [Full text] [PDF]  

Observations
Association of a Presenilin 1 S170F Mutation With a Novel Alzheimer Disease Molecular Phenotype

Alessandra Piccini; Gianluigi Zanusso; Roberta Borghi; Cristiana Noviello; Salvatore Monaco; Roberta Russo; Gianluca Damonte; Andrea Armirotti; Matteo Gelati; Renzo Giordano; Pamela Zambenedetti; Claudio Russo; Bernardino Ghetti; Massimo Tabaton
Arch Neurol 2007; 64: 738-745. [Abstract] [Full text] [PDF]  

Observations
A New Episodic Ataxia Syndrome With Linkage to Chromosome 19q13

Kevin A. Kerber; Joanna C. Jen; Hane Lee; Stanley F. Nelson; Robert W. Baloh
Arch Neurol 2007; 64: 749-752. [Abstract] [Full text] [PDF]  

Original Contributions
Neurological, Cardiological, and Oculomotor Progression in 104 Patients With Friedreich Ataxia During Long-term Follow-up

Pascale Ribaï; Françoise Pousset; Marie-Laure Tanguy; Sophie Rivaud-Pechoux; Isabelle Le Ber; Franchesca Gasparini; Perrine Charles; Anne-Sophie Béraud; Michele Schmitt; Michel Koenig; Alain Mallet; Alexis Brice; Alexandra Dürr
Arch Neurol 2007; 64: 558-564. [Abstract] [Full text] [PDF]  

Correspondence
Fragile X Syndrome vs Fragile X–Associated Tremor/Ataxia Syndrome—Reply

Elena Cellini; Paolo Forleo; Andrea Ginestroni; Benedetta Nacmias; Andrea Tedde; Silvia Bagnoli; Silvia Piacentini; Mario Mascalchi; Sandro Sorbi
Arch Neurol 2007; 64: 289-a-290-a. [Extract] [Full text] [PDF]  

Correspondence
Fragile X Syndrome vs Fragile X–Associated Tremor/Ataxia Syndrome

Maureen A. Leehey; Randi J. Hagerman; Paul J. Hagerman
Arch Neurol 2007; 64: 289. [Extract] [Full text] [PDF]  

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