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Mitochondrial disorders

Citations 1-10 of 93 total displayed.

Most recent content (15 Dec 2009):
CLINICAL/SCIENTIFIC NOTES
CHARACTERISTIC BRAIN MRI APPEARANCE OF ERDHEIM-CHESTER DISEASE
F. Bianco, E. Iacovelli, E. Tinelli, N. Locuratolo, F. Pauri, and F. Fattapposta
Neurology 2009; 73: 2120-2122. [Full text] [PDF]  

Past content (since Mar 2001):
RESIDENT AND FELLOW SECTION
Child Neurology: A case illustrating the role of imaging in evaluation of sudden infant death
Sarah M. Kranick, Jaya Ganesh, Curtis R. Coughlin, II, and Daniel J. Licht
Neurology 2009; 73: e54-56e. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
TEMPOROMANDIBULAR SYMPTOMS, MIGRAINE, AND CHRONIC DAILY HEADACHES IN THE POPULATION
D.A.G. Gonçalves, J. G. Speciali, L. C.F. Jales, C. M. Camparis, and M. E. Bigal
Neurology 2009; 73: 645-646. [Full text] [PDF]  

EDITORIALS
Paraoxonase genes and susceptibility to ALS
David A. Greenberg, William C.L. Stewart, and Lewis P. Rowland
Neurology 2009; 73: 11-12. [Full text] [PDF]  

RESIDENT AND FELLOW SECTION
Clinical Reasoning: Blurred vision and dancing feet: Restless legs syndrome presenting in mitochondrial disease
H. Aitken, G. Gorman, R. McFarland, M. Roberts, R. W. Taylor, and D. M. Turnbull
Neurology 2009; 72: e86-90e. [Full text] [PDF]  

ARTICLES
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs
C. Di Lorenzo, F. Pierelli, G. Coppola, G. S. Grieco, C. Rengo, M. Ciccolella, D. Magis, M. Bolla, C. Casali, F. M. Santorelli, and J. Schoenen
Neurology 2009; 72: 1588-1594. [Abstract] [Full text] [PDF]  

RESIDENT AND FELLOW SECTION
Clinical Reasoning: A 62-year-old woman with deafness, unilateral visual loss, and episodes of numbness
Brian C. Callaghan, Sashank Prasad, and Steven L. Galetta
Neurology 2009; 72: e72-78e. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
OCULAR TILT REACTION: A CLINICAL SIGN OF CEREBELLAR INFARCTIONS?
Bernhard Baier and Marianne Dieterich
Neurology 2009; 72: 572-573. [Full text] [PDF]  

ARTICLES
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
R. Del Bo, M. Moggio, M. Rango, S. Bonato, M. G. D’Angelo, S. Ghezzi, G. Airoldi, M. T. Bassi, M. Guglieri, L. Napoli, C. Lamperti, S. Corti, A. Federico, N. Bresolin, and G. P. Comi
Neurology 2008; 71: 1959-1966. [Abstract] [Full text] [PDF]  

ARTICLES
Diagnosing disconjugate eye movements: Phase-plane analysis of horizontal saccades
Alessandro Serra, Ke Liao, Manuela Matta, and R. John Leigh
Neurology 2008; 71: 1167-1175. [Abstract] [Full text] [PDF]  

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* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes

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