A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023
Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017
Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014
The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012
Neurological,Cardiological,and Oculomotor Progression in 104 Patients with Freidreich Ataxia During Long-Term Follow-Up
Arch Neurol 64:558-564, Rabai,P.,et al, 2007
Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005
Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002
Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001
Cardiac Dysfunction in Neuromuscular Diseases
The Neurologist 6:67-82, Pourmand,R., 2000
Very Late-Onset Friedreich Ataxia Despite Large GAA Triplet Repeat Expansions
Arch Neurol 57:246-251, Bidichandani,S.I.,et al, 2000
Increased Levels of Plasma Malondialdehyde in Friedreich Ataxia
Neurol 55:1752-1753,1600, Emond,M.,et al, 2000
Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999
Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998
Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997
Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997
Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997
Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997
The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996
Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996
Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996
Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995
Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995
Structural and Functional Brain Imaging in Friedreich's Ataxia
Arch Neurol 51:349-355, Junck,L.,et al, 1994
Friedreich's Ataxia:MR Findings Involving the Cervical Portion of the Spinal Cord
AJR 163:187-191, Mascalchi,M.,et al, 1994
The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993
Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993
Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993
Cerebral Glucose Hypermetabolism in Friedreich's Ataxia Detected with Positron Emission Tomography
Ann Neurol 28:750-757, Gilman,S.,et al, 1990
Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989
The Treatment of Friedreich's Ataxia with Amantadine Hydrochloride
Neurol 38:1478-1480, Peterson,P.L.,et al, 1988
Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987
The Heart in Friedreich's Ataxia
Arch Neurol 43:189-192, Brumback,R.A.,et al, 1986
Eye Movements in Friedreich's Ataxia
Arch Neurol 40:343-346, Furman,J.M.,et al, 1983
Lecithin Treatment in Friedreich's Ataxia
BMJ 282:1197-1198, Pentland,B.,et al, 1981
Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981
Jaw Reflex in Friedreich Ataxia
Neurol 29:1049-1050, Salisachs,P., 1979
Lecithin in Neurologic Disorders
NEJM 299:200, 1978 (Letter) ., Barbeau,A., 1978
Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977
Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
NEJM 295:62, Blass,J.P.,et al, 1976
Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972
A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960
Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850
Hereditary Ataxias
Genetics & the Inheritance of Integrated Neurol & Psych. Patterns-Vol 33, Proceed. Assoc. for Resear, h in NerSchut, J., 1850
A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025
A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025
Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025
Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025
A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025
A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025