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Showing articles 0 to 12 of 12

Filter Applied: Friedreich's ataxia (Click to remove)

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

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

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

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

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

Friedreich's Ataxia:MR Findings Involving the Cervical Portion of the Spinal Cord
AJR 163:187-191, Mascalchi,M.,et al, 1994

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

The Treatment of Friedreich's Ataxia with Amantadine Hydrochloride
Neurol 38:1478-1480, Peterson,P.L.,et al, 1988

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977



Showing articles 0 to 12 of 12