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Ataxia
Citations 11-20 of 49 total displayed.
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Past content
(since Jul 1998):
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- Images in Neurology
Progressive Ataxia and Palatal Tremor
- Vesna V. Brinar; Barbara Barun; Ivana Zadro; David Ozretic; Mario Habek
Arch Neurol 2008; 65: 1248-1249.
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- Observations
Clinical and Neuropathologic Findings in a Woman With the FMR1 Premutation and Multiple Sclerosis
- Claudia M. Greco; Flora Tassone; Dolores Garcia-Arocena; Nicole Tartaglia; Sarah M. Coffey; Timothy K. Vartanian; James A. Brunberg; Paul J. Hagerman; Randi J. Hagerman
Arch Neurol 2008; 65: 1114-1116.
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- Original Contributions
Clinical and Molecular Findings of Ataxia With Oculomotor Apraxia Type 2 in 4 Families
- Mathieu Anheim; Marie-Celine Fleury; Jerome Franques; Maria-Ceu Moreira; Jean-Pierre Delaunoy; Dominique Stoppa-Lyonnet; Michel Koenig; Christine Tranchant
Arch Neurol 2008; 65: 958-962.
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- Observations
Large CACNA1A Deletion in a Family With Episodic Ataxia Type 2
- Florence Riant; Reda Mourtada; Pascale Saugier-Veber; Elisabeth Tournier-Lasserve
Arch Neurol 2008; 65: 817-820.
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- Observations
Ocular Flutter, Generalized Myoclonus, and Trunk Ataxia Associated With Anti-GQ1b Antibodies
- Olivier Zaro-Weber; Norbert Galldiks; Christian Dohmen; Gereon R. Fink; Dennis A. Nowak
Arch Neurol 2008; 65: 659-661.
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- Original Contributions
Abnormal Nerve Conduction Features in Fragile X Premutation Carriers
- Kultida Soontarapornchai; Ricardo Maselli; Grace Fenton-Farrell; Flora Tassone; Paul J. Hagerman; Davis Hessl; Randi J. Hagerman
Arch Neurol 2008; 65: 495-498.
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- Original Contributions
Muscle Excitability Abnormalities in Machado-Joseph Disease
- Marcondes C. França Jr; Anelyssa D’Abreu; Anamarli Nucci; Iscia Lopes-Cendes
Arch Neurol 2008; 65: 525-529.
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- Original Contributions
Impaired Eye Movements in Presymptomatic Spinocerebellar Ataxia Type 6
- Peka Christova; John H. Anderson; Christopher M. Gomez
Arch Neurol 2008; 65: 530-536.
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- Neurological Reviews
Fragile X–Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
- Khaled Amiri; Randi J. Hagerman; Paul J. Hagerman
Arch Neurol 2008; 65: 19-25.
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- 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.
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