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Genetic Disorders
Citations 331-340 of 396 total displayed.
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Past content
(since Jan 1998):
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- Observations
A Family With X-linked Dystonia-Deafness Syndrome With a Novel Mutation of the DDP Gene
- Hiroshi Ujike; Yasuyuki Tanabe; Yasushi Takehisa; Toshiyuki Hayabara; Shigetoshi Kuroda
Arch Neurol 2001; 58: 1004-1007.
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- History of Neurology: Seminal Citations
Charcot-Marie-Tooth Disease
- A. Gordon Smith
Arch Neurol 2001; 58: 1014-1016.
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- Original Contributions
Familial Amyotrophic Lateral Sclerosis With a Novel Leu126Ser Mutation in the Copper/Zinc Superoxide Dismutase Gene Showing Mild Clinical Features and Lewy Body–Like Hyaline Inclusions
- Yasushi Takehisa; Hiroshi Ujike; Hideki Ishizu; Seishi Terada; Takashi Haraguchi; Yuji Tanaka; Tetsuya Nishinaka; Keigo Nobukuni; Yuetsu Ihara; Reiko Namba; Takeshi Yasuda; Masahiro Nishibori; Toshiyuki Hayabara; Shigetoshi Kuroda
Arch Neurol 2001; 58: 736-740.
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- Original Contributions
Neurologic and Psychiatric Manifestations in a Family With a Mutation in Exon 2 of the Guanosine Triphosphate–Cyclohydrolase Gene
- Heidi Hahn; Melissa R. Trant; Michael J. Brownstein; R. Andrew Harper; Sheldon Milstien; Ian J. Butler
Arch Neurol 2001; 58: 749-755.
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- Original Contributions
Cerebrovascular and Brain Morphologic Correlates of Mild Cognitive Impairment in the National Heart, Lung, and Blood Institute Twin Study
- Charles DeCarli; Bruce L. Miller; Gary E. Swan; Terry Reed; Philip A. Wolf; Dorit Carmelli
Arch Neurol 2001; 58: 643-647.
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- Original Contributions
Genetic Variation Analysis in Parkinson Disease Patients With and Without Hallucinations: Case-Control Study
- Christopher G. Goetz; Paul F. Burke; Sue Leurgans; Elizabeth Berry-Kravis; Lucy M. Blasucci; Rema Raman; Lili Zhou
Arch Neurol 2001; 58: 209-213.
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- Original Contributions
Progression of Symptoms in the Early and Middle Stages of Huntington Disease
- Sandra Close Kirkwood; Jessica L. Su; P. Michael Conneally; Tatiana Foroud
Arch Neurol 2001; 58: 273-278.
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- Observations
Missense CACNA1A Mutation Causing Episodic Ataxia Type 2
- Christian Denier; Anne Ducros; Alexandra Durr; Bruno Eymard; Bénédicte Chassande; Elisabeth Tournier-Lasserve
Arch Neurol 2001; 58: 292-295.
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- Observations
Spinocerebellar Ataxia Type 3 Phenotypically Resembling Parkinson Disease in a Black Family
- Katrina Gwinn-Hardy; Andrew Singleton; Padraig O'Suilleabhain; Michael Boss; David Nicholl; Amanda Adam; Jennifer Hussey; P. Critchley; John Hardy; Matthew Farrer
Arch Neurol 2001; 58: 296-299.
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- History of Neurology: Seminal Citations
Huntington Disease
- Eric Siemers
Arch Neurol 2001; 58: 308-310.
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