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Genetic Disorders
Citations 281-290 of 396 total displayed.
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Past content
(since Jan 1998):
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- Images in Neurology
Segmental Unilateral Lentiginosis in Generalized Neurofibromatosis Type 1
- Roongroj Bhidayasiri; Stefan-M. Pulst
Arch Neurol 2002; 59: 1331-1332.
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- Original Contributions
Down Syndrome and Alzheimer Disease: Response to Donepezil
- Ira T. Lott; Kathryn Osann; Eric Doran; Linda Nelson
Arch Neurol 2002; 59: 1133-1136.
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- Original Contributions
A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions
- Colette Kananura; Karsten Haug; Thomas Sander; Uwe Runge; Wenli Gu; Kerstin Hallmann; Johannes Rebstock; Armin Heils; Ortrud K. Steinlein
Arch Neurol 2002; 59: 1137-1141.
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- Original Contributions
Interrelationship of Genetics and Prenatal Injury in the Genesis of Malformations of Cortical Development
- Maria Augusta Montenegro; Marilisa M. Guerreiro; Iscia Lopes-Cendes; Carlos A. M. Guerreiro; Fernando Cendes
Arch Neurol 2002; 59: 1147-1153.
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- Original Contributions
The Apolipoprotein E  4 Allele and Decline in Different Cognitive Systems During a 6-Year Period
- Robert S. Wilson; Julie A. Schneider; Lisa L. Barnes; Laurel A. Beckett; Neelum T. Aggarwal; Elizabeth J. Cochran; Elizabeth Berry-Kravis; Julie Bach; Jacob H. Fox; Denis A. Evans; David A. Bennett
Arch Neurol 2002; 59: 1154-1160.
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- Original Contributions
Association Between the Extended tau Haplotype and Frontotemporal Dementia
- Patrice Verpillat; Agnès Camuzat; Didier Hannequin; Catherine Thomas-Anterion; Michèle Puel; Serge Belliard; Bruno Dubois; Mira Didic; Bernard-François Michel; Lucette Lacomblez; Olivier Moreaud; François Sellal; Véronique Golfier; Dominique Campion; Françoise Clerget-Darpoux; Alexis Brice
Arch Neurol 2002; 59: 935-939.
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- Original Contributions
Clinical Features and Disease Haplotypes of Individuals With the N279K tau Gene Mutation: A Comparison of the Pallidopontonigral Degeneration Kindred and a French Family
- Yoshio Tsuboi; Ryan J. Uitti; Marie-Bernadette Delisle; Joaquim J. Ferreira; Christine Brefel-Courbon; Olivier Rascol; Bernardino Ghetti; Jill R. Murrell; Michael Hutton; Matthew Baker; Zbigniew K. Wszolek
Arch Neurol 2002; 59: 943-950.
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- Original Contributions
Molecular Findings in Familial Parkinson Disease in Spain
- Janet Hoenicka; Lídice Vidal; Blas Morales; Israel Ampuero; F. Javier Jiménez-Jiménez; Jose Berciano; Teodoro del Ser; Adriano Jiménez; Pedro G. Ruíz; Justo G. de Yébenes
Arch Neurol 2002; 59: 966-970.
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- Observations
Complex Neurologic Syndrome Associated With the G1606A Mutation of Mitochondrial DNA
- Sabrina Sacconi; Leonardo Salviati; Clifton Gooch; Eduardo Bonilla; Sara Shanske; Salvatore DiMauro
Arch Neurol 2002; 59: 1013-1015.
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- Observations
Mutation Analysis of the CACNA1A Calcium Channel Subunit Gene in 27 Patients With Sporadic Hemiplegic Migraine
- Gisela Terwindt; Esther Kors; Joost Haan; Frans Vermeulen; Arn van den Maagdenberg; Rune Frants; Michel Ferrari; for the International Hemiplegic Migraine Research Group
Arch Neurol 2002; 59: 1016-1018.
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