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Neurogenetics
Citations 421-430 of 574 total displayed.
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Past content
(since May 1998):
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- Observations
Presenilin 1 Mutation in an African American Family Presenting With Atypical Alzheimer Dementia
- Gregory A. Rippon; Richard Crook; Matthew Baker; Elizabeth Halvorsen; Steven Chin; Michael Hutton; Henry Houlden; John Hardy; Timothy Lynch
Arch Neurol 2003; 60: 884-888.
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- Images in Neurology
Kennedy Disease: Avoiding Misdiagnosis
- Konstantinos Paparounas; Anna Gotsi; Maria Syrrou; Nikolaos Akritidis
Arch Neurol 2003; 60: 893-894.
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- Basic Science Seminars in Neurology
Application of Microarrays to Neurological Disease
- Lisa-Marie Sturla; Ana Fernandez-Teijeiro; Scott L. Pomeroy
Arch Neurol 2003; 60: 676-682.
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- Original Contributions
Expanding the Phenotypic Spectrum of the CACNA1A Gene T666M Mutation: A Description of 5 Families With Familial Hemiplegic Migraine
- E. E. Kors; J. Haan; N. J. Giffin; L. Pazdera; C. Schnittger; G. G. Lennox; G. M. Terwindt; F. L. M. J. Vermeulen; A. M. J. M. Van den Maagdenberg; R. R. Frants; M. D. Ferrari
Arch Neurol 2003; 60: 684-688.
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- Original Contributions
Novel Tau Polymorphisms, Tau Haplotypes, and Splicing in Familial and Sporadic Frontotemporal Dementia
- Maria-Jesús Sobrido; Bruce L. Miller; Necat Havlioglu; Victoria Zhukareva; Zhihong Jiang; Ziad S. Nasreddine; Virginia M.-Y. Lee; Tiffany W. Chow; Kirk C. Wilhelmsen; Jeffrey L. Cummings; Jane Y. Wu; Daniel H. Geschwind
Arch Neurol 2003; 60: 698-702.
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- Original Contributions
Incipient CADASIL
- Saskia A. J. Lesnik Oberstein; Rivka van den Boom; Huub A. M. Middelkoop; Michel D. Ferrari; Yvette M. Knaap; Hans C. van Houwelingen; Martijn H. Breuning; Mark A. van Buchem; Joost Haan
Arch Neurol 2003; 60: 707-712.
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- Original Contributions
Young-Onset Parkinson Disease With and Without Parkin Gene Mutations: A Fluorodopa F 18 Positron Emission Tomography Study
- Stéphane Thobois; Maria-Joao Ribeiro; Ebba Lohmann; Alexandra Dürr; Pierre Pollak; Olivier Rascol; Stéphane Guillouet; Elizabeth Chapoy; Nicolas Costes; Yves Agid; Philippe Remy; Alexis Brice; Emmanuel Broussolle
Arch Neurol 2003; 60: 713-718.
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- Original Contributions
A Common NURR1 Polymorphism Associated With Parkinson Disease and Diffuse Lewy Body Disease
- Kangni Zheng; Bobak Heydari; David K. Simon
Arch Neurol 2003; 60: 722-725.
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- Original Contributions
Molecular Diagnosis and Prophylactic Therapy for Presymptomatic Chinese Patients With Wilson Disease
- Zhi-Ying Wu; Min-Ting Lin; Shen-Xing Murong; Ning Wang
Arch Neurol 2003; 60: 737-741.
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- Observations
Congenital Myasthenic Syndrome With Episodic Apnea in Patients Homozygous for a CHAT Missense Mutation
- Simone Kraner; Iris Laufenberg; Hans M. Straßburg; Joern P. Sieb; Ortrud K. Steinlein
Arch Neurol 2003; 60: 761-763.
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