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Genetic Disorders
Contributing journals to this collection:
JAMA & Archives Journals
Citations 301-310 of 1368 total displayed.
- Original Articles
A Longitudinal Twin Study of Fears From Middle Childhood to Early Adulthood: Evidence for a Developmentally Dynamic Genome
- Kenneth S. Kendler; Charles O. Gardner; Peter Annas; Michael C. Neale; Lindon J. Eaves; Paul Lichtenstein
Arch Gen Psychiatry 2008; 65: 421-429.
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- Editorials
How to Predict the Risk of Parkinson Disease in Relatives of Parkin Mutation Carriers: A Complex Puzzle of Age, Penetrance, and Number of Mutated Alleles
- Christine Klein; Andreas Ziegler
Arch Neurol 2008; 65: 443-444.
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- Neurological Reviews
The Changing Face of Neural Stem Cell Therapy in Neurologic Diseases
- Ofira Einstein; Tamir Ben-Hur
Arch Neurol 2008; 65: 452-456.
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- Neurological Reviews
Refining Frontotemporal Dementia With Parkinsonism Linked to Chromosome 17: Introducing FTDP-17 (MAPT) and FTDP-17 (PGRN)
- Bradley F. Boeve; Mike Hutton
Arch Neurol 2008; 65: 460-464.
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- Original Contributions
Risk of Parkinson Disease in Carriers of Parkin Mutations: Estimation Using the Kin-Cohort Method
- Yuanjia Wang; Lorraine N. Clark; Elan D. Louis; Helen Mejia-Santana; Juliette Harris; Lucien J. Cote; Cheryl Waters; Howard Andrews; Blair Ford; Steven Frucht; Stanley Fahn; Ruth Ottman; Daniel Rabinowitz; Karen Marder
Arch Neurol 2008; 65: 467-474.
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- Original Contributions
Glucose Homeostasis in Huntington Disease: Abnormalities in Insulin Sensitivity and Early-Phase Insulin Secretion
- Nebojsa M. Lalic; Jelena Maric; Marina Svetel; Aleksandra Jotic; Elka Stefanova; Katarina Lalic; Natasa Dragasevic; Tanja Milicic; Ljiljana Lukic; Vladimir S. Kostic
Arch Neurol 2008; 65: 476-480.
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- Original Contributions
Rapid Eye Movement Sleep Disturbances in Huntington Disease
- Isabelle Arnulf; Jørgen Nielsen; Ebba Lohmann; Johannes Schieffer; Edward Wild; Poul Jennum; Eric Konofal; Matthew Walker; Delphine Oudiette; Sarah Tabrizi; Alexandra Durr
Arch Neurol 2008; 65: 482-488.
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- Original Contributions
Cryptogenic Epileptic Syndromes Related to SCN1A: Twelve Novel Mutations Identified
- Claudio Zucca; Francesca Redaelli; Roberta Epifanio; Nicoletta Zanotta; Antonino Romeo; Monica Lodi; Pierangelo Veggiotti; Giovanni Airoldi; Chris Panzeri; Romina Romaniello; Gianni De Polo; Paolo Bonanni; Simonetta Cardinali; Cinzia Baschirotto; Loreto Martorell; Renato Borgatti; Nereo Bresolin; Maria Teresa Bassi
Arch Neurol 2008; 65: 489-494.
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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
Clinical and Neuropathological Features of the Arctic APP Gene Mutation Causing Early-Onset Alzheimer Disease
- Hans Basun; Nenad Bogdanovic; Martin Ingelsson; Ove Almkvist; Jan Näslund; Karin Axelman; Thomas D. Bird; David Nochlin; Gerard D. Schellenberg; Lars-Olof Wahlund; Lars Lannfelt
Arch Neurol 2008; 65: 499-505.
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