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Genetic Disorders
Citations 61-70 of 396 total displayed.
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Past content
(since Jan 1998):
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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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- Original Contributions
Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene
- Jonathan D. Rohrer; Jason D. Warren; Rohani Omar; Simon Mead; Jonathan Beck; Tamas Revesz; Janice Holton; John M. Stevens; Safa Al-Sarraj; Stuart M. Pickering-Brown; John Hardy; Nick C. Fox; John Collinge; Elizabeth K. Warrington; Martin N. Rossor
Arch Neurol 2008; 65: 506-513.
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- Original Contributions
Patients Homozygous and Heterozygous for SNCA Duplication in a Family With Parkinsonism and Dementia
- Takeshi Ikeuchi; Akiyoshi Kakita; Atsushi Shiga; Kensaku Kasuga; Hiryoyuki Kaneko; Chun-Feng Tan; Jiro Idezuka; Koichi Wakabayashi; Osamu Onodera; Takeshi Iwatsubo; Masatoyo Nishizawa; Hitoshi Takahashi; Atsushi Ishikawa
Arch Neurol 2008; 65: 514-519.
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- Original Contributions
Lack of Spartin Protein in Troyer Syndrome: A Loss-of-Function Disease Mechanism?
- Joanna C. Bakowska; Heng Wang; Baozhong Xin; Charlotte J. Sumner; Craig Blackstone
Arch Neurol 2008; 65: 520-524.
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