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All Genetics
Citations 451-460 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Characteristics of intracranial aneurysms in patients with familial subarachnoid hemorrhage
- Y.M. Ruigrok, G.J.E. Rinkel, A. Algra, T.W.M. Raaymakers, and J. van Gijn
Neurology 2004; 62: 891-894.
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- BRIEF COMMUNICATIONS
SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I
- K. Verhoeven, K. Coen, E. De Vriendt, A. Jacobs, V. Van Gerwen, I. Smouts, A. Pou–Serradell, J. -J. Martin, V. Timmerman, and P. De Jonghe
Neurology 2004; 62: 1001-1002.
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- BRIEF COMMUNICATIONS
Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation
- Karin Jurkat-Rott and Frank Lehmann-Horn
Neurology 2004; 62: 1012-1015.
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- CLINICAL/SCIENTIFIC NOTES
Familial occurrence of dysembryoplastic neuroepithelial tumor
- M. Hasselblatt, G. Kurlemann, C. H. Rickert, O. M. Debus, A. Brentrup, W. Schachenmayr, and W. Paulus
Neurology 2004; 62: 1020-1021.
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- CLINICAL/SCIENTIFIC NOTES
Focal dystonia caused by Mohr–Tranebjaerg syndrome with complete deletion of the DDP1 gene
- A. Pizzuti, G. Fabbrini, L. Salehi, L. Vacca, M. Inghilleri, B. Dallapiccola, and A. Berardelli
Neurology 2004; 62: 1021-1022.
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- BRIEF COMMUNICATIONS
Monozygotic twins with tuberous sclerosis discordant for the severity of developmental deficits
- Ayla Humphrey, J. Nicholas P. Higgins, John R.W. Yates, and Patrick F. Bolton
Neurology 2004; 62: 795-798.
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- BRIEF COMMUNICATIONS
Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia
- F. R. Torres, M. A. Montenegro, A. P. Marques-de-Faria, M. M. Guerreiro, F. Cendes, and I. Lopes-Cendes
Neurology 2004; 62: 799-802.
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- BRIEF COMMUNICATIONS
TNF-376A marks susceptibility to MS in the Spanish population: A replication study
- A. Martínez, A. Rubio, E. Urcelay, M. Fernández-Arquero, V. de las Heras, R. Arroyo, P. Villoslada, X. Montalbán, and E.G. de la Concha
Neurology 2004; 62: 809-810.
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- BRIEF COMMUNICATIONS
Bilineal transmission of Parkinson disease on Crete suggests a complex inheritance
- Cleanthe Spanaki and Andreas Plaitakis
Neurology 2004; 62: 815-817.
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- VIEWS & REVIEWS
Caveolinopathies: Mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases
- S. E. Woodman, F. Sotgia, F. Galbiati, C. Minetti, and M. P. Lisanti
Neurology 2004; 62: 538-543.
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