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Genetics
Contributing journals to this collection:
BMJ,
,
Molecular Pathology,
Journal of Clinical Pathology,
British Journal of Ophthalmology,
Tobacco Control,
Postgraduate Medical Journal,
Injury Prevention,
Practical Neurology,
Heart,
BMJ Case Reports,
Annals of the Rheumatic Diseases,
Drug and Therapeutics Bulletin,
Evidence-Based Medicine,
Journal of Epidemiology and Community Health,
Journal of Neurology, Neurosurgery, and Psychiatry,
Journal of Medical Genetics,
Journal of NeuroInterventional Surgery,
Journal of Medical Ethics,
Quality and Safety in Health Care,
Emergency Medicine Journal,
Evidence-Based Mental Health,
EULAR Meeting Abstracts,
Gut,
Medical Humanities,
Thorax,
Occupational and Environmental Medicine,
Heart Asia,
Evidence-Based Nursing,
British Journal of Sports Medicine,
and Sexually Transmitted Infections
Citations 1-10 of 1204 total displayed.
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Review
Diagnosis and new treatments in genetic neuropathies
- M M Reilly and M E Shy
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1304-1314.
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Short reports
Inherited Creutzfeldt–Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology
- C Jansen, J C van Swieten, S Capellari, R Strammiello, P Parchi, and A J M Rozemuller
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1386-1389.
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Short reports
Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations
- G Solé, I Coupry, C Rooryck, E Guérineau, F Martins, S Devés, C Hubert, N Souakri, O Boute, C Marchal, L Faivre, E Landré, S Debruxelles, A Dieux-Coeslier, C Boulay, S Chassagnon, V Michel, M-C Routon, A Toutain, N Philip, D Lacombe, L Villard, B Arveiler, and C Goizet
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1394-1398.
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Short reports
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
- R Schüle, N Schlipf, M Synofzik, S Klebe, S Klimpe, U Hehr, B Winner, T Lindig, A Dotzer, O Rieß, J Winkler, L Schöls, and P Bauer
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1402-1404.
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Short reports
Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients
- H Bourteel, P Vermersch, J-M Cuisset, C-A Maurage, P Laforet, P Richard, and T Stojkovic
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1405-1408.
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Basic and translational research
Association of the DVWA and GDF5 polymorphisms with osteoarthritis in UK populations
- A M Valdes, T D Spector, S Doherty, M Wheeler, D J Hart, and M Doherty
Ann Rheum Dis 2009 68: 1916 -1920; published online before print as 10.1136/ard.2008.102236
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Basic and translational research
Association study of a polymorphism of the CTGF gene and susceptibility to systemic sclerosis in the Japanese population
- Y Kawaguchi, Y Ota, M Kawamoto, I Ito, N Tsuchiya, T Sugiura, Y Katsumata, M Soejima, S Sato, M Hasegawa, M Fujimoto, K Takehara, M Kuwana, H Yamanaka, and M Hara
Ann Rheum Dis 2009 68: 1921 -1924; published online before print as 10.1136/ard.2008.100586
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Basic and translational research
Definition of arthritis candidate risk genes by combining rat linkage-mapping results with human case-control association data
- L Bäckdahl, J P Guo, M Jagodic, K Becanovic, B Ding, T Olsson, and J C Lorentzen
Ann Rheum Dis 2009 68: 1925 -1932; published online before print as 10.1136/ard.2008.090803
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Research papers
Screen for intracranial dural arteriovenous fistulae with carotid duplex sonography
- L-K Tsai, S-J Yeh, Y-C Chen, H-M Liu, and J-S Jeng
J. Neurol. Neurosurg. Psychiatry 2009 80: 1225 -1229; published online before print as 10.1136/jnnp.2008.166413
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Neurological pictures
Pagets disease
- F Andrade
J. Neurol. Neurosurg. Psychiatry 2009; 80: 1240.
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