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EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders.
Published in:
European Journal of Neurology, 2011, v. 18, n. 2, p. 207, doi. 10.1111/j.1468-1331.2010.03069.x
By:
- Burgunder, J.-M.;
- Schöls, L.;
- Baets, J.;
- Andersen, P.;
- Gasser, T.;
- Szolnoki, Z.;
- Fontaine, B.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- De Jonghe, P.;
- Lynch, T.;
- Mariotti, C.;
- Spinazzola, A.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Harbo, H. F.;
- Finsterer, J.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
Published in:
European Journal of Neurology, 2010, v. 17, n. 5, p. 641, doi. 10.1111/j.1468-1331.2010.02985.x
By:
- Burgunder, J.-M.;
- Finsterer, J.;
- Szolnoki, Z.;
- Fontaine, B.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- De Jonghe, P.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Harbo, H. F.;
- Gasser, T.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.
Published in:
European Journal of Neurology, 2010, v. 17, n. 2, p. 179, doi. 10.1111/j.1468-1331.2009.02873.x
By:
- Gasser, T.;
- Finsterer, J.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C. M. E.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Harbo, H. F.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of mitochondrial disorders.
Published in:
European Journal of Neurology, 2009, v. 16, n. 12, p. 1255, doi. 10.1111/j.1468-1331.2009.02811.x
By:
- Finsterer, J.;
- Harbo, H. F.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C. M. E.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Gasser, T.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington’s disease, Parkinson’s disease and dystonias.
Published in:
European Journal of Neurology, 2009, v. 16, n. 7, p. 777, doi. 10.1111/j.1468-1331.2009.02646.x
By:
- Harbo, H. F.;
- Finsterer, J.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Gasser, T.
Publication type:
Article
Service quality for Type 2 diabetes in Australia: the patient perspective.
Published in:
Diabetic Medicine, 2008, v. 25, n. 5, p. 612, doi. 10.1111/j.1464-5491.2008.02420.x
By:
- Tabrizi, J. S.;
- O’Rourke, P. K.;
- Wilson, A. J.;
- Coyne, E. T.
Publication type:
Article
A Huntington's disease phenocopy characterized by pallido-nigro-luysian degeneration with brain iron accumulation and p62-positive glial inclusions.
Published in:
2010
By:
- Ahmed, Z.;
- Tabrizi, S. J.;
- Li, A.;
- Houlden, H.;
- Sailer, A.;
- Lees, A. J.;
- Revesz, T.;
- Holton, J. L.
Publication type:
Other
Proteome-based plasma biomarkers for Alzheimer's disease.
Published in:
Brain: A Journal of Neurology, 2006, v. 129, n. 11, p. 3042, doi. 10.1093/brain/awl279
By:
- A. Hye;
- S. Lynham;
- M. Thambisetty;
- M. Causevic;
- J. Campbell;
- H. L. Byers;
- C. Hooper;
- F. Rijsdijk;
- S. J. Tabrizi;
- S. Banner;
- C. E. Shaw;
- C. Foy;
- M. Poppe;
- N. Archer;
- G. Hamilton;
- J. Powell;
- R. G. Brown;
- P. Sham;
- M. Ward;
- S. Lovestone
Publication type:
Article
Investigating the effect of Interventions on improving the Service Quality of Physiotherapy Clinic in Rehabilitation Faculty of Tabriz in 2011-2012.
Published in:
Journal of Fasa University of Medical Sciences, 2014, v. 3, n. 4, p. 348
By:
- Tabrizi, J. S.;
- Gharibi, F.;
- Eteraf Oskouei, M. A.;
- Asghari Jafarabadi, M.
Publication type:
Article
Ethical issues in human prion diseases.
Published in:
British Medical Bulletin, 2003, v. 66, n. 1, p. 305, doi. 10.1093/bmb/66.1.305
By:
- S J Tabrizi;
- C L Elliott;
- C Weissmann
Publication type:
Article
Huntington's disease: a clinical review.
Published in:
European Journal of Neurology, 2018, v. 25, n. 1, p. 24, doi. 10.1111/ene.13413
By:
- McColgan, P.;
- Tabrizi, S. J.
Publication type:
Article
Iranian public trust in health services: evidence from Tabriz, Islamic Republic of Iran.
Published in:
Eastern Mediterranean Health Journal, 2016, v. 22, n. 10, p. 713, doi. 10.26719/2016.22.10.713
By:
- Tabrizi, J. S.;
- Saadati, M.;
- Sadeghi-Bazargani, H.;
- Abedi, L.;
- Alibabayee, R.
Publication type:
Article
Customer's self-audit to improve the technical quality of maternity care in Tabriz: a community trial.
Published in:
Eastern Mediterranean Health Journal, 2016, v. 22, n. 5, p. 309, doi. 10.26719/2016.22.5.309
By:
- Gholipour, K.;
- Tabrizi, J. S.;
- Asghari-Jafarabadi, M.;
- Iezadi, S.;
- Farshbaf, N.;
- Rahbar-Farzam, F.;
- Afsharniya, F.
Publication type:
Article
Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse.
Published in:
2000
By:
- Tabrizi SJ;
- Workman J;
- Hart PE;
- Mangiarini L;
- Mahal A;
- Bates G;
- Cooper JM;
- Schapira AHV;
- Tabrizi, S J;
- Workman, J;
- Hart, P E;
- Mangiarini, L;
- Mahal, A;
- Bates, G;
- Cooper, J M;
- Schapira, A H
Publication type:
journal article
Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse.
Published in:
Annals of Neurology, 2000, v. 47, n. 1, p. 80, doi. 10.1002/1531-8249(200001)47:1<80::AID-ANA13>3.0.CO;2-K
By:
- Tabrizi, S. J.;
- Workman, J.;
- Hart, P. E.;
- Mangiarini, L.;
- Mahal, A.;
- Bates, G.;
- Cooper, J. M.;
- Schapira, A. H. V.
Publication type:
Article
Biochemical abnormalities and excitotoxicity in Huntington's disease brain.
Published in:
1999
By:
- Tabrizi, S. J.;
- Cleeter, M. W. J.;
- Xuereb, J.;
- Taanman, J.-W.;
- Cooper, J. M.;
- Schapira, A. H. V.;
- Cleeter, M W;
- Schapira, A H
Publication type:
journal article
Mitochondria in the etiology and pathogenesis of Parkinson's disease.
Published in:
1998
By:
- Schapira, A. H. V.;
- Gu, M.;
- Taanman, J.-W.;
- Tabrizi, S. J.;
- Seaton, T.;
- Cleeter, M.;
- Cooper, J. M.;
- Schapira, A H
Publication type:
journal article
The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy.
Published in:
Annals of Neurology, 1998, v. 44, n. 2, p. 187, doi. 10.1002/ana.410440208
By:
- Cock, H. R.;
- Tabrizi, S. J.;
- Cooper, J. M.;
- Schapira, A. H. V.
Publication type:
Article
Mitochondrial DNA in focal dystonia: A cybrid analysis.
Published in:
Annals of Neurology, 1998, v. 44, n. 2, p. 258, doi. 10.1002/ana.410440218
By:
- Tabrizi, S. J.;
- Cooper, J. M.;
- Schapira, A. H. V.
Publication type:
Article
In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by <sup>31</sup>P magnetic resonance spectroscopy.
Published in:
Annals of Neurology, 1997, v. 42, n. 4, p. 573, doi. 10.1002/ana.410420407
By:
- Lodi, R.;
- Taylor, D. J.;
- Tabrizi, S. J.;
- Kumar, S.;
- Sweeney, M.;
- Wood, N. W.;
- Styles, P.;
- Radda, G. K.;
- Schapira, A. H. V.
Publication type:
Article

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