Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene von JAMES, P. A, CADER, M. Z, MUNTONI, F, CHILDS, A.-M, CROW, Y. J, TALBOT, K

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A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia von CADER, M. Z, STECKLEY, J. L, DYMENT, D. A, MCLACHLAN, R. S, EBERS, G. C

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An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus von STECKLEY, J. L, EBERS, G. C, CADER, M. Z, MCLACHLAN, R. S

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Multiple sclerosis susceptibility and the X chromosome von Herrera, BM, Cader, MZ, Dyment, DA, Bell, JT, DeLuca, GC, Willer, CJ, Lincoln, MR, Ramagopalan, SV, Chao, M., Orton, S-M., Sadovnick, AD, Ebers, GC

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A genome scan in a single pedigree with a high prevalence of multiple sclerosis von Dyment, D A, Cader, M Z, Herrera, B M, Ramagopalan, S V, Orton, S M, Chao, M, Willer, C J, Sadovnick, A D, Risch, N, Ebers, G C

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Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13 von NOBLE-TOPHAM, S. E, DYMENT, D. A, CADER, M. Z, GANAPATHY, R, BROWN, J. D, RICE, G. P. A, EBERS, G. C

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The role of hereditary spastic paraplegia related genes in multiple sclerosis : A study of disease susceptibility and clinical outcome von DELUCA, G. C, RAMAGOPALAN, S. V, EBERS, G. C, CADER, M. Z, DYMENT, D. A, HERRERA, B. M, ORTON, S, DEGENHARDT, A, PUGLIATTI, M, SADOVNICK, A. D, SOTGIU, S

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Helicobacter pylori induces human dendritic cell maturation and duodenal ulcer promoting gene a (dupA) enhances dendritic cell cytokine expression von Cader, M Z, Marx, C, Staples, E, Robinson, K, Atherton, J

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Lesson of the Week: Cavernous Haemangioma Mimicking Multiple Sclerosis von Cader, M. Zameel, Winer, J. B.

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A multigenerational family with multiple sclerosis von Dyment, D. A., Cader, M. Z., Willer, C. J., Risch, N., Sadovnick, A. D., Ebers, G. C.

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Genetic loading in familial migraine with aura von Noble-Topham, S E, Cader, M Z, Dyment, D A, Rice, G P A, Brown, J D, Ebers, G C

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Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot–Marie–Tooth type 2D mice von Sleigh, James N., Grice, Stuart J., Burgess, Robert W., Talbot, Kevin, Cader, M. Zameel

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RARE VARIANTS IN THE CYP27B1 GENE ARE ASSOCIATED WITH MULTIPLE SCLEROSIS von Ebers, G, Ramagopalan, SV, Dyment, DA, Cader, ZM, Disanto, G, Handel, A, DeLuca, GC, Sadovnick, AD, Lepage, P, Montpetit, A

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Significant linkage to migraine with aura on chromosome 11q24 von Cader, Zameel M., Noble-Topham, Sandra, Dyment, David A., Cherny, Stacey S., Brown, John D., Rice, George P.A., Ebers, George C.

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Molecular mechanisms of migraine? von RAMAGOPALAN, Sreeram V, RAMSCAR, Nicholas E, ZAMEEL CADER, M

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A disease-associated gene desert directs macrophage inflammation through ETS2 von Stankey, C. T., Bourges, C., Haag, L. M., Turner-Stokes, T., Piedade, A. P., Palmer-Jones, C., Papa, I., Silva dos Santos, M., Zhang, Q., Cameron, A. J., Legrini, A., Zhang, T., Wood, C. S., New, F. N., Randzavola, L. O., Speidel, L., Brown, A. C., Hall, A., Saffioti, F., Parkes, E. C., Edwards, W., Direskeneli, H., Grayson, P. C., Jiang, L., Merkel, P. A., Saruhan-Direskeneli, G., Sawalha, A. H., Tombetti, E., Quaglia, A., Thorburn, D., Knight, J. C., Rochford, A. P., Murray, C. D., Divakar, P., Green, M., Nye, E., MacRae, J. I., Jamieson, N. B., Skoglund, P., Cader, M. Z., Wallace, C., Thomas, D. C., Lee, J. C.

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C13orf31 (FAMIN) is a central regulator of immunometabolic function von Cader, M Zaeem, Boroviak, Katharina, Zhang, Qifeng, Assadi, Ghazaleh, Kempster, Sarah L, Sewell, Gavin W, Saveljeva, Svetlana, Ashcroft, Jonathan W, Clare, Simon, Mukhopadhyay, Subhankar, Brown, Karen P, Tschurtschenthaler, Markus, Raine, Tim, Doe, Brendan, Chilvers, Edwin R, Griffin, Jules L, Kaneider, Nicole C, Floto, R Andres, D'Amato, Mauro, Bradley, Allan, Wakelam, Michael J O, Dougan, Gordon, Kaser, Arthur

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Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene von DYMENT, David A, CADER, M. Zameel, MONTPETIT, Alexandre, EBERS, George C, RAMAGOPALAN, Sreeram V, CHAO, Michael J, LINCOLN, Matthew R, MORRISON, Katie M, DISANTO, Giulio, MORAHAN, Julia M, DE LUCA, Gabriele C, DESSA SADOVNICK, A, LEPAGE, Pierre

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PTU-236 Endoscopic retrograde cholangiopancreatography (ERCP) metal biliary stent insertions: outcome and complications von Cader, M Z, James, M W

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PTU-236Endoscopic retrograde cholangiopancreatography (ERCP) metal biliary stent insertions: outcome and complications von Cader, M Z, James, M W

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