Hakutulokset - Dyment, David

What is Next for the Genetics of Multiple Sclerosis? Tekijä Ramagopalan, Sreeram V., Dyment, David A.

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Multiple Sclerosis Tekijä Ramagopalan, Sreeram, Dyment, David, Farrell, Rachel, Isobe, Noriko

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The Benefit of Multigene Panel Testing for the Diagnosis and Management of the Genetic Epilepsies Tekijä Leduc-Pessah, Heather, White-Brown, Alexandre, Hartley, Taila, Pohl, Daniela, Dyment, David A.

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Atypical Rett Syndrome and Intractable Epilepsy With Novel GRIN2B Mutation Tekijä Kyriakopoulos, Paulina, McNiven, Vanda, Carter, Melissa T., Humphreys, Peter, Dyment, David, Fantaneanu, Tadeu A.

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Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature Tekijä Luco, Stephanie M., Pohl, Daniela, Sell, Erick, Wagner, Justin D., Dyment, David A., Daoud, Hussein

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Age of Onset in Concordant Twins and Other Relative Pairs With Multiple Sclerosis Tekijä Sadovnick, A. Dessa, Yee, Irene M., Guimond, Colleen, Reis, Jacques, Dyment, David A., Ebers, George C.

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Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings Tekijä Ferreira, Patrick, Luco, Stephanie M., Sawyer, Sarah L., Davila, Jorge, Boycott, Kym M., Dyment, David A.

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Evidence of Linkage with HLA-DR in DRB1*15-Negative Families with Multiple Sclerosis Tekijä Ligers, Arturs, Dyment, David A., Willer, Cristen J., Sadovnick, A. Dessa, Ebers, George, Risch, Neil, Hillert, Jan

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Timing of birth and risk of multiple sclerosis: population based study Tekijä Willer, Cristen J, Dyment, David A, Sadovnick, A Dessa, Rothwell, Peter M, Murray, T Jock, Ebers, George C

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An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene Tekijä Ramagopalan, Sreeram V, McMahon, Roisin, Dyment, David A, Sadovnick, A Dessa, Ebers, George C, Wittkowski, Knut M

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Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care Tekijä Hamilton, Alison, Tétreault, Martine, Dyment, David A., Zou, Ruobing, Kernohan, Kristin, Geraghty, Michael T., Hartley, Taila, Boycott, Kym M.

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A splice variant in ATAD3A expands the clinical and genetic spectrum of Harel-Yoon syndrome Tekijä Hanes, Ilana, McMillan, Hugh J., Ito, Yoko, Kernohan, Kristin D., Lazier, Joanna, Lines, Matthew A., Dyment, David A.

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Congenital Abnormalities and Multiple Sclerosis Tekijä Ramagopalan, Sreeram V, Guimond, Colleen, Criscuoli, Maria, Dyment, David A, Orton, Sarah-Michelle, Yee, Irene M, Ebers, George C, Sadovnick, Dessa

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Lysosomal dysfunction in TMEM106B hypomyelinating leukodystrophy Tekijä Ito, Yoko, Hartley, Taila, Baird, Stephen, Venkateswaran, Sunita, Simons, Cas, Wolf, Nicole I., Boycott, Kym M., Dyment, David A., Kernohan, Kristin D.

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No effect of preterm birth on the risk of multiple sclerosis: a population based study Tekijä Ramagopalan, Sreeram V, Valdar, William, Dyment, David A, DeLuca, Gabriele C, Orton, Sarah-Michelle, Yee, Irene M, Criscuoli, Maria, Ebers, George C, Sadovnick, A Dessa

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Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility Tekijä Lincoln, Matthew R., Ramagopalan, Sreeram V., Chao, Michael J., Herrera, Blanca M., DeLuca, Gabriele C., Orton, Sarah-Michelle, Dyment, David A., Sadovnick, A Dessa, Ebers, George C.

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Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype Tekijä Sawyer, Sarah L., Tian, Lei, Kähkönen, Marketta, Schwartzentruber, Jeremy, Kircher, Martin, Majewski, Jacek, Dyment, David A., Innes, A. Micheil, Boycott, Kym M., Moreau, Lisa A., Moilanen, Jukka S., Greenberg, Roger A.

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The Inheritance of Resistance Alleles in Multiple Sclerosis Tekijä Ramagopalan, Sreeram V, Morris, Andrew P, Dyment, David A, Herrera, Blanca M, DeLuca, Gabriele C, Lincoln, Matthew R, Orton, Sarah M, Chao, Michael J, Sadovnick, A. Dessa, Ebers, George C

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HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility Tekijä Chao, Michael J., Barnardo, Martin C. N. M., Lincoln, Matthew R., Ramagopalan, Sreeram V., Herrera, Blanca M., Dyment, David A., Montpetit, Alexandre, Sadovnick, A. Dessa, Knight, Julian C., Ebers, George C.

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Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis Tekijä Ramagopalan, Sreeram V, Dyment, David A, Morrison, Katie M, Herrera, Blanca M, DeLuca, Gabriele C, Lincoln, Matthew R, Orton, Sarah M, Handunnetthi, Lahiru, Chao, Michael J, Sadovnick, A Dessa, Ebers, George C

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