Suchergebnisse - Dyment, David

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

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Multiple Sclerosis von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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 von 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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