Torthaí cuardaigh - Daniel Darvish
- 1 - 3 toradh as 3 á dtaispeáint
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1
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein de réir Giles D. Watts, Jill Wymer, Margaret J. Kovach, Sarju Mehta, Steven Mumm, Daniel Darvish, Alan Pestronk, Michael P. Whyte, Virginia Kimonis
Foilsithe / Cruthaithe 2004Artigo -
2
Mutation in the key enzyme of sialic acid biosynthesis causes severe glomerular proteinuria and is rescued by N-acetylmannosamine de réir Belinda Galeano, Riko Klootwijk, Irini Manoli, MaoSen Sun, Carla Ciccone, Daniel Darvish, Matthew F. Starost, Patricia M. Zerfas, Victoria Hoffmann, Shelley Hoogstraten-Miller, Donna M. Krasnewich, William A. Gahl, Marjan Huizing
Foilsithe / Cruthaithe 2007Artigo -
3
Limb-Girdle Muscular Dystrophy in the United States de réir Steven A. Moore, Christopher Shilling, Steven Westra, Cheryl Wall, Matthew Wicklund, Catherine A. Stolle, Charlotte A. Brown, Daniel E. Michele, F. Piccolo, Thomas Winder, Aaron A. Stence, Rita Barresi, Nick King, Wendy King, Julaine Florence, Kevin P. Campbell, Gerald M. Fenichel, Hansell H. Stedman, John T. Kissel, Robert C. Griggs, Shree Pandya, Katherine D. Mathews, Alan Pestronk, Carmen Serrano, Daniel Darvish, Jerry R. Mendell
Foilsithe / Cruthaithe 2006Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Gene
Medicine
Mutation
Biology
Genetics
Pathology
Biochemistry
Bioinformatics
Biopsy
Biosynthesis
Cancer research
Chemistry
Dementia
Disease
Endocrinology
Environmental health
Enzyme
Frontotemporal dementia
Genotype
Histopathology
Internal medicine
Kidney
Limb-girdle muscular dystrophy
Missense mutation
Muscle biopsy
Muscular dystrophy
Myopathy
N-Acetylneuraminic acid
Paget's disease of bone
Population