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P Rowland

Showing results (321-330 of 329) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Peer recommendations on how to improve clinical research, and Conference wrap-upDavid A Chad, Lewis P Rowland, Carmel Armon, et al.
Annals of Neurology|April 1, 1996
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophyK C Wilhelmsen, D M Blake, T Lynch, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
Neurology|April 25, 2007
Quantitative objective markers for upper and lower motor neuron dysfunction in ALSH Mitsumoto, A M Ulug, S L Pullman, et al.
Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Blood Advances|September 23, 2021
Clinical impact of NPM1-mutant molecular persistence after chemotherapy for acute myeloid leukemiaIng S Tiong, Richard Dillon, Adam Ivey, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 4, 2013
ALS Untangled No. 20: the Deanna protocol, Christina Fournier, Bedlack Bedlack, et al.
Pageof 33

Showing results (321-330 of 329) with videos related to

Sort By:
Pageof 33
You have reached the last page of results.This site can display upto 329 results.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Peer recommendations on how to improve clinical research, and Conference wrap-upDavid A Chad, Lewis P Rowland, Carmel Armon, et al.
Annals of Neurology|April 1, 1996
Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophyK C Wilhelmsen, D M Blake, T Lynch, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
Neurology|April 25, 2007
Quantitative objective markers for upper and lower motor neuron dysfunction in ALSH Mitsumoto, A M Ulug, S L Pullman, et al.
Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Blood Advances|September 23, 2021
Clinical impact of NPM1-mutant molecular persistence after chemotherapy for acute myeloid leukemiaIng S Tiong, Richard Dillon, Adam Ivey, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 4, 2013
ALS Untangled No. 20: the Deanna protocol, Christina Fournier, Bedlack Bedlack, et al.
Pageof 33