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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 15, 2017
Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons
Cindy Maurel, Blandine Madji-Hounoum, Rose-Anne Thepault, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 20, 2024
Sweet ending: When genetics prevent a dramatic CDG diagnostic mistake
Antoine Civit, Paul Gueguen, Helene Blasco, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2012
Homozygous SMN2 deletion is a protective factor in the Swedish ALS population
Philippe Corcia, Caroline Ingre, Helene Blasco, et al.
Annals of Clinical Biochemistry
|
February 2, 2018
Post hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability
Jean-Baptiste Delaye, Franck Patin, Emmanuelle Lagrue, et al.
BMC Pulmonary Medicine
|
March 8, 2020
Predicting the microbial cause of community-acquired pneumonia: can physicians or a data-driven method differentiate viral from bacterial pneumonia at patient presentation?
Claire Lhommet, Denis Garot, Leslie Grammatico-Guillon, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
March 2, 2018
Phenotypic and genotypic studies of ALS cases in ALS-SMA families
Philippe Corcia, Patrick Vourc'h, Helene Blasco, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
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Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
July 15, 2017
Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons
Cindy Maurel, Blandine Madji-Hounoum, Rose-Anne Thepault, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 20, 2024
Sweet ending: When genetics prevent a dramatic CDG diagnostic mistake
Antoine Civit, Paul Gueguen, Helene Blasco, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2012
Homozygous SMN2 deletion is a protective factor in the Swedish ALS population
Philippe Corcia, Caroline Ingre, Helene Blasco, et al.
Annals of Clinical Biochemistry
|
February 2, 2018
Post hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability
Jean-Baptiste Delaye, Franck Patin, Emmanuelle Lagrue, et al.
BMC Pulmonary Medicine
|
March 8, 2020
Predicting the microbial cause of community-acquired pneumonia: can physicians or a data-driven method differentiate viral from bacterial pneumonia at patient presentation?
Claire Lhommet, Denis Garot, Leslie Grammatico-Guillon, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
March 2, 2018
Phenotypic and genotypic studies of ALS cases in ALS-SMA families
Philippe Corcia, Patrick Vourc'h, Helene Blasco, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles
Laura Le Gall, William J Duddy, Cecile Martinat, et al.
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of 2