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Bharucha

Showing results (751-760 of 791) with videos related to

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Journal of Cachexia, Sarcopenia and Muscle|September 4, 2022
Water T2 could predict functional decline in patients with dysferlinopathyUrsula Moore, Ericky Caldas de Almeida Araújo, Harmen Reyngoudt, et al.
Humanities & Social Sciences Communications|July 6, 2022
An agenda for future Social Sciences and Humanities research on energy efficiency: 100 priority research questionsChris Foulds, Sarah Royston, Thomas Berker, et al.
Neuromuscular Disorders : NMD|February 21, 2021
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same diseaseUrsula Moore, Heather Gordish, Jordi Diaz-Manera, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
PIEZO2-dependent rapid pain system in humans and miceOtmane Bouchatta, Marek Brodzki, Houria Manouze, et al.
International Journal of Cardiology|September 30, 2023
Sudden cardiac death in childhood RASopathy-associated hypertrophic cardiomyopathy: Validation of the HCM risk-kids model and predictors of eventsOlga D Boleti, Sotirios Roussos, Gabrielle Norrish, et al.
The Lancet. Infectious Diseases|August 10, 2020
STROBE-metagenomics: a STROBE extension statement to guide the reporting of metagenomics studiesTehmina Bharucha, Clarissa Oeser, Francois Balloux, et al.
Journal of Neuromuscular Diseases|March 22, 2021
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related MyopathiesRocío N Villar-Quiles, Sandra Donkervoort, Alix de Becdelièvre, et al.
EMBO Molecular Medicine|November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsySandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
American Journal of Human Genetics|May 5, 2018
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor NeuronopathyDavid T Burns, Sandra Donkervoort, Juliane S Müller, et al.
Journal of the Endocrine Society|January 9, 2026
Adrenal Suppression in Duchenne Muscular Dystrophy: Management Strategies Incorporating Novel Steroid VamoroloneAnne Marie Sbrocchi, Kathi Kinnett, Maria-Elena Lautatzis, et al.
Pageof 80

Showing results (751-760 of 791) with videos related to

Sort By:
Pageof 80
Journal of Cachexia, Sarcopenia and Muscle|September 4, 2022
Water T2 could predict functional decline in patients with dysferlinopathyUrsula Moore, Ericky Caldas de Almeida Araújo, Harmen Reyngoudt, et al.
Humanities & Social Sciences Communications|July 6, 2022
An agenda for future Social Sciences and Humanities research on energy efficiency: 100 priority research questionsChris Foulds, Sarah Royston, Thomas Berker, et al.
Neuromuscular Disorders : NMD|February 21, 2021
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same diseaseUrsula Moore, Heather Gordish, Jordi Diaz-Manera, et al.
Biorxiv : the Preprint Server for Biology|January 3, 2024
PIEZO2-dependent rapid pain system in humans and miceOtmane Bouchatta, Marek Brodzki, Houria Manouze, et al.
International Journal of Cardiology|September 30, 2023
Sudden cardiac death in childhood RASopathy-associated hypertrophic cardiomyopathy: Validation of the HCM risk-kids model and predictors of eventsOlga D Boleti, Sotirios Roussos, Gabrielle Norrish, et al.
The Lancet. Infectious Diseases|August 10, 2020
STROBE-metagenomics: a STROBE extension statement to guide the reporting of metagenomics studiesTehmina Bharucha, Clarissa Oeser, Francois Balloux, et al.
Journal of Neuromuscular Diseases|March 22, 2021
Clinical and Molecular Spectrum Associated with COL6A3 c.7447A>G p.(Lys2483Glu) Variant: Elucidating its Role in Collagen VI-related MyopathiesRocío N Villar-Quiles, Sandra Donkervoort, Alix de Becdelièvre, et al.
EMBO Molecular Medicine|November 15, 2021
BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsySandra Donkervoort, Niklas Krause, Mykola Dergai, et al.
American Journal of Human Genetics|May 5, 2018
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor NeuronopathyDavid T Burns, Sandra Donkervoort, Juliane S Müller, et al.
Journal of the Endocrine Society|January 9, 2026
Adrenal Suppression in Duchenne Muscular Dystrophy: Management Strategies Incorporating Novel Steroid VamoroloneAnne Marie Sbrocchi, Kathi Kinnett, Maria-Elena Lautatzis, et al.
Pageof 80