Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shamima Rahman

Showing results (41-50 of 182) with videos related to

Pageof 19
Sort By:
Developmental Medicine and Child Neurology|September 25, 2012
Inborn errors of metabolism causing epilepsyShamima Rahman, Emma J Footitt, Sophia Varadkar, et al.
Journal of Inherited Metabolic Disease|July 4, 2020
Moving towards clinical trials for mitochondrial diseasesRobert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 12, 2013
Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular featuresCarlotta Spagnoli, Matthew C Pitt, Shamima Rahman, et al.
Journal of Inherited Metabolic Disease|March 25, 2021
Editorial: Mitochondrial medicine special issuePatrick F Chinnery, Marni J Falk, Vamsi K Mootha, et al.
Molecular Genetics and Metabolism|February 1, 2026
Clinical and biochemical footprints of primary mitochondrial disorders: proposed nosologyMartina Messina, Rebecca Ganetzky, Carlos R Ferreira, et al.
Annals of Neurology|October 28, 2015
Leigh syndrome: One disorder, more than 75 monogenic causesNicole J Lake, Alison G Compton, Shamima Rahman, et al.
Neuromuscular Disorders : NMD|August 4, 2023
258th ENMC international workshop Leigh syndrome spectrum: genetic causes, natural history and preparing for clinical trials 25-27 March 2022, Hoofddorp, Amsterdam, The NetherlandsDaria Diodato, Manuel Schiff, Bruce H Cohen, et al.
Plos One|July 4, 2018
Near infrared spectroscopy with a vascular occlusion test as a biomarker in children with mitochondrial and other neuro-genetic disordersSainath Raman, Latifa Chentouf, Catherine DeVile, et al.
Journal of Inherited Metabolic Disease|December 11, 2022
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genesAzizia Wahedi, Chandika Soondram, Alan E Murphy, et al.
Pharmacological Research|March 10, 2024
IUPHAR ECR review: Cancer-related anorexia-cachexia in cancer patients: Pathophysiology and treatmentIftekhar Hossain Chowdhury, Shamima Rahman, Yeasmin Jahan Afroze, et al.
Pageof 19

Showing results (41-50 of 182) with videos related to

Sort By:
Pageof 19
Developmental Medicine and Child Neurology|September 25, 2012
Inborn errors of metabolism causing epilepsyShamima Rahman, Emma J Footitt, Sophia Varadkar, et al.
Journal of Inherited Metabolic Disease|July 4, 2020
Moving towards clinical trials for mitochondrial diseasesRobert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 12, 2013
Brown-Vialetto-van Laere syndrome: a riboflavin responsive neuronopathy of infancy with singular featuresCarlotta Spagnoli, Matthew C Pitt, Shamima Rahman, et al.
Journal of Inherited Metabolic Disease|March 25, 2021
Editorial: Mitochondrial medicine special issuePatrick F Chinnery, Marni J Falk, Vamsi K Mootha, et al.
Molecular Genetics and Metabolism|February 1, 2026
Clinical and biochemical footprints of primary mitochondrial disorders: proposed nosologyMartina Messina, Rebecca Ganetzky, Carlos R Ferreira, et al.
Annals of Neurology|October 28, 2015
Leigh syndrome: One disorder, more than 75 monogenic causesNicole J Lake, Alison G Compton, Shamima Rahman, et al.
Neuromuscular Disorders : NMD|August 4, 2023
258th ENMC international workshop Leigh syndrome spectrum: genetic causes, natural history and preparing for clinical trials 25-27 March 2022, Hoofddorp, Amsterdam, The NetherlandsDaria Diodato, Manuel Schiff, Bruce H Cohen, et al.
Plos One|July 4, 2018
Near infrared spectroscopy with a vascular occlusion test as a biomarker in children with mitochondrial and other neuro-genetic disordersSainath Raman, Latifa Chentouf, Catherine DeVile, et al.
Journal of Inherited Metabolic Disease|December 11, 2022
Transcriptomic analyses reveal neuronal specificity of Leigh syndrome associated genesAzizia Wahedi, Chandika Soondram, Alan E Murphy, et al.
Pharmacological Research|March 10, 2024
IUPHAR ECR review: Cancer-related anorexia-cachexia in cancer patients: Pathophysiology and treatmentIftekhar Hossain Chowdhury, Shamima Rahman, Yeasmin Jahan Afroze, et al.
Pageof 19