Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Veeral Katheria"'
Autor:
Angèle Nalbandian, Christopher Nguyen, Veeral Katheria, Katrina J Llewellyn, Mallikarjun Badadani, Vincent Caiozzo, Virginia E Kimonis
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76187 (2013)
The therapeutic effects of exercise resistance and endurance training in the alleviation of muscle hypertrophy/atrophy should be considered in the management of patients with advanced neuromuscular diseases. Patients with progressive neuromuscular di
Externí odkaz:
https://doaj.org/article/0107b613408b4fd2835c44f90efe35e6
Autor:
Katrina J. Llewellyn, Rachel Dec, B S Veeral Katheria, Virginia Kimonis, Shlomit Radom-Aizik, Lbachir BenMohamed, Manaswitha Khare, Szu-Yun Leu, Angèle Nalbandian, B S Prachi Rana, Frank Zaldivar, Eric Dec
Publikováno v:
Clinical and Translational Science. 7:29-32
Valosin containing protein (VCP) disease (also known as Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia [IBMPFD] syndrome) is caused by mutations in the gene encoding VCP classically affecting the muscle, bone and brain. Al
Autor:
Prachi Rana, Eric Dec, Virginia Kimonis, Katrina J. Llewellyn, Angèle Nalbandian, Bill Gross, Hans S. Keirstead, David Ferguson, Matthew Gargus, Abel Ibrahim, Veeral Katheria, Maya N. Hatch
Publikováno v:
Journal of Stem Cell Research & Therapy.
Valosin Containing Protein (VCP) disease is an autosomal dominant disorder caused by mutations in the VCP gene and is associated with progressive muscle weakness and atrophy. Affected individuals exhibit striking scapular winging due to shoulder gird
Autor:
Eric, Dec, Prachi, Rana, Veeral, Katheria, Rachel, Dec, Manaswitha, Khare, Angèle, Nalbandian, Szu-Yun, Leu, Shlomit, Radom-Aizik, Katrina, Llewellyn, Lbachir, BenMohamed, Frank, Zaldivar, Virginia, Kimonis
Publikováno v:
Clinical and translational science. 7(1)
Valosin containing protein (VCP) disease (also known as Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia [IBMPFD] syndrome) is caused by mutations in the gene encoding VCP classically affecting the muscle, bone and brain. Al
Autor:
Virginia Kimonis, Veeral Katheria, Angèle Nalbandian, Katrina J. Llewellyn, Christopher Nguyen, Vincent J. Caiozzo, Mallikarjun Badadani
Publikováno v:
Nalbandian, Angele; Nguyen, Christopher; Katheria, Veeral; Llewellyn, Katrina J.; Badadani, Mallikarjun; Caiozzo, Vincent; et al.(2013). Exercise Training Reverses Skeletal Muscle Atrophy in an Experimental Model of VCP Disease. PLoS ONE, 8(10). UC Irvine: Institute for Clinical and Translational Science. Retrieved from: http://www.escholarship.org/uc/item/9cz8j395
Nalbandian, A; Nguyen, C; Katheria, V; Llewellyn, KJ; Badadani, M; Caiozzo, V; et al.(2013). Exercise Training Reverses Skeletal Muscle Atrophy in an Experimental Model of VCP Disease. PLoS ONE, 8(10). doi: 10.1371/journal.pone.0076187. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3rj4j0wn
PLoS ONE, Vol 8, Iss 10, p e76187 (2013)
PloS one, vol 8, iss 10
PLoS ONE
Nalbandian, A; Nguyen, C; Katheria, V; Llewellyn, KJ; Badadani, M; Caiozzo, V; et al.(2013). Exercise Training Reverses Skeletal Muscle Atrophy in an Experimental Model of VCP Disease. PLoS ONE, 8(10). doi: 10.1371/journal.pone.0076187. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3rj4j0wn
PLoS ONE, Vol 8, Iss 10, p e76187 (2013)
PloS one, vol 8, iss 10
PLoS ONE
Background:The therapeutic effects of exercise resistance and endurance training in the alleviation of muscle hypertrophy/atrophy should be considered in the management of patients with advanced neuromuscular diseases. Patients with progressive neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::755d5d9b81f37275ac97889b0e9faf90
http://www.escholarship.org/uc/item/9cz8j395
http://www.escholarship.org/uc/item/9cz8j395
Autor:
Angèle, Nalbandian, Katrina J, Llewellyn, Mallikarjun, Badadani, Hong Z, Yin, Christopher, Nguyen, Veeral, Katheria, Giles, Watts, Jogeshwar, Mukherjee, Jouni, Vesa, Vincent, Caiozzo, Tahseen, Mozaffar, John H, Weiss, Virginia E, Kimonis
Publikováno v:
Musclenerve. 47(2)
Mutations in the valosin-containing protein (VCP) gene cause hereditary inclusion body myopathy (IBM) associated with Paget disease of bone (PDB), and frontotemporal dementia (FTD). More recently, these mutations have been linked to 2% of familial am
Autor:
Virginia Kimonis, Prachi Rana, Angèle Nalbandian, Veeral Katheria, Charles D. Smith, Jouni Vesa, Vincent J. Caiozzo, Jogeshwar Mukherjee, Mallikarjun Badadani, Sandra Donkervoort, Barbara Martin, Christopher Nguyen, Eric Dec, Giles D. J. Watts
Publikováno v:
Journal of molecular neuroscience : MN. 45(3)
Inclusion body myopathy associated with Paget’s disease of bone and frontotemporal dementia (IBMPFD) is a progressive, fatal genetic disorder with variable penetrance, predominantly affecting three main tissue types: muscle (IBM), bone (PDB), and b