Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anthony C. Torres"'
Publikováno v:
Cogent Medicine, Vol 8, Iss 1 (2021)
Abstract: Thirty-three-year-old Caucasian male underwent initiation of levetiracetam following witnessed generalized seizure activity at the same time presenting with a right MCA territory ischemic stroke. He then developed elevated CPK and myalgias
Externí odkaz:
https://doaj.org/article/2cc2ab330fdb4f21b34566da700073e0
Publikováno v:
Interdisciplinary Neurosurgery, Vol 10, Iss , Pp 155-158 (2017)
Cowden disease is a rare autosomal dominant disorder first described by Rachel Cowden in 1963 as one of the phosphatase and tensin homolog (PTEN) gene hamartoma tumor syndromes. Commonly affecting multiple systems, patients typically have an increase
Externí odkaz:
https://doaj.org/article/48b8e9f2c2d4469d9a13e14ac406978e
Publikováno v:
Cogent Medicine, Vol 5, Iss 1 (2018)
Multiple systems atrophy (MSA) describes a group of rare neurodegenerative disorders classified as Parkinsonism predominant (MSA-P) or cerebellar ataxia (MSA-C) subtypes. Parkinsonism or cerebellar ataxia is frequently the initial motor symptom; it i
Externí odkaz:
https://doaj.org/article/6b01dcdd78c4438088e1d63062cd5e1b
Publikováno v:
Cogent Medicine, Vol 8, Iss 1 (2021)
Thirty-three-year-old Caucasian male underwent initiation of levetiracetam following witnessed generalized seizure activity at the same time presenting with a right MCA territory ischemic stroke. He then developed elevated CPK and myalgias are highly
Publikováno v:
Cogent Medicine, Vol 5, Iss 1 (2018)
Multiple systems atrophy (MSA) describes a group of rare neurodegenerative disorders classified as Parkinsonism predominant (MSA-P) or cerebellar ataxia (MSA-C) subtypes. Parkinsonism or cerebellar ataxia is frequently the initial motor symptom; it i
Autor:
Lori Friedman, Kyla M. Grimshaw, Sabrina Arena, Anthony C. Torres, Alberto Bardelli, Jeffrey Eastham-Anderson, Christopher Torrance, Peter M. Haverty, Sue Griffin, Jeffrey Wallin, Klaus P. Hoeflich, Kyle A. Edgar, Marcia Belvin, Jane Guan, John Goodall, Wei Zhou, Ross Francis
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 5, p e36402 (2012)
PLoS ONE, Vol 7, Iss 5, p e36402 (2012)
The PTEN/PI3K pathway is commonly mutated in cancer and therefore represents an attractive target for therapeutic intervention. To investigate the primary phenotypes mediated by increased pathway signaling in a clean, patient-relevant context, an act
Autor:
Jeffrey J Wallin, Jane Guan, Kyle A Edgar, Wei Zhou, Ross Francis, Anthony C Torres, Peter M Haverty, Jeffrey Eastham-Anderson, Sabrina Arena, Alberto Bardelli, Sue Griffin, John E Goodall, Kyla M Grimshaw, Klaus P Hoeflich, Christopher Torrance, Marcia Belvin, Lori S Friedman
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e36402 (2012)
The PTEN/PI3K pathway is commonly mutated in cancer and therefore represents an attractive target for therapeutic intervention. To investigate the primary phenotypes mediated by increased pathway signaling in a clean, patient-relevant context, an act
Externí odkaz:
https://doaj.org/article/64952bf9ee0a4f75af0606c666386285