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M Reilly

Showing results (1251-1260 of 1,622) with videos related to

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The Journal of Trauma and Acute Care Surgery|September 17, 2019
The impact of interhospital transfer on mortality benchmarking at Level III and IV trauma centers: A step toward shared mortality attribution in a statewide systemDaniel N Holena, Elinore J Kaufman, Justin Hatchimonji, et al.
Advances in Therapy|April 14, 2022
Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UKJulian D Gillmore, Mary M Reilly, Caroline J Coats, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 25, 2019
Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynaminTayyibah Ali, Joanna Bednarska, Stéphane Vassilopoulos, et al.
JAMA Surgery|May 21, 2015
Arteriography for Lower Gastrointestinal Hemorrhage: Role of Preceding Abdominal Computed Tomographic Angiogram in Diagnosis and LocalizationChristina L Jacovides, Gregory Nadolski, Steven R Allen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 7, 2012
Tremor in inflammatory neuropathiesTabish Aziz Saifee, Petra Schwingenschuh, Mary M Reilly, et al.
Surgery|September 1, 1985
Prostacyclin production in regions of arterial stenosisP G Qvarfordt, L M Reilly, R J Lusby, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Lupus Science & Medicine|May 7, 2026
Double humanised lupus mouse model with human immune system and faecal microbiota from patients with SLETian Xu, Ran Lu, David N Oakland, et al.
Annals of Clinical and Translational Neurology|February 17, 2025
Twelve-month change in quantitative MRI calf muscle fat fraction in CMT1A predicts clinical change over 4 yearsMatthew R B Evans, Hamza A Salhab, Christopher D J Sinclair, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Pageof 163

Showing results (1251-1260 of 1,622) with videos related to

Sort By:
Pageof 163
The Journal of Trauma and Acute Care Surgery|September 17, 2019
The impact of interhospital transfer on mortality benchmarking at Level III and IV trauma centers: A step toward shared mortality attribution in a statewide systemDaniel N Holena, Elinore J Kaufman, Justin Hatchimonji, et al.
Advances in Therapy|April 14, 2022
Clinical and Genetic Evaluation of People with or at Risk of Hereditary ATTR Amyloidosis: An Expert Opinion and Consensus on Best Practice in Ireland and the UKJulian D Gillmore, Mary M Reilly, Caroline J Coats, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 25, 2019
Correlative SICM-FCM reveals changes in morphology and kinetics of endocytic pits induced by disease-associated mutations in dynaminTayyibah Ali, Joanna Bednarska, Stéphane Vassilopoulos, et al.
JAMA Surgery|May 21, 2015
Arteriography for Lower Gastrointestinal Hemorrhage: Role of Preceding Abdominal Computed Tomographic Angiogram in Diagnosis and LocalizationChristina L Jacovides, Gregory Nadolski, Steven R Allen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 7, 2012
Tremor in inflammatory neuropathiesTabish Aziz Saifee, Petra Schwingenschuh, Mary M Reilly, et al.
Surgery|September 1, 1985
Prostacyclin production in regions of arterial stenosisP G Qvarfordt, L M Reilly, R J Lusby, et al.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Lupus Science & Medicine|May 7, 2026
Double humanised lupus mouse model with human immune system and faecal microbiota from patients with SLETian Xu, Ran Lu, David N Oakland, et al.
Annals of Clinical and Translational Neurology|February 17, 2025
Twelve-month change in quantitative MRI calf muscle fat fraction in CMT1A predicts clinical change over 4 yearsMatthew R B Evans, Hamza A Salhab, Christopher D J Sinclair, et al.
Neurology|September 16, 2016
SIGMAR1 mutation associated with autosomal recessive Silver-like syndromeAlejandro Horga, Pedro J Tomaselli, Michael A Gonzalez, et al.
Pageof 163