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Jamie McDonald

Showing results (31-40 of 57) with videos related to

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Orphanet Journal of Rare Diseases|December 24, 2011
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasiaKristy Damjanovich, Carmen Langa, Francisco J Blanco, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 25, 2022
A rare neuromyelitis optica mimic: Primary CNS histiocytic sarcomaDavid S Rogawski, Jeffrey J Nirschl, Jamie McDonald, et al.
Laryngoscope Investigative Otolaryngology|August 1, 2018
The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasiaRhett S Thomson, Nicole L Molin, Kevin J Whitehead, et al.
Journal of Neurosurgery. Pediatrics|June 5, 2012
Spinal arteriovenous fistulas in children with hereditary hemorrhagic telangiectasiaAmy R U L Calhoun, Robert J Bollo, Sarah T Garber, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 28, 2018
Clinical presentation and treatment paradigms of brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasiaNicholas T Gamboa, Evan J Joyce, Ilyas Eli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2014
Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart reviewKaren E Wain, Marissa S Ellingson, Jamie McDonald, et al.
Journal of Psychosocial Oncology|April 19, 2006
Patient-physician communication regarding use of complementary therapies during cancer treatmentCleora S Roberts, Frank Baker, Danette Hann, et al.
Science Signaling|January 18, 2018
Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasiaXuan Jiang, Whitney L Wooderchak-Donahue, Jamie McDonald, et al.
Plos One|October 17, 2013
Multiple sclerosis susceptibility genes: associations with relapse severity and recoveryEllen M Mowry, Robert F Carey, Maria R Blasco, et al.
Plos One|October 17, 2013
Association of multiple sclerosis susceptibility variants and early attack location in the CNSEllen M Mowry, Robert F Carey, Maria R Blasco, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Orphanet Journal of Rare Diseases|December 24, 2011
5'UTR mutations of ENG cause hereditary hemorrhagic telangiectasiaKristy Damjanovich, Carmen Langa, Francisco J Blanco, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|July 25, 2022
A rare neuromyelitis optica mimic: Primary CNS histiocytic sarcomaDavid S Rogawski, Jeffrey J Nirschl, Jamie McDonald, et al.
Laryngoscope Investigative Otolaryngology|August 1, 2018
The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasiaRhett S Thomson, Nicole L Molin, Kevin J Whitehead, et al.
Journal of Neurosurgery. Pediatrics|June 5, 2012
Spinal arteriovenous fistulas in children with hereditary hemorrhagic telangiectasiaAmy R U L Calhoun, Robert J Bollo, Sarah T Garber, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 28, 2018
Clinical presentation and treatment paradigms of brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasiaNicholas T Gamboa, Evan J Joyce, Ilyas Eli, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2014
Appreciating the broad clinical features of SMAD4 mutation carriers: a multicenter chart reviewKaren E Wain, Marissa S Ellingson, Jamie McDonald, et al.
Journal of Psychosocial Oncology|April 19, 2006
Patient-physician communication regarding use of complementary therapies during cancer treatmentCleora S Roberts, Frank Baker, Danette Hann, et al.
Science Signaling|January 18, 2018
Inactivating mutations in Drosha mediate vascular abnormalities similar to hereditary hemorrhagic telangiectasiaXuan Jiang, Whitney L Wooderchak-Donahue, Jamie McDonald, et al.
Plos One|October 17, 2013
Multiple sclerosis susceptibility genes: associations with relapse severity and recoveryEllen M Mowry, Robert F Carey, Maria R Blasco, et al.
Plos One|October 17, 2013
Association of multiple sclerosis susceptibility variants and early attack location in the CNSEllen M Mowry, Robert F Carey, Maria R Blasco, et al.
Pageof 6