Search research articles
Contact Us
Filters
Showing results (41-50 of 57) with videos related to
Page
of 6
Sort By:
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 6, 2018
Clinical presentation and treatment paradigms in patients with hereditary hemorrhagic telangiectasia and spinal vascular malformations
Ilyas Eli, Nicholas T Gamboa, Evan J Joyce, et al.
Integrative Cancer Therapies
|
May 11, 2006
Exercise use as complementary therapy among breast and prostate cancer survivors receiving active treatment: examination of exercise intention
Tiffany T Hunt-Shanks, Chris M Blanchard, Frank Baker, et al.
Neurology
|
January 2, 2024
Prevalence, Demographic, and Clinical Factors Associated With Cognitive Dysfunction in Patients With Neuromyelitis Optica Spectrum Disorder
Luka Vlahovic, Jamie McDonald, Jessica Hinman, et al.
Journal of Neuropathology and Experimental Neurology
|
June 2, 2026
Multiparameter flow cytometry of CSF identifies elevated CD8+ effector memory and TEMRA T-cells in immune-mediated neurologic disorders
Danwei Wu, Samuel Zhang, Yaseen Ali Jamal, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2003
Genetic testing for a BRCA1 mutation: prophylactic surgery and screening behavior in women 2 years post testing
Jeffrey R Botkin, Ken R Smith, Robert T Croyle, et al.
Journal of Clinical Medicine
|
December 9, 2023
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. <i>J. Clin. Med.</i> 2023, <i>12</i>, 2704"
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Journal of Clinical Medicine
|
April 13, 2023
Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Journal of Medical Genetics
|
September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic Telangiectasia
Whitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Molecular Genetics & Genomic Medicine
|
April 9, 2021
Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children
Joshua Hodgson, Lidia Ruiz-Llorente, Jamie McDonald, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2018
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation
Whitney L Wooderchak-Donahue, Peter Johnson, Jamie McDonald, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
February 6, 2018
Clinical presentation and treatment paradigms in patients with hereditary hemorrhagic telangiectasia and spinal vascular malformations
Ilyas Eli, Nicholas T Gamboa, Evan J Joyce, et al.
Integrative Cancer Therapies
|
May 11, 2006
Exercise use as complementary therapy among breast and prostate cancer survivors receiving active treatment: examination of exercise intention
Tiffany T Hunt-Shanks, Chris M Blanchard, Frank Baker, et al.
Neurology
|
January 2, 2024
Prevalence, Demographic, and Clinical Factors Associated With Cognitive Dysfunction in Patients With Neuromyelitis Optica Spectrum Disorder
Luka Vlahovic, Jamie McDonald, Jessica Hinman, et al.
Journal of Neuropathology and Experimental Neurology
|
June 2, 2026
Multiparameter flow cytometry of CSF identifies elevated CD8+ effector memory and TEMRA T-cells in immune-mediated neurologic disorders
Danwei Wu, Samuel Zhang, Yaseen Ali Jamal, et al.
American Journal of Medical Genetics. Part A
|
April 4, 2003
Genetic testing for a BRCA1 mutation: prophylactic surgery and screening behavior in women 2 years post testing
Jeffrey R Botkin, Ken R Smith, Robert T Croyle, et al.
Journal of Clinical Medicine
|
December 9, 2023
Reply to Eker et al. Comment on "Kilian et al. Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT. <i>J. Clin. Med.</i> 2023, <i>12</i>, 2704"
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Journal of Clinical Medicine
|
April 13, 2023
Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT
Alexandra Kilian, Giuseppe A Latino, Andrew J White, et al.
Journal of Medical Genetics
|
September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic Telangiectasia
Whitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Molecular Genetics & Genomic Medicine
|
April 9, 2021
Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children
Joshua Hodgson, Lidia Ruiz-Llorente, Jamie McDonald, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2018
Expanding the clinical and molecular findings in RASA1 capillary malformation-arteriovenous malformation
Whitney L Wooderchak-Donahue, Peter Johnson, Jamie McDonald, et al.
Page
of 6