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E Flanagan

Showing results (291-300 of 582) with videos related to

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Internal Medicine Journal|July 22, 2014
A novel hepatitis B virus S gene insertion associated with reduced humoral immunity and diagnostic escapeE Flanagan, A J Thompson, D Colledge, et al.
Journal of Alzheimer'S Disease : JAD|July 31, 2023
Neuropathologic Changes of Alzheimer's Disease and Related Dementias: Relevance to Future PreventionLon R White, Maria M Corrada, Claudia H Kawas, et al.
Journal of Biomedical Informatics|August 3, 2018
A cognitive systems engineering design approach to improve the usability of electronic order forms for medical consultationApril Savoy, Laura G Militello, Himalaya Patel, et al.
Clinical Endocrinology|September 22, 2018
Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemiaThomas W Laver, Matthew N Wakeling, Janet Hong Yeow Hua, et al.
Orphanet Journal of Rare Diseases|May 16, 2012
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA DehydrogenaseAmanda J Heslegrave, Ritika R Kapoor, Simon Eaton, et al.
Frontiers in Oncology|May 27, 2024
Incidence and risk factors for bone metastases at presentation in solid tumorsBrendan J Knapp, Giordano F Cittolin-Santos, Mary E Flanagan, et al.
Joint Commission Journal on Quality and Patient Safety|August 4, 2018
"Workin' on Our Night Moves": How Residents Prepare for Shift HandoffsLaura G Militello, Nicholas A Rattray, Mindy E Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 2007
Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblingsEmma L Edghill, Anna L Gloyn, Anne Goriely, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2011
The heterogeneity of focal forms of congenital hyperinsulinismDunia Ismail, Ritika R Kapoor, Virpi V Smith, et al.
Pediatric Blood & Cancer|March 21, 2013
Thiamine responsive megaloblastic anemia with a novel SLC19A2 mutation presenting with myeloid maturational arrestVikas Dua, Satya P Yadav, Vijay Kumar, et al.
Pageof 59

Showing results (291-300 of 582) with videos related to

Sort By:
Pageof 59
Internal Medicine Journal|July 22, 2014
A novel hepatitis B virus S gene insertion associated with reduced humoral immunity and diagnostic escapeE Flanagan, A J Thompson, D Colledge, et al.
Journal of Alzheimer'S Disease : JAD|July 31, 2023
Neuropathologic Changes of Alzheimer's Disease and Related Dementias: Relevance to Future PreventionLon R White, Maria M Corrada, Claudia H Kawas, et al.
Journal of Biomedical Informatics|August 3, 2018
A cognitive systems engineering design approach to improve the usability of electronic order forms for medical consultationApril Savoy, Laura G Militello, Himalaya Patel, et al.
Clinical Endocrinology|September 22, 2018
Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemiaThomas W Laver, Matthew N Wakeling, Janet Hong Yeow Hua, et al.
Orphanet Journal of Rare Diseases|May 16, 2012
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA DehydrogenaseAmanda J Heslegrave, Ritika R Kapoor, Simon Eaton, et al.
Frontiers in Oncology|May 27, 2024
Incidence and risk factors for bone metastases at presentation in solid tumorsBrendan J Knapp, Giordano F Cittolin-Santos, Mary E Flanagan, et al.
Joint Commission Journal on Quality and Patient Safety|August 4, 2018
"Workin' on Our Night Moves": How Residents Prepare for Shift HandoffsLaura G Militello, Nicholas A Rattray, Mindy E Flanagan, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 2007
Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblingsEmma L Edghill, Anna L Gloyn, Anne Goriely, et al.
The Journal of Clinical Endocrinology and Metabolism|October 28, 2011
The heterogeneity of focal forms of congenital hyperinsulinismDunia Ismail, Ritika R Kapoor, Virpi V Smith, et al.
Pediatric Blood & Cancer|March 21, 2013
Thiamine responsive megaloblastic anemia with a novel SLC19A2 mutation presenting with myeloid maturational arrestVikas Dua, Satya P Yadav, Vijay Kumar, et al.
Pageof 59