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Journal of General Internal Medicine
|
April 7, 2021
Did the 2015 USPSTF Abnormal Blood Glucose Recommendations Change Clinician Attitudes or Behaviors? A Mixed-Method Assessment
Tainayah W Thomas, Carol E Golin, Alan C Kinlaw, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1985
The postoperative fibrinolytic shutdown: a rapidly reverting acute phase pattern for the fast-acting inhibitor of tissue-type plasminogen activator after trauma
C Kluft, J H Verheijen, A F Jie, et al.
Annals of Neurology
|
June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
A L Andreu, K Tanji, C Bruno, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
June 9, 2025
The Burden of Mitochondrial Disease: Healthcare and Societal Costs
Deborah Schofield, Katherine Lim, Owen Tan, et al.
Clinical & Experimental Metastasis
|
September 22, 2014
Gene expression accurately distinguishes liver metastases of small bowel and pancreas neuroendocrine tumors
Scott K Sherman, Jessica E Maxwell, Jennifer C Carr, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
January 31, 2021
Addition of <sup>131</sup>I-MIBG to PRRT (<sup>90</sup>Y-DOTATOC) for Personalized Treatment of Selected Patients with Neuroendocrine Tumors
David L Bushnell, Kellie L Bodeker, Thomas M O'Dorisio, et al.
Annals of Surgical Oncology
|
October 12, 2013
Overexpression of membrane proteins in primary and metastatic gastrointestinal neuroendocrine tumors
Jennifer C Carr, Scott K Sherman, Donghong Wang, et al.
American Journal of Surgery
|
July 6, 2000
Relaparoscopy for the detection and treatment of complications of laparoscopic cholecystectomy
S P Dexter, G V Miller, D Davides, et al.
Pediatric Research
|
January 23, 2003
Mutation screening in patients with isolated cytochrome c oxidase deficiency
Sabrina Sacconi, Leonardo Salviati, Carolyn M Sue, et al.
Journal of Inherited Metabolic Disease
|
December 21, 2016
A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders
Lisa G Riley, Mark J Cowley, Velimir Gayevskiy, et al.
Page
of 42
Search research articles
Search
Showing results (261-270 of 415) with videos related to
Sort By:
Page
of 42
Journal of General Internal Medicine
|
April 7, 2021
Did the 2015 USPSTF Abnormal Blood Glucose Recommendations Change Clinician Attitudes or Behaviors? A Mixed-Method Assessment
Tainayah W Thomas, Carol E Golin, Alan C Kinlaw, et al.
Scandinavian Journal of Clinical and Laboratory Investigation
|
November 1, 1985
The postoperative fibrinolytic shutdown: a rapidly reverting acute phase pattern for the fast-acting inhibitor of tissue-type plasminogen activator after trauma
C Kluft, J H Verheijen, A F Jie, et al.
Annals of Neurology
|
June 9, 1999
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene
A L Andreu, K Tanji, C Bruno, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research
|
June 9, 2025
The Burden of Mitochondrial Disease: Healthcare and Societal Costs
Deborah Schofield, Katherine Lim, Owen Tan, et al.
Clinical & Experimental Metastasis
|
September 22, 2014
Gene expression accurately distinguishes liver metastases of small bowel and pancreas neuroendocrine tumors
Scott K Sherman, Jessica E Maxwell, Jennifer C Carr, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
January 31, 2021
Addition of <sup>131</sup>I-MIBG to PRRT (<sup>90</sup>Y-DOTATOC) for Personalized Treatment of Selected Patients with Neuroendocrine Tumors
David L Bushnell, Kellie L Bodeker, Thomas M O'Dorisio, et al.
Annals of Surgical Oncology
|
October 12, 2013
Overexpression of membrane proteins in primary and metastatic gastrointestinal neuroendocrine tumors
Jennifer C Carr, Scott K Sherman, Donghong Wang, et al.
American Journal of Surgery
|
July 6, 2000
Relaparoscopy for the detection and treatment of complications of laparoscopic cholecystectomy
S P Dexter, G V Miller, D Davides, et al.
Pediatric Research
|
January 23, 2003
Mutation screening in patients with isolated cytochrome c oxidase deficiency
Sabrina Sacconi, Leonardo Salviati, Carolyn M Sue, et al.
Journal of Inherited Metabolic Disease
|
December 21, 2016
A SLC39A8 variant causes manganese deficiency, and glycosylation and mitochondrial disorders
Lisa G Riley, Mark J Cowley, Velimir Gayevskiy, et al.
Page
of 42