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T Warner

Showing results (111-120 of 403) with videos related to

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Journal of Women'S Health (2002)|March 31, 2017
Organizational Context and Female Faculty's Perception of the Climate for Women in Academic MedicineRené Carapinha, Caitlin M McCracken, Erica T Warner, et al.
Journal of Women'S Health (2002)|August 4, 2017
Gender Differences in Receipt of National Institutes of Health R01 Grants Among Junior Faculty at an Academic Medical Center: The Role of Connectivity, Rank, and Research ProductivityErica T Warner, René Carapinha, Griffin M Weber, et al.
Cancer|September 11, 2023
Breast cancer survivorship experiences among Black womenNaomi Y Ko, Tsion G Fikre, Anne K Buck, et al.
Parkinsonism & Related Disorders|April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystoniaJustus L Groen, Katja Ritz, Tom T Warner, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|April 23, 2010
Inhaled morphine for palliation of dyspnea in end-stage cystic fibrosisDon Hayes, Michael I Anstead, Rena T Warner, et al.
Infection and Immunity|December 1, 1996
Importance of beta2-microglobulin in murine resistance to mucosal and systemic candidiasisE Balish, F A Vazquez-Torres, J Jones-Carson, et al.
Urology|June 4, 1998
Laparoscopic cryosurgery of the kidney in the porcine model: an acute histological studyS Y Nakada, F T Lee, T Warner, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|April 9, 2015
Considering context in academic medicine: differences in demographic and professional characteristics and in research productivity and advancement metrics across seven clinical departmentsErica T Warner, René Carapinha, Griffin M Weber, et al.
Journal of the Neurological Sciences|November 11, 2003
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegiaP A Wilkinson, P E Hart, H Patel, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
Pageof 41

Showing results (111-120 of 403) with videos related to

Sort By:
Pageof 41
Journal of Women'S Health (2002)|March 31, 2017
Organizational Context and Female Faculty's Perception of the Climate for Women in Academic MedicineRené Carapinha, Caitlin M McCracken, Erica T Warner, et al.
Journal of Women'S Health (2002)|August 4, 2017
Gender Differences in Receipt of National Institutes of Health R01 Grants Among Junior Faculty at an Academic Medical Center: The Role of Connectivity, Rank, and Research ProductivityErica T Warner, René Carapinha, Griffin M Weber, et al.
Cancer|September 11, 2023
Breast cancer survivorship experiences among Black womenNaomi Y Ko, Tsion G Fikre, Anne K Buck, et al.
Parkinsonism & Related Disorders|April 29, 2014
DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystoniaJustus L Groen, Katja Ritz, Tom T Warner, et al.
American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists|April 23, 2010
Inhaled morphine for palliation of dyspnea in end-stage cystic fibrosisDon Hayes, Michael I Anstead, Rena T Warner, et al.
Infection and Immunity|December 1, 1996
Importance of beta2-microglobulin in murine resistance to mucosal and systemic candidiasisE Balish, F A Vazquez-Torres, J Jones-Carson, et al.
Urology|June 4, 1998
Laparoscopic cryosurgery of the kidney in the porcine model: an acute histological studyS Y Nakada, F T Lee, T Warner, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|April 9, 2015
Considering context in academic medicine: differences in demographic and professional characteristics and in research productivity and advancement metrics across seven clinical departmentsErica T Warner, René Carapinha, Griffin M Weber, et al.
Journal of the Neurological Sciences|November 11, 2003
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegiaP A Wilkinson, P E Hart, H Patel, et al.
Annals of Human Genetics|March 30, 2000
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutationsE M Valente, S Povey, T T Warner, et al.
Pageof 41