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Halley

Showing results (1131-1140 of 1,394) with videos related to

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Hospital Pediatrics|June 2, 2021
Physiologic Monitor Alarm Burden and Nurses' Subjective Workload in a Children's HospitalIrit R Rasooly, Andrew S Kern-Goldberger, Rui Xiao, et al.
The American Surgeon|May 3, 2013
Gastric electrical stimulation for abdominal pain in patients with symptoms of gastroparesisChristopher J Lahr, James Griffith, Charu Subramony, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 8, 2025
Human kallikrein 2: A novel lineage-specific surface target in prostate cancerFei Shen, Ryan Smith, Theresa McDevitt, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 23, 2013
Maternal folate depletion and high-fat feeding from weaning affects DNA methylation and DNA repair in brain of adult offspringSabine A S Langie, Sebastian Achterfeldt, Joanna P Gorniak, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.
Journal of Medical Primatology|July 5, 2020
SARS-CoV-2 surveillance for a non-human primate breeding research facilityJoAnn L Yee, Koen K A Van Rompay, Amanda B Carpenter, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2024
Plant, insect, and fungi fossils under the center of Greenland's ice sheet are evidence of ice-free timesPaul R Bierman, Halley M Mastro, Dorothy M Peteet, et al.
Comprehensive Psychiatry|June 9, 2023
Translation and Validation of the Gaming Disorder Test and Gaming Disorder Scale for Adolescents into Chinese for Taiwanese Young AdultsTzu-Yi Wu, Shih-Wei Huang, Jung-Sheng Chen, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Clinics (Sao Paulo, Brazil)|April 26, 2025
Novel variants of the ATRX gene identified in MYCN non-amplified Neuroblastoma in Brazilian patientsThamiris Magalhães Gimenez, Vanessa Pretes Peralta, Ricardo Rodrigues Giorgi, et al.
Pageof 140

Showing results (1131-1140 of 1,394) with videos related to

Sort By:
Pageof 140
Hospital Pediatrics|June 2, 2021
Physiologic Monitor Alarm Burden and Nurses' Subjective Workload in a Children's HospitalIrit R Rasooly, Andrew S Kern-Goldberger, Rui Xiao, et al.
The American Surgeon|May 3, 2013
Gastric electrical stimulation for abdominal pain in patients with symptoms of gastroparesisChristopher J Lahr, James Griffith, Charu Subramony, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 8, 2025
Human kallikrein 2: A novel lineage-specific surface target in prostate cancerFei Shen, Ryan Smith, Theresa McDevitt, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 23, 2013
Maternal folate depletion and high-fat feeding from weaning affects DNA methylation and DNA repair in brain of adult offspringSabine A S Langie, Sebastian Achterfeldt, Joanna P Gorniak, et al.
Human Reproduction (Oxford, England)|January 5, 2002
Genetic risk factors in infertile men with severe oligozoospermia and azoospermiaG R Dohle, D J J Halley, J O Van Hemel, et al.
Journal of Medical Primatology|July 5, 2020
SARS-CoV-2 surveillance for a non-human primate breeding research facilityJoAnn L Yee, Koen K A Van Rompay, Amanda B Carpenter, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 2024
Plant, insect, and fungi fossils under the center of Greenland's ice sheet are evidence of ice-free timesPaul R Bierman, Halley M Mastro, Dorothy M Peteet, et al.
Comprehensive Psychiatry|June 9, 2023
Translation and Validation of the Gaming Disorder Test and Gaming Disorder Scale for Adolescents into Chinese for Taiwanese Young AdultsTzu-Yi Wu, Shih-Wei Huang, Jung-Sheng Chen, et al.
Journal of Medical Genetics|December 10, 1997
Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locusM Losekoot, E Hoogendoorn, R Olmer, et al.
Clinics (Sao Paulo, Brazil)|April 26, 2025
Novel variants of the ATRX gene identified in MYCN non-amplified Neuroblastoma in Brazilian patientsThamiris Magalhães Gimenez, Vanessa Pretes Peralta, Ricardo Rodrigues Giorgi, et al.
Pageof 140