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M Ponder

Showing results (21-30 of 31) with videos related to

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Psychoneuroendocrinology|November 16, 2025
First-generation college student status and minoritized race and ethnicity: Intersectional predictors of life stress exposure and lab-based cortisol reactivityDarha M Ponder, Suzanne Vrshek-Schallhorn, Chelsea B Crayton, et al.
Journal of Community Psychology|July 14, 2026
Development of the ROOTS Intervention: A Culturally Relevant Parenting Program for Promoting the Emotional and Physical Health of Young ChildrenDaniel K Cooper, Francesca Lupini, Subina Saini, et al.
Clinical Ophthalmology (Auckland, N.Z.)|October 23, 2023
Timing of Jones Tube Placement After Excision of Nasal or Lacrimal Drainage System Malignancy: A Survey of the American Society of Ophthalmic Plastic and Reconstructive Surgery (ASOPRS)Tom Kornhauser, Christian M Ponder, Philip W Dockery, et al.
Studies in Health Technology and Informatics|March 8, 2005
JUST in time health emergency interventions: an innovative approach to training the citizen for emergency situations using virtual reality techniques and advanced IT tools (the VR Tool)A Manganas, M Tsiknakis, E Leisch, et al.
Journal of Cataract and Refractive Surgery|October 15, 2021
Intraoperative complications and visual outcomes of cataract surgery in patients with retinal vein occlusion: multicenter database studyChristian M Ponder, Peyton A Rather, Mohmed K Soliman, et al.
American Journal of Human Genetics|April 1, 1993
Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21S A Smith, D F Easton, D Ford, et al.
Human Molecular Genetics|April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A familiesR McMahon, L M Mulligan, C S Healey, et al.
Clinical Immunology (Orlando, Fla.)|October 3, 2022
IL-4 receptor blockade is a global repressor of naïve B cell development and responses in a dupilumab-treated patientJohn D Mountz, Min Gao, David M Ponder, et al.
Human Genetics|July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delayM Upadhyaya, M Ruggieri, J Maynard, et al.
American Journal of Human Genetics|January 1, 1989
Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type IC G Mathew, K Thorpe, D F Easton, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Psychoneuroendocrinology|November 16, 2025
First-generation college student status and minoritized race and ethnicity: Intersectional predictors of life stress exposure and lab-based cortisol reactivityDarha M Ponder, Suzanne Vrshek-Schallhorn, Chelsea B Crayton, et al.
Journal of Community Psychology|July 14, 2026
Development of the ROOTS Intervention: A Culturally Relevant Parenting Program for Promoting the Emotional and Physical Health of Young ChildrenDaniel K Cooper, Francesca Lupini, Subina Saini, et al.
Clinical Ophthalmology (Auckland, N.Z.)|October 23, 2023
Timing of Jones Tube Placement After Excision of Nasal or Lacrimal Drainage System Malignancy: A Survey of the American Society of Ophthalmic Plastic and Reconstructive Surgery (ASOPRS)Tom Kornhauser, Christian M Ponder, Philip W Dockery, et al.
Studies in Health Technology and Informatics|March 8, 2005
JUST in time health emergency interventions: an innovative approach to training the citizen for emergency situations using virtual reality techniques and advanced IT tools (the VR Tool)A Manganas, M Tsiknakis, E Leisch, et al.
Journal of Cataract and Refractive Surgery|October 15, 2021
Intraoperative complications and visual outcomes of cataract surgery in patients with retinal vein occlusion: multicenter database studyChristian M Ponder, Peyton A Rather, Mohmed K Soliman, et al.
American Journal of Human Genetics|April 1, 1993
Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21S A Smith, D F Easton, D Ford, et al.
Human Molecular Genetics|April 1, 1994
Direct, non-radioactive detection of mutations in multiple endocrine neoplasia type 2A familiesR McMahon, L M Mulligan, C S Healey, et al.
Clinical Immunology (Orlando, Fla.)|October 3, 2022
IL-4 receptor blockade is a global repressor of naïve B cell development and responses in a dupilumab-treated patientJohn D Mountz, Min Gao, David M Ponder, et al.
Human Genetics|July 8, 1998
Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delayM Upadhyaya, M Ruggieri, J Maynard, et al.
American Journal of Human Genetics|January 1, 1989
Linkage analysis of chromosome 17 markers in British and South African families with neurofibromatosis type IC G Mathew, K Thorpe, D F Easton, et al.
Pageof 4