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Photodermatology, Photoimmunology & Photomedicine|February 1, 1991
Sunscreens with low sun protection factor inhibit ultraviolet B and A photoaging in the skin of the hairless albino mouseJ A Harrison, S L Walker, S R Plastow, et al.Gynecologic Oncology|February 1, 1994
Open interstitial brachytherapy for the treatment of local-regional recurrences of uterine corpus and cervix cancer after primary surgeryB J Monk, J L Walker, K Tewari, et al.Journal of the National Cancer Institute|January 1, 1977
Modification of hydroxyindole-O-methyltransferase activity in experimental pineocytomas induced in hamsters by a human papovavirus (JC)W B Quay, Y H Ma, J N Varakis, et al.Cancer|January 15, 1994
Prognostic utility of epidermal growth factor receptor overexpression in endometrial adenocarcinomaM A Khalifa, A A Abdoh, R S Mannel, et al.Gynecologic Oncology|June 1, 1997
Epidermal growth factor receptor in vulvar malignancies and its relationship to metastasis and patient survivalG A Johnson, R Mannel, M Khalifa, et al.Human Reproduction (Oxford, England)|November 1, 1990
Comparison of concurrent pregnancy rates for in-vitro fertilization--embryo transfer, pronuclear stage embryo transfer and gamete intra-fallopian transferD G Hammitt, C H Syrop, S J Hahn, et al.The Journal of Investigative Dermatology|April 8, 2006
Photoadaptation during narrowband ultraviolet-B therapy is independent of skin type: a study of 352 patientsRoy A Palmer, Susan Aquilina, Peter J Milligan, et al.Pharmacotherapy|March 13, 2019
The Association Between Central Nervous System-Active Medication Use and Fall-Related Injury in Community-Dwelling Older Adults with DementiaLaura A Hart, Zachary A Marcum, Shelly L Gray, et al.Cytogenetics and Cell Genetics|January 1, 1995
Colocalization of the rat homolog of the von Hippel Lindau (Vhl) gene and the plasma membrane Ca++ transporting ATPase isoform 2 (Atp2b2) gene to rat chromosome bands 4q41.3-->42.1C M Aldaz, R S Yeung, F Latif, et al.American Journal of Medical Genetics|August 1, 1982
Spinal dysraphia as an autosomal dominant defect in four familiesR M Fineman, L B Jorde, R A Martin, et al.Pageof 289