Showing results (91-100 of 144) with videos related to

Sort By:
Pageof 15
Menopause International|September 6, 2007
Risk factors for clinical fractures among postmenopausal women: a 10-year prospective studyTineke A C M van Geel, Piet P Geusens, Ivo F Nagtzaam, et al.
Pharmacoepidemiology and Drug Safety|June 13, 2023
Comparison of characteristics of patients with lung cancer in U.K. primary care databases: Clinical Practice Research Datalink Aurum and GOLDJ L Gulikers, A J van Veelen, J H M Driessen, et al.
Bioanalysis|April 1, 2015
Improved pharmacodynamic assay for dihydropyrimidine dehydrogenase activity in peripheral blood mononuclear cellsDick Pluim, Bart A W Jacobs, Maarten J Deenen, et al.
Pediatrics|April 2, 2009
Long-term health and quality-of-life consequences of mass screening for childhood celiac disease: a 10-year follow-up studyEllen J van Koppen, Joachim J Schweizer, Cassandra G D S Csizmadia, et al.
The British Journal of Dermatology|October 9, 2012
Keratolysis exfoliativa (dyshidrosis lamellosa sicca): a distinct peeling entityY Y Chang, J van der Velden, G van der Wier, et al.
The British Journal of Dermatology|August 2, 2008
A newly identified splice site mutation in ZMPSTE24 causes restrictive dermopathy in the Middle EastC S Sander, N Salman, M van Geel, et al.
Plos One|June 2, 2018
Reduced mortality and subsequent fracture risk associated with oral bisphosphonate recommendation in a fracture liaison service setting: A prospective cohort studyTineke A C M van Geel, Dana Bliuc, Piet P M Geusens, et al.
The British Journal of Dermatology|December 7, 2018
Genetic profiling of basal cell carcinomas detects postzygotic mosaicism in basal cell naevus syndromeM G H C Reinders, B Cosgun, L M C Gijezen, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification of a novel beta-tubulin subfamily with one member (TUBB4Q) located near the telomere of chromosome region 4q35M van Geel, J C van Deutekom, A van Staalduinen, et al.
The British Journal of Dermatology|September 14, 2011
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryA M van Tuyll van Serooskerken, B I Drögemöller, K Te Velde, et al.
Pageof 15