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Blood Cells, Molecules & Diseases|October 14, 2015
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi JewsMartin de Boer, Shay Tzur, Karin van Leeuwen, et al.
European Heart Journal|November 9, 2006
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?Nynke Hofman, Arthur A M Wilde, Stefan Kääb, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2006
Association of connective tissue growth factor with fibrosis in vitreoretinal disorders in the human eyeEsther J Kuiper, Marc D de Smet, Jan C van Meurs, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2009
Genetic polymorphisms in the DRD2, DRD3, and SLC6A3 gene in elderly patients with deliriumBarbara C van Munster, Mojgan Yazdanpanah, Michael W T Tanck, et al.
European Heart Journal|July 11, 2006
Diagnosing familial hypercholesterolaemia: the relevance of genetic testingEmily S van Aalst-Cohen, Angelique C M Jansen, Michael W T Tanck, et al.
BMJ Open Respiratory Research|August 8, 2023
In vivo polarisation sensitive optical coherence tomography for fibrosis assessment in interstitial lung disease: a prospective, exploratory, observational studyMargherita Vaselli, Kirsten Kalverda-Mooij, Erik Thunnissen, et al.
American Journal of Respiratory Cell and Molecular Biology|May 19, 2009
Priming of alveolar macrophages upon instillation of lipopolysaccharide in the human lungJacobien J Hoogerwerf, Alex F de Vos, Cornelis van't Veer, et al.
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