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Wim Wuyts

Showing results (11-20 of 135) with videos related to

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European Journal of Human Genetics : EJHG|May 30, 2003
Clinical and molecular analysis of nine families with Adams-Oliver syndromePieter Verdyck, Muriel Holder-Espinasse, Wim Van Hul, et al.
Archives of Iranian Medicine|April 23, 2008
Vitamin D-dependent rickets type II: report of a novel mutation in the vitamin D receptor geneYousef Shafeghati, Nima Momenin, Taher Esfahani, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
A subterminal deletion of the long arm of chromosome 10: a clinical report and reviewWinnie Courtens, Wim Wuyts, Liesbeth Rooms, et al.
European Heart Journal. Case Reports|October 30, 2019
Natural evolution of cardiac sarcoidosis in an asymptomatic patient: a case reportGanna Degtiarova, Olivier Gheysens, Johan Van Cleemput, et al.
Diabetes/Metabolism Research and Reviews|May 20, 2021
ABCC8 variants in MODY12: Review of the literature and report of a case with severe complicationsMarijke Timmers, Eveline Dirinck, Patrick Lauwers, et al.
Journal of Crohn'S & Colitis|September 4, 2016
Sarcoidosis-Like Lesions: Another Paradoxical Reaction to Anti-TNF Therapy?Amelie Decock, Gert Van Assche, Séverine Vermeire, et al.
BMC Bioinformatics|January 7, 2011
CNV-WebStore: online CNV analysis, storage and interpretationGeert Vandeweyer, Edwin Reyniers, Wim Wuyts, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|June 2, 2020
Connective tissue disease associated interstitial pneumonia: a challenge for both rheumatologists and pulmonologistsSarah Geerts, Wim Wuyts, Ellen De Langhe, et al.
Acta Clinica Belgica|May 18, 2021
Clinical characteristics of sarcoidosis patients in BelgiumJolien De Ridder, Steven Ronsmans, Steven Vanderschueren, et al.
Archivos Argentinos De Pediatria|November 22, 2016
Trichorhinophalangeal syndrome type II presenting with short stature in a childFiliz Hazan, Hüseyin A Korkmaz, Kanay Yararbaş, et al.
Pageof 14

Showing results (11-20 of 135) with videos related to

Sort By:
Pageof 14
European Journal of Human Genetics : EJHG|May 30, 2003
Clinical and molecular analysis of nine families with Adams-Oliver syndromePieter Verdyck, Muriel Holder-Espinasse, Wim Van Hul, et al.
Archives of Iranian Medicine|April 23, 2008
Vitamin D-dependent rickets type II: report of a novel mutation in the vitamin D receptor geneYousef Shafeghati, Nima Momenin, Taher Esfahani, et al.
American Journal of Medical Genetics. Part A|January 19, 2006
A subterminal deletion of the long arm of chromosome 10: a clinical report and reviewWinnie Courtens, Wim Wuyts, Liesbeth Rooms, et al.
European Heart Journal. Case Reports|October 30, 2019
Natural evolution of cardiac sarcoidosis in an asymptomatic patient: a case reportGanna Degtiarova, Olivier Gheysens, Johan Van Cleemput, et al.
Diabetes/Metabolism Research and Reviews|May 20, 2021
ABCC8 variants in MODY12: Review of the literature and report of a case with severe complicationsMarijke Timmers, Eveline Dirinck, Patrick Lauwers, et al.
Journal of Crohn'S & Colitis|September 4, 2016
Sarcoidosis-Like Lesions: Another Paradoxical Reaction to Anti-TNF Therapy?Amelie Decock, Gert Van Assche, Séverine Vermeire, et al.
BMC Bioinformatics|January 7, 2011
CNV-WebStore: online CNV analysis, storage and interpretationGeert Vandeweyer, Edwin Reyniers, Wim Wuyts, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|June 2, 2020
Connective tissue disease associated interstitial pneumonia: a challenge for both rheumatologists and pulmonologistsSarah Geerts, Wim Wuyts, Ellen De Langhe, et al.
Acta Clinica Belgica|May 18, 2021
Clinical characteristics of sarcoidosis patients in BelgiumJolien De Ridder, Steven Ronsmans, Steven Vanderschueren, et al.
Archivos Argentinos De Pediatria|November 22, 2016
Trichorhinophalangeal syndrome type II presenting with short stature in a childFiliz Hazan, Hüseyin A Korkmaz, Kanay Yararbaş, et al.
Pageof 14