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G van Camp

Showing results (111-120 of 214) with videos related to

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European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 27, 2022
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresiaJ Mortier, J van den Ende, F Declau, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA 2, 5, 8, 12G Van Camp, P J Coucke, P Van Hauwe, et al.
Ultrasound in Medicine & Biology|October 7, 2008
Influence of heart rate reduction on Doppler myocardial imaging parameters in a small animal modelC Weytjens, J D'hooge, S Droogmans, et al.
Genomics|November 5, 1997
Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11K Kastury, W E Taylor, M Gutierrez, et al.
American Journal of Human Genetics|October 23, 1997
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6pM R Brown, M S Tomek, L Van Laer, et al.
European Journal of Cancer & Clinical Oncology|September 1, 1986
Recombinant interferon alfa-2C versus polychemotherapy (VMCP) for treatment of multiple myeloma: a prospective randomized trialH Ludwig, A Cortelezzi, W Scheithauer, et al.
The Anatomical Record|May 23, 2000
High resolution imaging of the mouse inner ear by microtomography: a new tool in inner ear researchM P Van Spaendonck, K Cryns, P H Van De Heyning, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 10, 1998
Quantification of mitral regurgitation by the automated cardiac output method: an in vitro and in vivo studyG Van Camp, S Carlier, B Cosyns, et al.
Clinical Otolaryngology and Allied Sciences|February 15, 2002
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyW I Verhagen, S J Bom, E Fransen, et al.
Thorax|May 1, 1997
Superior vena cava syndrome associated with Nocardia farcinica infectionS Abdelkafi, D Dubail, T Bosschaerts, et al.
Pageof 22

Showing results (111-120 of 214) with videos related to

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Pageof 22
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 27, 2022
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresiaJ Mortier, J van den Ende, F Declau, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA 2, 5, 8, 12G Van Camp, P J Coucke, P Van Hauwe, et al.
Ultrasound in Medicine & Biology|October 7, 2008
Influence of heart rate reduction on Doppler myocardial imaging parameters in a small animal modelC Weytjens, J D'hooge, S Droogmans, et al.
Genomics|November 5, 1997
Chromosomal mapping of two members of the human dynein gene family to chromosome regions 7p15 and 11q13 near the deafness loci DFNA 5 and DFNA 11K Kastury, W E Taylor, M Gutierrez, et al.
American Journal of Human Genetics|October 23, 1997
A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6pM R Brown, M S Tomek, L Van Laer, et al.
European Journal of Cancer & Clinical Oncology|September 1, 1986
Recombinant interferon alfa-2C versus polychemotherapy (VMCP) for treatment of multiple myeloma: a prospective randomized trialH Ludwig, A Cortelezzi, W Scheithauer, et al.
The Anatomical Record|May 23, 2000
High resolution imaging of the mouse inner ear by microtomography: a new tool in inner ear researchM P Van Spaendonck, K Cryns, P H Van De Heyning, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|July 10, 1998
Quantification of mitral regurgitation by the automated cardiac output method: an in vitro and in vivo studyG Van Camp, S Carlier, B Cosyns, et al.
Clinical Otolaryngology and Allied Sciences|February 15, 2002
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyW I Verhagen, S J Bom, E Fransen, et al.
Thorax|May 1, 1997
Superior vena cava syndrome associated with Nocardia farcinica infectionS Abdelkafi, D Dubail, T Bosschaerts, et al.
Pageof 22