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P Coucke

Showing results (101-110 of 157) with videos related to

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Human Genetics|January 1, 1993
Molecular study of chromosome 15 in 22 patients with Angelman syndromeJ Beuten, K Mangelschots, I Buntinx, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|July 17, 2022
[Feasibility study: The medical imaging as a tool for therapeutic education in radiotherapy]D Kirkove, N Barthelemy, P Coucke, et al.
Planta Medica|February 1, 1994
Effects of alpha-hederin, a saponin extracted from Hedera helix, on cells cultured in vitroS Danloy, J Quetin-Leclercq, P Coucke, et al.
Archives of Dermatological Research|January 1, 1993
An immunohistochemical and histochemical study of cytokeratin, involucrin and transglutaminase in seborrhoeic keratosisD Broekaert, I M Leigh, E B Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31----q32P Coucke, K Mangelschots, F Speleman, et al.
Revue Medicale De Liege|May 15, 2014
[Radiotherapy for elderly patient with rectal cancer: which benefit?]P Martinive, S Allepaert, D Vandaele, et al.
The Laryngoscope|January 31, 1998
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2H Kunst, H Marres, P Huygen, et al.
International Journal of Radiation Oncology, Biology, Physics|February 28, 2003
Reno, a European postmarket surveillance registry, confirms effectiveness of coronary brachytherapy in routine clinical practiceV Coen, P Serruys, W Sauerwein, et al.
Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Pageof 16

Showing results (101-110 of 157) with videos related to

Sort By:
Pageof 16
Human Genetics|January 1, 1993
Molecular study of chromosome 15 in 22 patients with Angelman syndromeJ Beuten, K Mangelschots, I Buntinx, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|July 17, 2022
[Feasibility study: The medical imaging as a tool for therapeutic education in radiotherapy]D Kirkove, N Barthelemy, P Coucke, et al.
Planta Medica|February 1, 1994
Effects of alpha-hederin, a saponin extracted from Hedera helix, on cells cultured in vitroS Danloy, J Quetin-Leclercq, P Coucke, et al.
Archives of Dermatological Research|January 1, 1993
An immunohistochemical and histochemical study of cytokeratin, involucrin and transglutaminase in seborrhoeic keratosisD Broekaert, I M Leigh, E B Lane, et al.
Cytogenetics and Cell Genetics|January 1, 1991
Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31----q32P Coucke, K Mangelschots, F Speleman, et al.
Revue Medicale De Liege|May 15, 2014
[Radiotherapy for elderly patient with rectal cancer: which benefit?]P Martinive, S Allepaert, D Vandaele, et al.
The Laryngoscope|January 31, 1998
Nonsyndromic autosomal dominant progressive sensorineural hearing loss: audiologic analysis of a pedigree linked to DFNA2H Kunst, H Marres, P Huygen, et al.
International Journal of Radiation Oncology, Biology, Physics|February 28, 2003
Reno, a European postmarket surveillance registry, confirms effectiveness of coronary brachytherapy in routine clinical practiceV Coen, P Serruys, W Sauerwein, et al.
Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Pageof 16