Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Boute

Showing results (151-160 of 232) with videos related to

Pageof 24
Sort By:
European Heart Journal. Cardiovascular Imaging|November 17, 2025
Lipoprotein(a) and long-term structural valve degeneration of aortic bioprosthesesMarin Boute, Paul Salembier, Anne-Catherine Pouleur, et al.
Molecular Cancer Therapeutics|October 10, 2019
Efficacy of the Antibody-Drug Conjugate W0101 in Preclinical Models of IGF-1 Receptor Overexpressing Solid TumorsBarbara Akla, Matthieu Broussas, Noureddine Loukili, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Cancer Therapeutics|June 15, 2016
A New Anti-CXCR4 Antibody That Blocks the CXCR4/SDF-1 Axis and Mobilizes Effector CellsMatthieu Broussas, Nicolas Boute, Barbara Akla, et al.
Scientific Reports|October 3, 2020
Crawl positioning improves set-up precision and patient comfort in prone whole breast irradiationPieter Deseyne, Bruno Speleers, Wilfried De Neve, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.
JACC. Advances|June 28, 2024
Quantifying the Survival Loss Linked to Late Therapeutic Indication in High-Gradient Severe Aortic StenosisDavid De Azevedo, Marin Boute, Christophe Tribouilloy, et al.
Clinical Genetics|July 2, 2021
The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndromeLeïla Ghesh, Marie Denis Musquer, Louise Devisme, et al.
European Journal of Medical Genetics|September 1, 2022
TRIT1 deficiency: Two novel patients with four novel variantsThomas Smol, Perrine Brunelle, Roseline Caumes, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
Pageof 24

Showing results (151-160 of 232) with videos related to

Sort By:
Pageof 24
European Heart Journal. Cardiovascular Imaging|November 17, 2025
Lipoprotein(a) and long-term structural valve degeneration of aortic bioprosthesesMarin Boute, Paul Salembier, Anne-Catherine Pouleur, et al.
Molecular Cancer Therapeutics|October 10, 2019
Efficacy of the Antibody-Drug Conjugate W0101 in Preclinical Models of IGF-1 Receptor Overexpressing Solid TumorsBarbara Akla, Matthieu Broussas, Noureddine Loukili, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Cancer Therapeutics|June 15, 2016
A New Anti-CXCR4 Antibody That Blocks the CXCR4/SDF-1 Axis and Mobilizes Effector CellsMatthieu Broussas, Nicolas Boute, Barbara Akla, et al.
Scientific Reports|October 3, 2020
Crawl positioning improves set-up precision and patient comfort in prone whole breast irradiationPieter Deseyne, Bruno Speleers, Wilfried De Neve, et al.
American Journal of Medical Genetics. Part A|May 17, 2007
The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritanceDavid Chitayat, Hana Sroka, Sarah Keating, et al.
JACC. Advances|June 28, 2024
Quantifying the Survival Loss Linked to Late Therapeutic Indication in High-Gradient Severe Aortic StenosisDavid De Azevedo, Marin Boute, Christophe Tribouilloy, et al.
Clinical Genetics|July 2, 2021
The first two non-Finnish HYLS1 variants: Expanding the phenotypic spectrum of hydrolethalus syndromeLeïla Ghesh, Marie Denis Musquer, Louise Devisme, et al.
European Journal of Medical Genetics|September 1, 2022
TRIT1 deficiency: Two novel patients with four novel variantsThomas Smol, Perrine Brunelle, Roseline Caumes, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
Pageof 24