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D Lacombe

Showing results (141-150 of 225) with videos related to

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European Journal of Cancer (Oxford, England : 1990)|June 5, 2004
RFS2000 (9-nitrocamptothecin) in advanced small cell lung cancer, a phase II study of the EORTC New Drug Development GroupC J A Punt, M J A de Jonge, S Monfardini, et al.
European Journal of Cancer (Oxford, England : 1990)|February 5, 2003
Phase II study of XR 5000 (DACA), an inhibitor of topoisomerase I and II, administered as a 120-h infusion in patients with non-small cell lung cancerC Dittrich, B Coudert, L Paz-Ares, et al.
The Journal of Investigative Dermatology|July 1, 1995
The gene for Bazex-Dupré-Christol syndrome maps to chromosome XqP Vabres, D Lacombe, L G Rabinowitz, et al.
JACC. Case Reports|September 20, 2022
Complex Management Decisions in a Professional Athlete With Recurrent PericarditisBenjamin M Klein, Eunice S Dugan, Andrew D LaCombe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 6, 2005
[Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition?]S Meyer Witte, C Espil-Taris, C Cenraud, et al.
American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 1, 2009
EORTC Elderly Task Force and Lung Cancer Group and International Society for Geriatric Oncology (SIOG) experts' opinion for the treatment of non-small-cell lung cancer in an elderly populationA G Pallis, C Gridelli, J P van Meerbeeck, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|April 13, 2006
[Genetics and orthopedics: genetic implications of congenital limb abnormalities]M Holder-Espinasse, B Herbaux, A Mezel, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
European Journal of Medical Genetics|October 8, 2009
Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imagingM J Alao, D Bonneau, M Holder-Espinasse, et al.
Pageof 23

Showing results (141-150 of 225) with videos related to

Sort By:
Pageof 23
European Journal of Cancer (Oxford, England : 1990)|June 5, 2004
RFS2000 (9-nitrocamptothecin) in advanced small cell lung cancer, a phase II study of the EORTC New Drug Development GroupC J A Punt, M J A de Jonge, S Monfardini, et al.
European Journal of Cancer (Oxford, England : 1990)|February 5, 2003
Phase II study of XR 5000 (DACA), an inhibitor of topoisomerase I and II, administered as a 120-h infusion in patients with non-small cell lung cancerC Dittrich, B Coudert, L Paz-Ares, et al.
The Journal of Investigative Dermatology|July 1, 1995
The gene for Bazex-Dupré-Christol syndrome maps to chromosome XqP Vabres, D Lacombe, L G Rabinowitz, et al.
JACC. Case Reports|September 20, 2022
Complex Management Decisions in a Professional Athlete With Recurrent PericarditisBenjamin M Klein, Eunice S Dugan, Andrew D LaCombe, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 6, 2005
[Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition?]S Meyer Witte, C Espil-Taris, C Cenraud, et al.
American Journal of Medical Genetics|July 1, 1993
No evidence for linkage to the type 1 or type 2 neurofibromatosis loci in Noonan syndrome familiesW F Flintoff, M Bahuau, S Lyonnet, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 1, 2009
EORTC Elderly Task Force and Lung Cancer Group and International Society for Geriatric Oncology (SIOG) experts' opinion for the treatment of non-small-cell lung cancer in an elderly populationA G Pallis, C Gridelli, J P van Meerbeeck, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|April 13, 2006
[Genetics and orthopedics: genetic implications of congenital limb abnormalities]M Holder-Espinasse, B Herbaux, A Mezel, et al.
Human Molecular Genetics|October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR geneC Vincent, V Kalatzis, S Compain, et al.
European Journal of Medical Genetics|October 8, 2009
Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imagingM J Alao, D Bonneau, M Holder-Espinasse, et al.
Pageof 23