Showing results (371-380 of 380) with videos related to

Sort By:
Pageof 38
You have reached the last page of results.This site can display upto 380 results.
Virchows Archiv : an International Journal of Pathology|February 8, 2019
National multicentric evaluation of quality of pathology reports for rectal cancer in France in 2016C Boutanos, M Capdepont, M Svrcek, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 2020
Abnormal morphology biases hematocrit distribution in tumor vasculature and contributes to heterogeneity in tissue oxygenationMiguel O Bernabeu, Jakub Köry, James A Grogan, et al.
Contemporary Clinical Trials|April 25, 2006
Rationale and design of the TRANSFACT project phase I: a study to assess the effect of the two different dietary sources of trans fatty acids on cardiovascular risk factors in humansJean-Michel Chardigny, Corinne Malpuech-Brugère, Fabiola Dionisi, et al.
BMC Medical Genetics|December 20, 2014
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficienciesThierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, et al.
Biomaterials Science|October 14, 2021
A tripartite carbohydrate-binding module to functionalize cellulose nanocrystalsAngeline Pelus, Gaëlle Bordes, Sophie Barbe, et al.
European Journal of Endocrinology|January 17, 2013
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysisThomas Cuny, Morgane Pertuit, Mona Sahnoun-Fathallah, et al.
Annales D'Endocrinologie|April 7, 2004
[Therapeutic strategies in somatotroph adenomas with extrasellar extension: role of the medical approach, a consensus study of the French Acromegaly Registry]Ph Jaquet, Ch Cortet-Rudelli, G Sassolas, et al.
The Journal of Clinical Endocrinology and Metabolism|December 23, 2004
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutationsSophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino, et al.
Endocrine-Related Cancer|February 1, 2012
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindredsMaria A Tichomirowa, Misu Lee, Anne Barlier, et al.
The Journal of Frailty & Aging|November 25, 2016
MACVIA-LR (Fighting Chronic Diseases for Active and Healthy Ageing in Languedoc-Roussillon): A Success Story of the European Innovation Partnership on Active and Healthy AgeingJ Bousquet, R Bourret, T Camuzat, et al.
Pageof 38