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Eric Pasmant

Showing results (111-120 of 124) with videos related to

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Endocrine Pathology|March 19, 2026
Clinical and Pathological Features of EC-cell Familial Small Intestine Neuroendocrine Tumors: A Nationwide Cohort From the French GTE-RENATEN NetworkThomas Hunaut, Laura Gérard, Agathe Hercent, et al.
Journal of Medical Genetics|June 19, 2016
<i>SETD2</i> and <i>DNMT3A</i> screen in the Sotos-like syndrome French cohortCamille Tlemsani, Armelle Luscan, Nicolas Leulliot, et al.
European Journal of Human Genetics : EJHG|December 13, 2021
Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal studyClaire Forde, Emma Burkitt-Wright, Peter D Turnpenny, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
2016 Children's Tumor Foundation conference on neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosisMichael J Fisher, Allan J Belzberg, Peter de Blank, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
KDM1A inactivation causes hereditary food-dependent Cushing syndromeAnna Vaczlavik, Lucas Bouys, Florian Violon, et al.
European Journal of Endocrinology|February 8, 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlationLucas Bouys, Patricia Vaduva, Anne Jouinot, et al.
Nature Communications|October 6, 2025
Impact of steroid differentiation on tumor microenvironment revealed by single-nucleus atlas of adrenal tumorsAnne Jouinot, Yoann Martin, Florian Violon, et al.
European Journal of Endocrinology|May 6, 2022
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patientsLucas Bouys, Anna Vaczlavik, Anne Jouinot, et al.
Leukemia|March 31, 2022
RAS activation induces synthetic lethality of MEK inhibition with mitochondrial oxidative metabolism in acute myeloid leukemiaJustine Decroocq, Rudy Birsen, Camille Montersino, et al.
Cancers|July 2, 2021
Severe Phenotype in Patients with Large Deletions of <i>NF1</i>Laurence Pacot, Dominique Vidaud, Audrey Sabbagh, et al.
Pageof 13

Showing results (111-120 of 124) with videos related to

Sort By:
Pageof 13
Endocrine Pathology|March 19, 2026
Clinical and Pathological Features of EC-cell Familial Small Intestine Neuroendocrine Tumors: A Nationwide Cohort From the French GTE-RENATEN NetworkThomas Hunaut, Laura Gérard, Agathe Hercent, et al.
Journal of Medical Genetics|June 19, 2016
<i>SETD2</i> and <i>DNMT3A</i> screen in the Sotos-like syndrome French cohortCamille Tlemsani, Armelle Luscan, Nicolas Leulliot, et al.
European Journal of Human Genetics : EJHG|December 13, 2021
Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal studyClaire Forde, Emma Burkitt-Wright, Peter D Turnpenny, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
2016 Children's Tumor Foundation conference on neurofibromatosis type 1, neurofibromatosis type 2, and schwannomatosisMichael J Fisher, Allan J Belzberg, Peter de Blank, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
KDM1A inactivation causes hereditary food-dependent Cushing syndromeAnna Vaczlavik, Lucas Bouys, Florian Violon, et al.
European Journal of Endocrinology|February 8, 2025
KDM1A genetic alterations, a rare cause of primary bilateral macronodular adrenal hyperplasia, strongly associated with food-dependent Cushing's syndrome: results of its systematic germline screening in 301 index cases and genotype/phenotype correlationLucas Bouys, Patricia Vaduva, Anne Jouinot, et al.
Nature Communications|October 6, 2025
Impact of steroid differentiation on tumor microenvironment revealed by single-nucleus atlas of adrenal tumorsAnne Jouinot, Yoann Martin, Florian Violon, et al.
European Journal of Endocrinology|May 6, 2022
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene ARMC5 in 352 unselected patientsLucas Bouys, Anna Vaczlavik, Anne Jouinot, et al.
Leukemia|March 31, 2022
RAS activation induces synthetic lethality of MEK inhibition with mitochondrial oxidative metabolism in acute myeloid leukemiaJustine Decroocq, Rudy Birsen, Camille Montersino, et al.
Cancers|July 2, 2021
Severe Phenotype in Patients with Large Deletions of <i>NF1</i>Laurence Pacot, Dominique Vidaud, Audrey Sabbagh, et al.
Pageof 13