Costinetti, F. et al. 2019 2018 Consensus of the French Society of Endocrinology: endocrine toxicities of cancer immunotherapies Immunotherapy induced side effects: Are frequent, usually well-tolerated, and can lead to thyroid, pituitary, and less frequently adrenals and pancreas (fulminant diabetes) disease,. Do not... - issue: 2 - volume: 23 - pages: 31-36.
van Eif, VW. W. et al. 2019 Gradual differentiation and confinement of the cardiac conduction system as indicated by marker gene expression The components of the cardiac conduction system, responsible for coordinated activation of the heart chambers, are well defined and their cells differ in gene expression profile and phenotype from... Biochim Biophys Acta Mol Cell Res - issue: 3 - volume: 1867 - pages: 118509.
Payan, S. et al. 2019 Cardiomyocyte proliferation, a target for cardiac regeneration Cardiac diseases, characterized by cardiomyocyte loss, lead to dramatic impairment of cardiac function and ultimately to congestive heart failure. Despite significant advances, conventional treatments... Biochim Biophys Acta Mol Cell Res - issue: - volume: - pages: .
Mattei, J. et al. 2019 Distal extremities soft tissue sarcomas: Are they so different from other limb localizations? - issue: 4 - volume: 119 - pages: 479-488.
Mattei, J. et al. 2019 Distal extremities soft tissue sarcomas: Are they so different from other limb localizations? Background and Objectives Soft tissue sarcoma localization in distal extremities (DESTS) of the limbs (hand/fingers, and foot/toes) is unusual. The literature is scarce about their behavior and this... - issue: 4 - volume: 119 - pages: 479-488.
Etchevers, HC. et al. 2019 The diverse neural crest: from embryology to human pathology We review here some of the historical highlights in exploratory studies of the vertebrate embryonic structure known as the neural crest. The study of the molecular properties of the cells that it... Development - issue: - volume: 146(5) - pages: dev.169821.
Romanet, P. et al. 2019 UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population Context: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disease caused by mutations in the MEN1 gene characterized by a broad spectrum of clinical manifestations, of which the... - issue: 3 - volume: 104 - pages: 753-764.
Etchevers, HC. et al. 2019 The diverse neural crest: from embryology to human pathology We review here some of the historical highlights in exploratory studies of the vertebrate embryonic structure known as the neural crest. The study of the molecular properties of the cells that it... - issue: - volume: - pages: .
Brue, T. et al. 2019 Diabetes in patients with acromegaly treated with pegvisomant: observations from acrostudy PurposeTo explore the effects of pegvisomant (PEGV) on glucose metabolism in patients with acromegaly within ACROSTUDY, an international, observational, prospective safety surveillance... - issue: 3 - volume: 63 - pages: 563-572.
Valence, S. et al. 2019 Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies Purpose: To investigate the genetic basis of congenital ataxias (CAs), a unique group of cerebellar ataxias with a nonprogressive course, in 20 patients from consanguineous families, and to identify... - issue: 3 - volume: 21 - pages: 553-563.
Krahn, M. et al. 2019 A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing Next-generation sequencing (NGS) gene-panel-based analyses constitute diagnosis strategies which are adapted to the genetic heterogeneity within the field of myopathies, including more than 200... - issue: 3 - volume: 27 - pages: 349-352.
Tsuge, Y. et al. 2019 Enhanced production of d-lactate from mixed sugars in Corynebacterium glutamicum by overexpression of glycolytic genes encoding phosphofructokinase and triosephosphate isomerase The use of mixed sugars containing glucose and xylose in lignocellulosic biomass is desirable for the microbial production of chemicals and fuels. We investigated the effect of individual or... J. Biosci. Bioeng. - issue: 3 - volume: 127 - pages: 288-293.
Milleron, O. et al. 2019 Clinical Significance of Aortic Root Modification Associated With Bicuspid Aortic Valve in Marfan Syndrome An Observational Cohort Study - issue: 3 - volume: 12 - pages: .
de Nonneville, A. et al. 2019 Validation of Neutrophil Count as An Algorithm-Based Predictive Factor of Progression-Free Survival in Patients with Metastatic Soft Tissue Sarcomas Treated with Trabectedin - issue: 3 - volume: 11 - pages: .
Romanet, P. et al. 2019 UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population - issue: 3 - volume: 104 - pages: 753-764.
Etchevers, HC. et al. 2019 The diverse neural crest: from embryology to human pathology - issue: 5 - volume: 146 - pages: .
Brue, T. et al. 2019 Diabetes in patients with acromegaly treated with pegvisomant: observations from acrostudy - issue: 3 - volume: 63 - pages: 563-572.
Valence, S. et al. 2019 Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies - issue: 3 - volume: 21 - pages: 553-563.
Krahn, M. et al. 2019 A National French consensus on gene lists for the diagnosis of myopathies using next-generation sequencing - issue: 3 - volume: 27 - pages: 349-352.
Castinetti, F. et al. 2019 Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study. BACKGROUND: Multiple endocrine neoplasia type 2B is a rare syndrome caused mainly by Met918Thr germline RET mutation, and characterised by medullary thyroid carcinoma, phaeochromocytoma, and... Lancet Diabetes Endocrinol - issue: 3 - volume: 7 - pages: 213-220.