Results 141 to 150 of about 52,728 (165)

First‐trimester nuchal abnormalities secondary to dehydrated hereditary stomatocytosis

Prenatal Diagnosis, 2009
O. Ami, O. Picone, L. Garçon, C. Castel, C. Guitton, J. Delaunay, R. Frydman, M. Senat   +7 more
semanticscholar   +1 more source

Prevalence of Attention Deficit Hyperactivity Disorder (ADHD) among Substance Use Disorder (SUD) Populations: Meta-Analysis

International Journal of Environmental Research and Public Health, 2023
Nikolas Gaspar
exaly  

SARS-CoV-2 Nsp3 unique domain SUD interacts with guanine quadruplexes and G4-ligands inhibit this interaction

Nucleic Acids Research, 2021
Marc Lavigne, Bruno Baron, Sébastien Brûlé   +2 more
exaly  

Correlation between ultrasound and pathological examination in a prenatal diagnosis of Cri du Chat syndrome associated with partial trisomy 17q

Prenatal Diagnosis, 2008
A. Cordier, C. Braidy, J. Levaillant, S. Brisset, M. Maurin, A. E. Mas, René Frydman, G. Tachdjian, Olivier Picone   +8 more
semanticscholar   +1 more source

Trust and collaboration between patients and staff in SUD treatment: A qualitative study of patients’ reflections on inpatient SUD treatment four years after discharge

NAD Nordic Studies on Alcohol and Drugs, 2022
Turid Wangensteen, Jacob Hystad
exaly  

Interstitial deletion 6p22.3‐p24.3 characterized by CGH array in a foetus with multiple malformations

Prenatal Diagnosis, 2009
Claire Colmant, Claire Colmant, S. Brisset, S. Brisset, G. Tachdjian, G. Tachdjian, Valérie Gautier, M. Ftouki, M. Laroudie, L. Druart, René Frydman, René Frydman, Olivier Picone, Olivier Picone   +13 more
semanticscholar   +1 more source

Adverse childhood experiences (ACEs) and substance use disorder (SUD): A scoping review

Drug and Alcohol Dependence, 2021
Leire Leza, Sandra Siria, José Javier López-Goñi   +2 more
exaly  

État des lieux après inclusion de 162 patients dans le PHRC national Y-BLOC21 « évaluation de la sexualité et de la fertilité des hommes nés avec une forme classique de déficit en 21 hydroxylase »

, 2012
L. Esterle, V. Tardy, P. Renoult-Pierre, S. Christin-Maitre, V. Kerlan, J. Bertherat, J. Kuhn, P. Caron, O. Chabre, D. Dewailly, P. Touraine, J. Young, C. Bouvattier   +12 more
semanticscholar   +1 more source

La mutation p.Arg31Cys de GNRH1 est responsable d’une forme autosomique dominante d’hypogonadisme hypogonadotrope par un effet dominant négatif

, 2012
L. Maione, P. Bouchard, F. Albarel, Régis Bobe, R. Pivonello, A. Colao, T. Brue, R. P. Millar, M. Lombès, J. Young, A. Guiochon-Mantel, J. Bouligand   +11 more
semanticscholar   +1 more source

SARS Unique Domain (SUD) of Severe Acute Respiratory Syndrome Coronavirus Induces NLRP3 Inflammasome-Dependent CXCL10-Mediated Pulmonary Inflammation

International Journal of Molecular Sciences, 2020
Hsin-Hou Chang, Su-Hua Huang, Cheng-Wen Lin   +2 more
exaly