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Psychopharmacology|November 16, 2013
Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug developmentAndreea S Pop, Baltazar Gomez-Mancilla, Giovanni Neri, et al.
Nanomaterials (Basel, Switzerland)|March 29, 2017
CO and NO₂ Selective Monitoring by ZnO-Based SensorsMokhtar Hjiri, Lassaad El Mir, Salvatore Gianluca Leonardi, et al.
Nanomaterials (Basel, Switzerland)|November 27, 2021
Electrochemical and Fluorescent Properties of Crown Ether Functionalized Graphene Quantum Dots for Potassium and Sodium Ions DetectionDaniela Iannazzo, Claudia Espro, Angelo Ferlazzo, et al.
Sensors (Basel, Switzerland)|March 6, 2021
Fabrication of a Novel Electrochemical Sensor Based on Carbon Cloth Matrix Functionalized with MoO3 and 2D-MoS2 Layers for Riboflavin DeterminationRayhane Zribi, Antonino Foti, Maria Grazia Donato, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutationMarie A Shaw, Pietro Chiurazzi, Dennis R Romain, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 12, 2012
Real-time monitoring of breath ammonia during haemodialysis: use of ion mobility spectrometry (IMS) and cavity ring-down spectroscopy (CRDS) techniquesGiovanni Neri, Antonio Lacquaniti, Giuseppe Rizzo, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutationsElisabetta Tabolacci, Umberto Moscato, Francesca Zalfa, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndromeMarcella Zollino, Fiorella Gurrieri, Daniela Orteschi, et al.
Scientific Reports|March 11, 2017
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C SyndromesRoser Urreizti, Anna Maria Cueto-Gonzalez, Héctor Franco-Valls, et al.
Journal of Medical Case Reports|June 22, 2011
Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case reportLaura Travan, Vanna Pecile, Mariacristina Fertz, et al.
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