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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 13, 2021
The earliest depictions of a PIK3CA-Related Overgrowth Spectrum disorder: 17th-18th century prints of women with severe limb overgrowthThomas F Heyne, Giovanni Neri, Angela E LinGenes|October 27, 2022
Phenotypic Spectrum and Molecular Findings in 17 ATR-X Syndrome Italian Patients: Some New InsightsAlessandro Vaisfeld, Sara Taormina, Alessandro Simonati, et al.The Journal of Clinical Investigation|December 4, 2012
Fragile X syndrome: causes, diagnosis, mechanisms, and therapeuticsClaudia Bagni, Flora Tassone, Giovanni Neri, et al.Pain|December 4, 2023
Remifentanil-induced hyperalgesia in healthy volunteers: a systematic review and meta-analysis of randomized controlled trialsCinzia Dello Russo, Valeria Di Franco, Elisabetta Tabolacci, et al.American Journal of Medical Genetics. Part A|February 21, 2008
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boysM Giulia Torrioli, Silvia Vernacotola, Laura Peruzzi, et al.American Journal of Medical Genetics. Part A|June 18, 2016
Recognizable facial features in patients with alternating hemiplegia of childhoodFiorella Gurrieri, Francesco Danilo Tiziano, Giuseppe Zampino, et al.American Journal of Medical Genetics|December 28, 2002
Limb anomalies: Developmental and evolutionary aspectsFiorella Gurrieri, Klaus W Kjaer, Eugenio Sangiorgi, et al.Sensors (Basel, Switzerland)|October 24, 2018
Photo-Electrochemical Sensing of Dopamine by a Novel Porous TiO₂ Array-Modified Screen-Printed Ti ElectrodeFrancesco Tavella, Claudio Ampelli, Salvatore Gianluca Leonardi, et al.European Journal of Human Genetics : EJHG|January 17, 2008
XLMR genes: update 2007Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, et al.Cancer Biomarkers : Section a of Disease Markers|December 29, 2006
The use of microsatellite instability, immunohistochemistry and other variables in determining the clinical significance of MLH1 and MSH2 unclassified variants in Lynch syndromeEmanuela Lucci-Cordisco, Luigi Boccuto, Giovanni Neri, et al.Pageof 30