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Medical Hypotheses|May 16, 2019
Is infrared thermography (IRT) a possible tool for the evaluation and follow up of Emery-Dreifuss muscular dystrophy? A preliminary studyA Cabizosu, N Carboni, A Figus, et al.Medical Hypotheses|July 25, 2018
Theoretical basis for a new approach of studying Emery-Dreifuss muscular dystrophy by means of thermographyA Cabizosu, N Carboni, A Martinez-Almagro Andreo, et al.Medical Hypotheses|November 13, 2020
Relationship between infrared skin radiation and functional tests in patients affected by Emery-Dreifuss muscular dystrophy: Part 2A Cabizosu, R Berenguer-Vidal, J M Vegara-Meseguer, et al.Journal of Affective Disorders|August 26, 2022
The Perinatal Assessment of Paternal Affectivity (PAPA): Italian validation of a new tool for the screening of perinatal depression and affective disorders in fathersF Baldoni, M Giannotti, G Casu, et al.Human Genetics|August 21, 2001
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traitsA Angius, P M Melis, L Morelli, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 11, 2022
Fetal neurosonography at 31-35 weeks reveals altered cortical development in pre-eclampsia with and without small-for-gestational-age fetusA Basso, L Youssef, A Nakaki, et al.American Journal of Human Genetics|April 20, 2001
Identification of a new candidate locus for uric acid nephrolithiasisM N Ombra, P Forabosco, S Casula, et al.European Psychiatry : the Journal of the Association of European Psychiatrists|July 31, 2009
A comparison of continuous subcutaneous paliperidone infusion and repeated subcutaneous injection of risperidone free-base in ratsG Marchese, B Pittau, G Casu, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2000
Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucomaA Angius, P Spinelli, G Ghilotti, et al.Clinical Genetics|March 7, 2018
EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorderJ Lévy, D Haye, N Marziliano, et al.Pageof 3