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Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|June 16, 2010
Hepatitis B virus in Buenos Aires, Argentina: genotypes, virological characteristics and clinical outcomesS C Pezzano, C Torres, H A Fainboim, et al.
Clinical Genetics|October 2, 2009
Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literatureC Nemos, L Lambert, F Giuliano, et al.
Neurology|January 26, 2006
Efficacy and safety of vardenafil in men with erectile dysfunction caused by spinal cord injuryF Giuliano, E Rubio-Aurioles, M Kennelly, et al.
Minerva Cardiology and Angiology|March 11, 2021
Safety of reduced or absent antithrombotic therapy after left atrial appendage closure in patients affected by hereditary hemorrhagic telangiectasia and atrial fibrillationMartino Pepe, Patrizia Suppressa, Antonio F Giuliano, et al.
Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.
International Journal of Clinical Practice|February 12, 2008
Cardiovascular outcomes among sildenafil users: results of the International Men's Health StudyM A Mittleman, M Maclure, M A Lewis, et al.
Molecular Psychiatry|April 19, 2021
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disordersE El Khouri, J Ghoumid, D Haye, et al.
Clinical Genetics|October 19, 2010
The Renpenning syndrome spectrum: new clinical insights supported by 13 new PQBP1-mutated malesD Germanaud, M Rossi, G Bussy, et al.
Scientific Reports|December 3, 2017
Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patientsD Baux, C Vaché, C Blanchet, et al.
The British Journal of Dermatology|August 25, 2018
Dermatological manifestations in cardiofaciocutaneous syndrome: a prospective multicentric study of 45 mutation-positive patientsD Bessis, F Morice-Picard, E Bourrat, et al.
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