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Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study.
Putotto, Carolina; Pulvirenti, Federica; Pugnaloni, Flaminia; Isufi, Ina; Unolt, Marta; Anaclerio, Silvia; Caputo, Viviana; Bernardini, Laura; Messina, Elisa; Moretti, Corrado; Tarani, Luigi; Marino, Bruno; Versacci, Paolo.
Affiliation
  • Putotto C; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Pulvirenti F; Regional Reference Centre for Primary Immune Deficiencies, Azienda Ospedaliera Universitaria Policlinico Umberto I, 00185 Rome, Italy.
  • Pugnaloni F; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Isufi I; Neonatal Intensive Care Unit, Medical and Surgical Department of Fetus, Newborn and Infant-Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
  • Unolt M; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Anaclerio S; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Caputo V; Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital IRCCS, 00165 Rome, Italy.
  • Bernardini L; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Messina E; Department of Experimental Medicine, Sapienza University of Rome, 00161 Rome, Italy.
  • Moretti C; Cytogenetics Unit, Casa Sollievo della Sofferenza Foundation, San Giovanni Rotondo, 71013 Foggia, Italy.
  • Tarani L; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Marino B; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
  • Versacci P; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Genes (Basel) ; 13(12)2022 12 10.
Article in En | MEDLINE | ID: mdl-36553601
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DiGeorge Syndrome Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: Country of publication: