Your browser doesn't support javascript.
loading
Hereditary Deficiency of the Second Component of Complement: Early Diagnosis and 21-Year Follow-Up of a Family.
Dellepiane, Rosa Maria; Baselli, Lucia Augusta; Cazzaniga, Marco; Lougaris, Vassilios; Macor, Paolo; Giordano, Mara; Gualtierotti, Roberta; Cugno, Massimo.
Affiliation
  • Dellepiane RM; Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, 20122 Milan, Italy.
  • Baselli LA; Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, 20122 Milan, Italy.
  • Cazzaniga M; Department of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, 20122 Milan, Italy.
  • Lougaris V; Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, Department of Clinical and Experimental Sciences, University of Brescia and Spedali Civili di Brescia, 25121 Brescia, Italy.
  • Macor P; Department of Life Sciences, University of Trieste, 34123 Trieste, Italy.
  • Giordano M; Department of Health Sciences, Laboratory of Genetics, University of Eastern Piedmont and Interdisciplinary Research Center of Autoimmune Diseases, 28100 Novara, Italy.
  • Gualtierotti R; Internal Medicine, Department of Pathophysiology and Transplantation, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Cugno M; Internal Medicine, Department of Pathophysiology and Transplantation, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy.
Medicina (Kaunas) ; 56(3)2020 Mar 10.
Article in En | MEDLINE | ID: mdl-32164349
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement C2 / Family / Aftercare / Genetic Diseases, Inborn Type of study: Diagnostic_studies / Screening_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Medicina (Kaunas) Journal subject: MEDICINA Year: 2020 Document type: Article Affiliation country: Italy Country of publication: Switzerland
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Complement C2 / Family / Aftercare / Genetic Diseases, Inborn Type of study: Diagnostic_studies / Screening_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Medicina (Kaunas) Journal subject: MEDICINA Year: 2020 Document type: Article Affiliation country: Italy Country of publication: Switzerland