cfranco@vhebron.net
FRANCO JARAVA, CLARA
iMarina ID: 04-330432Servei
Immunologia. Hospital Universitari Vall d'Hebron. Passeig de la Vall d'Hebron. Barcelona. 08035
Codis d'identificació
Cronologia
juliol de 2017
Doctorat: Programa Oficial de Doctorado en Inmunología Avanzada
Universitat Autònoma de Barcelona
gener de 2011
Titulat superior / Grau: Licenciado en Biotecnología
Universitat Rovira i Virgili
Cronologia
juliol de 2016
Facultatiu especialista
Hospital Universitari Vall d'Hebron. Immunologia
2016 -
maig de 2012
Biólogo Interno Residente (Formación Sanitaria Especializada). Hospital Universitario Vall d'Hebron
Hospital Universitario Vall D'Hebron
2012 - 2016
novembre de 2011
Estudiante en prácticas. FUNDACIO PRIVADA INSTITUT DINVESTIGACIO SANITARIA PERE VIRGILI
FUNDACIO PRIVADA INSTITUT DINVESTIGACIO SANITARIA PERE VIRGILI
2011 - 2011
Reconeixements Investigació
Reconeixements Docents
Transferència
Projectes R+D+I
Direcció y participació en projectes
IP
NO IP
Grup de Recerca
Activitat docent
Centres
FUNDACIO INSTITUT DE RECERCA DE L'HOSPITAL UNIV. VALL D'HEBRON
Universitat Rovira i Virgili
Universitat Autònoma de Barcelona
Societat Catalana de Pediatria
Fundació Hospital Universitari Vall d'Hebron Institut de Recerca (VHIR)
European Society of Immunodeficiency Diseases
Charles Univeristy in Prague
Assignatura/Curs
Altmetría
| 2021 | Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in th... | |
| 2020 | Uncovering Low-Level Maternal Gonosomal Mosaicism in X-Linked Agammaglobulinemia... | |
| 2020 | Serum IL-10 Levels and Its Relationship with Parasitemia in Chronic Chagas Disea... | |
| 2020 | The IL-2RG R328X nonsense mutation allows partial STAT-5 phosphorylation and def... | |
| 2019 | Serum protein electrophoresis and complement deficiencies: a veteran but very ve... | |
| 2019 | Extended immunophenotyping reference values in a healthy pediatric population | |
| 2019 | Unexpected Relevant Role of Gene Mosaicism in Primary Immunodeficiency Diseases. | |
| 2018 | LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome ... | |
| 2018 | TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a ... | |
| 2018 | Th1-skewed profile and excessive production of proinflammatory cytokines in a NF... | |
| 2018 | LRBA deficiency in a patient with a novel homozygous mutation due to chromosome ... | |
| 2017 | Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Conseque... | |
| 2017 | Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to... | |
| 2017 | How clinical laboratory standard capillary protein electrophoresis alerted to a ... | |
| 2017 | Complement factor 5 (C5) p.A252T mutation is prevalent in, but not restricted to... | |
| 2016 | Novel Mutations Causing C5 Deficiency in Three North-African Families. | |
| 2016 | Clinical laboratory standard capillary protein electrophoresis alerted of a low ... | |
| 2016 | Novel Mutations Causing C5 Deficiency in Three North-African Families |
Xarxa de Col·laboració
