Laia Alsina chercheuse
Alsina, Laia
VIAF ID: 13165809708558972870 (Personal)
Permalink: http://viaf.org/viaf/13165809708558972870
Preferred Forms
- 100 1 _ ‡a Alsina, Laia
- 100 0 _ ‡a Laia Alsina ‡c chercheuse
4xx's: Alternate Name Forms (7)
5xx's: Related Names (1)
- 510 2 _ ‡a Universitat de Barcelona ‡b Clinical Immunology Department ‡4 affi ‡4 https://d-nb.info/standards/elementset/gnd#affiliation ‡e Affiliation
Works
Title | Sources |
---|---|
A 10% liquid immunoglobulin preparation for intravenous use (Privigen®) in paediatric patients with primary immunodeficiencies and hypersensitivity to IVIG. | |
Ampliación del cribado neonatal a la detección de inmunodeficiencias combinadas graves. Un imperativo moral | |
Association of Polymorphisms in IRAK1, IRAK4 and MyD88, and Severe Invasive Pneumococcal Disease | |
B Regulatory Cells: Players in Pregnancy and Early Life | |
Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations | |
Characterization of the Highly Prevalent Regulatory CD24hiCD38hi B-Cell Population in Human Cord Blood | |
Cholecystitis and nephrotic syndrome complicating Epstein-Barr virus primary infection. | |
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency | |
Clues to management of neonatally diagnosed BTK deficiency. | |
The European Society for Immunodeficiencies (ESID) registry 2014 | |
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond. | |
Evans Syndrome as First Manifestation of Primary Immunodeficiency in Clinical Practice. | |
The expansion of human T-bet high CD21 low B cells is T cell dependent | |
Fenotipos clínicos asociados a la deficiencia selectiva de IgA: revisión de 330 casos y propuesta de un protocolo de seguimiento | |
Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis | |
From Severe Combined Immunodeficiency to Omenn syndrome after hematopoietic stem cell transplantation in a RAG1 deficient family | |
Glutamine effects on heat shock protein 70 and interleukines 6 and 10: Randomized trial of glutamine supplementation versus standard parenteral nutrition in critically ill children | |
el guia | |
Humoral deficiency in three paediatric patients with genetic diseases | |
Immunological Changes in Blood of Newborns Exposed to Anti-TNF-α during Pregnancy | |
Immunomodulation in sepsis: the role of endotoxin removal by polymyxin B-immobilized cartridge | |
Impact of CD4 T cell count on the outcome of planned treatment interruptions in early-treated human immunodeficiency virus-infected children | |
Impaired cellular immune response to tetanus toxoid but not to cytomegalovirus in effectively HAART-treated HIV-infected children | |
IRF8 mutations and human dendritic-cell immunodeficiency | |
Kinetics of humoral deficiency in CART19-treated children and young adults with acute lymphoblastic leukaemia | |
Laboratory evaluation of the IFN-γ circuit for the molecular diagnosis of Mendelian susceptibility to mycobacterial disease. | |
The Long Road to Biologic Therapies for Asthma in Pediatric Patients | |
Long-term use of bisphosphonates in the treatment of HIV-related bone pain in perinatally infected pediatric patients | |
Massively parallel sequencing reveals maternal somatic IL2RG mosaicism in an X-linked severe combined immunodeficiency family. | |
Meningococcal Serogroup B Disease in Vaccinated Children | |
Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity | |
A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4 | |
Natural Killer Cell Receptors and Cytotoxic Activity in Phosphomannomutase 2 Deficiency (PMM2-CDG) | |
Neonatal pulmonary tuberculosis evolving to a destroyed lung. | |
[The new scenario of primary immunodeficiencies and the role of the clinical immunologist in the specialised clinic] | |
Non-Hodgkin lymphoma in pediatric patients with common variable immunodeficiency. | |
Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection | |
A novel form of human STAT1 deficiency impairing early but not late responses to interferons | |
The PedPAD study: boys predominate in the hypogammaglobulinaemia registry of the ESID online database | |
Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects | |
Picture of the Month—Quiz Case | |
Primary immunodeficiency associated with chromosomal aberration - an ESID survey | |
Pyogenic bacterial infections in humans with MyD88 deficiency | |
Recurrent invasive pneumococcal disease in children: underlying clinical conditions, and immunological and microbiological characteristics | |
Reply to correspondence letter by M. Korppi | |
Serum sIgG4, but not sIgA, is involved in induced and natural tolerance to egg allergens. | |
Severe BCG-osis Misdiagnosed as Multidrug-Resistant Tuberculosis in an IL-12Rβ1-Deficient Peruvian Girl | |
Severe hypersplenism associated to hemophagocytic and lymphoproliferative syndrome secondary to Epstein-Barr virus infection. A report of two cases | |
Síndromes hemofagocíticos: la importancia del diagnóstico y tratamiento precoces | |
Single-cycle rituximab-induced immunologic changes in children: Enhanced in neuroimmunologic disease? | |
Sirolimus as an alternative treatment in patients with granulomatous-lymphocytic lung disease and humoral immunodeficiency with impaired regulatory T cells. | |
Surveillance study on the tolerability and safety of Flebogamma® DIF (10% and 5% intravenous immunoglobulin) in adult and pediatric patients | |
Systems scale interactive exploration reveals quantitative and qualitative differences in response to influenza and pneumococcal vaccines | |
Toll-like receptor 3 deficiency in autoimmune encephalitis post-herpes simplex encephalitis | |
Unexpected Relevant Role of Gene Mosaicism in Primary Immunodeficiency Diseases |