About: Laia Alsina

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) গবেষক (bn) 研究者 (ja) chercheuse (fr) investigadora (es) ഗവേഷക (ml) дослідниця (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) onderzoeker (nl) researcher (en-ca) researcher (en-gb) researcher (en-us) hulumtuese (sq) ricercatrice (it) investigadora (ca) investigadora (gl) investigadora (pt) investigadora (ast)
rdfs:label	Laia Alsina (de) Laia Alsina (en) Laia Alsina (es) Laia Alsina (fr) Laia Alsina (nl) Laia Alsina (sl) Laia Alsina (ast)
skos:prefLabel	Laia Alsina (de) Laia Alsina (en) Laia Alsina (es) Laia Alsina (fr) Laia Alsina (nl) Laia Alsina (sl) Laia Alsina (ast)
name	Laia Alsina (de) Laia Alsina (en) Laia Alsina (es) Laia Alsina (fr) Laia Alsina (nl) Laia Alsina (sl) Laia Alsina (ast)
given name	wds:Q41472612-E10F6F4F-1D2A-4B6F-B2AE-973039E3DA6E
given name	Laia
instance of	wds:Q41472612-CA5C6071-B678-4FCF-BE21-0C23046EA366
instance of	Homo sapiens
Loop ID	wds:Q41472612-95943076-225E-4E31-9263-2EC52EAA743E
Loop ID	402953
skos:altLabel	Laia Alsina Manrique de Lara (en) Laia Alsina-Manrique (en)
occupation	wds:Q41472612-0F997ED8-A82E-4392-A29A-69DEF4138674
employer	wds:Q41472612-48D84AE1-1FF5-40B1-AFBF-108A84F3DF7A
sex or gender	wds:Q41472612-D22FE738-81EB-4C63-B792-C68AAA043F6C
VIAF ID	wds:Q41472612-93a3337f-7a26-45e2-8195-c6627284d196
GND ID	wds:Q41472612-a26200b3-b6ac-4036-8fd5-ccace958136f
IMDb ID	wds:Q41472612-cab753f3-4ba3-1a62-7887-c64df3cf59e6
educated at	wds:Q41472612-8780399D-0477-439B-B0A3-4BB8CD7B6991
family name	wds:Q41472612-114A6B2F-1055-4D93-889B-FD4E6131588F
VIAF ID	http://viaf.org/viaf/13165809708558972870
GND ID	https://d-nb.info/gnd/1262265673
occupation	researcher
employer	Hospital Sant Joan de Déu Barcelona
sex or gender	female organism
VIAF ID	13165809708558972870
GND ID	1262265673
IMDb ID	nm3761985
educated at	Lycée Français de Barcelone
family name	Alsina
ORCID iD	wds:Q41472612-8853F3D9-0773-4F05-BCD9-C72B7936B3D4
ORCID iD	https://orcid.org/0000-0002-3559-0018
ORCID iD	0000-0002-3559-0018
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q41472612
is author of	IRF8 mutations and human dendritic-cell immunodeficiency 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 Pyogenic bacterial infections in humans with MyD88 deficiency Immunomodulation in sepsis: the role of endotoxin removal by polymyxin B-immobilized cartridge Systems scale interactive exploration reveals quantitative and qualitative differences in response to influenza and pneumococcal vaccines Herpes simplex virus encephalitis in a patient with complete TLR3 deficiency: TLR3 is otherwise redundant in protective immunity Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency Massively parallel sequencing reveals maternal somatic IL2RG mosaicism in an X-linked severe combined immunodeficiency family. A novel form of human STAT1 deficiency impairing early but not late responses to interferons Recurrent invasive pneumococcal disease in children: underlying clinical conditions, and immunological and microbiological characteristics Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4 B Regulatory Cells: Players in Pregnancy and Early Life Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects The European Society for Immunodeficiencies (ESID) registry 2014 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 Toll-like receptor 3 deficiency in autoimmune encephalitis post-herpes simplex encephalitis Evans Syndrome as First Manifestation of Primary Immunodeficiency in Clinical Practice. Characterization of the Highly Prevalent Regulatory CD24hiCD38hi B-Cell Population in Human Cord Blood Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond. Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity Serum allergen-specific IgA is not associated with natural or induced tolerance to egg in children Surveillance study on the tolerability and safety of Flebogamma® DIF (10% and 5% intravenous immunoglobulin) in adult and pediatric patients

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