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LAIA ALLENDE, M.D.
M.D.
Surgery Physician
NPI: 1225235419Individual
Specialties, Licenses & Credentials
Surgery PhysicianPrimary
Surgery
Code: 208600000X
18226(PR)
Research & Publications (20)
Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.
PMID 17658607·Mol Immunol·2008
8-other
Pharmacoepidemiological approach to the predisposing factors for highly active antiretroviral therapy failure in an HIV-positive cohort from Cordoba City (Argentina) 1995-2005.
PMID 18482965·Int J STD AIDS·2008
8-other
Cell cycle regulation by FasL and Apo2L/TRAIL in human T-cell blasts. Implications for autoimmune lymphoproliferative syndromes.
PMID 18483205·J Leukoc Biol·2008
8-other
Identification of novel non-pathogenic mutation in SH3 domain of Btk in an XLA patient.
PMID 17707910·Mol Immunol·2008
8-other
Longitudinal analysis of immune function in the first 3 years of life in thymectomized neonates during cardiac surgery.
PMID 18811694·Clin Exp Immunol·2008
8-other
The induction of Bim expression in human T-cell blasts is dependent on nonapoptotic Fas/CD95 signaling.
PMID 17062728·Blood·2007
8-other
Autoimmune lymphoproliferative syndrome (ALPS) in a patient with a new germline Fas gene mutation.
PMID 17336828·Immunobiology·2007
5-case
Effects of the herbicide Roundup on freshwater microbial communities: a mesocosm study.
PMID 18213971·Ecol Appl·2007
8-other
Peripheral blood lymphocyte populations in end-stage liver diseases.
PMID 17667057·J Clin Gastroenterol·2007
8-other
Rapid molecular prenatal diagnosis of ataxia-telangiectasia by direct mutational analysis.
PMID 17600866·Prenat Diagn·2007
8-other
Differential biological role of CD3 chains revealed by human immunodeficiencies.
PMID 17277165·J Immunol·2007
5-case
A novel RMRP mutation in a Spanish patient with cartilage-hair hypoplasia.
PMID 17015150·Immunobiology·2006
5-case
Familial hemophagocytic lymphohistiocytosis in an adult patient homozygous for A91V in the perforin gene, with tuberculosis infection.
PMID 16956828·Haematologica·2006
5-case
A homozygous Fas ligand gene mutation in a patient causes a new type of autoimmune lymphoproliferative syndrome.
PMID 16627752·Blood·2006
5-case
Rapid molecular diagnosis of ataxia-telangiectasia by optimised RT-PCR and direct sequencing analysis.
PMID 16164035·Immunobiology·2005
8-other
Partial immune reconstitution after bone marrow transplantation in a boy with recombination activating gene 1 defect.
PMID 14990985·Bone Marrow Transplant·2004
5-case
A genetic study of cathepsin C gene in two families with Papillon-Lefèvre syndrome.
PMID 12809647·Mol Genet Metab·2003
8-other
Mutations of CD40 ligand in two patients with hyper-IgM syndrome.
PMID 12952351·Immunobiology·2003
5-case
A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency.
PMID 11139207·Clin Diagn Lab Immunol·2001
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- ST#1 PASEO MAYOR D5
RIO PIEDRAS, PR 00926 - Phone
- (787) 413-5163
Quick Facts
- NPI
- 1225235419
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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