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LUIGI NOTARANGELO, M.D.
M.D.
Pediatric Allergy/Immunology Physician
NPI: 1093984064Individual
Specialties, Licenses & Credentials
Pediatric Allergy/Immunology PhysicianPrimary
Pediatrics — Pediatric Allergy/Immunology
Code: 2080P0201X
234087(MA)
Research & Publications (20)
2nd Conference of the Robert A. Good immunology society primary immune deficiencies and immune reconstitution Harvard Medical Boston, November 16th, 17th.
PMID 19412575·Immunol Res·2009
8-other
Is it necessary to identify molecular defects in primary immunodeficiency disease?
PMID 18992927·J Allergy Clin Immunol·2008
6-review
Out of breath: GM-CSFRalpha mutations disrupt surfactant homeostasis.
PMID 19015311·J Exp Med·2008
7-preclinical
Cartilage-hair hypoplasia: molecular basis and heterogeneity of the immunological phenotype.
PMID 18978468·Curr Opin Allergy Clin Immunol·2008
6-review
Genetic causes of bronchiectasis: primary immune deficiencies and the lung.
PMID 17534129·Respiration·2007
6-review
Wiskott-Aldrich Syndrome: a model for defective actin reorganization, cell trafficking and synapse formation.
PMID 14499269·Curr Opin Immunol·2003
6-review
Primary immune deficiencies unravel the molecular basis of immune response.
PMID 14692236·Rev Clin Exp Hematol·2003
6-review
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia.
PMID 11877312·Blood·2002
5-case
Mutations in severe combined immune deficiency (SCID) due to JAK3 deficiency.
PMID 11668610·Hum Mutat·2001
6-review
Combined immunodeficiencies due to defects in signal transduction: defects of the gammac-JAK3 signaling pathway as a model.
PMID 10993286·Immunobiology·2000
6-review
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model.
PMID 11213805·Immunol Rev·2000
6-review
Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome.
PMID 19414857·Blood·2009
8-other
Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.
PMID 19419768·Mol Immunol·2009
8-other
A single-center experience in 20 patients with infantile malignant osteopetrosis.
PMID 19507210·Am J Hematol·2009
8-other
X-linked primary immunodeficiencies as a bridge to better understanding X-chromosome related autoimmunity.
PMID 19361956·J Autoimmun·2009
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 300 LONGWOOD AVE, FEGAN 6
BOSTON, MA 02115 - Phone
- (617) 919-2276
Quick Facts
- NPI
- 1093984064
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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