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PATRICK MELLA, MD
MD
Internal Medicine Physician
NPI: 1982915781IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
ME121444(FL)
Education
OTHER
Class of 2010
Research & Publications (15)
Common polymorphisms of the growth hormone (GH) receptor do not correlate with the growth response to exogenous recombinant human GH in GH-deficient children.
PMID 16394090·J Clin Endocrinol Metab·2006
8-other
Cytokine-mediated signalling and early defects in lymphoid development.
PMID 16264332·Curr Opin Allergy Clin Immunol·2005
6-review
Mutations of the Wiskott-Aldrich Syndrome Protein (WASP): hotspots, effect on transcription, and translation and phenotype/genotype correlation.
PMID 15284122·Blood·2004
8-other
Eleven novel JAK3 mutations in patients with severe combined immunodeficiency-including the first patients with mutations in the kinase domain.
PMID 11668621·Hum Mutat·2001
8-other
Unexpected and variable phenotypes in a family with JAK3 deficiency.
PMID 11781709·Genes Immun·2001
8-other
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
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.
PMID 10859027·Mol Med·2000
8-other
Molecular modeling of the Jak3 kinase domains and structural basis for severe combined immunodeficiency.
PMID 10900158·Clin Immunol·2000
8-other
[Prevalence of congenital malformations at birth and associated factors in Easter Island, Chile (1988-1998)].
PMID 10962884·Rev Med Chil·2000
8-other
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphism.
PMID 10982185·Hum Genet·2000
8-other
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterization.
PMID 10794431·Clin Immunol·2000
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
- 1839 CENTRAL AVE
SAINT PETERSBURG, FL 33713 - Phone
- (727) 322-1054
Quick Facts
- NPI
- 1982915781
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 16
- Publications
- 15
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