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JENNIFER PUCK, M.D.
M.D.
Pediatric Allergy/Immunology Physician
NPI: 1871525378Individual
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
G87720(CA)
Pediatric Allergy/Immunology PhysicianPrimary
Pediatrics — Pediatric Allergy/Immunology
Code: 2080P0201X
G87720(CA)
Research & Publications (20)
Population-based newborn screening for severe combined immunodeficiency.
PMID 19418625·Biol Blood Marrow Transplant·2008
6-review
Population-based newborn screening for severe combined immunodeficiency: steps toward implementation.
PMID 17931561·J Allergy Clin Immunol·2007
8-other
Severe combined immunodeficiency: new advances in diagnosis and treatment.
PMID 17917011·Immunol Res·2007
8-other
Neonatal screening for severe combined immune deficiency.
PMID 17989529·Curr Opin Allergy Clin Immunol·2007
6-review
Use of rituximab for refractory cytopenias associated with autoimmune lymphoproliferative syndrome (ALPS).
PMID 19214977·Pediatr Blood Cancer·2009
8-other
Treatment of patients with new onset Type 1 diabetes with a single course of anti-CD3 mAb Teplizumab preserves insulin production for up to 5 years.
PMID 19443276·Clin Immunol·2009
2-rct
Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a Coronin-1A mutation and a chromosome 16p11.2 deletion.
PMID 19097825·Clin Immunol·2009
5-case
Allogeneic hematopoietic cell transplantation for primary immune deficiency diseases: current status and critical needs.
PMID 18992926·J Allergy Clin Immunol·2008
8-other
Mutations causing severe combined immunodeficiency: detection with a custom resequencing microarray.
PMID 18641513·Genet Med·2008
8-other
The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.
PMID 18836449·Nat Immunol·2008
7-preclinical
Hematopoietic stem cell transplantation for severe combined immunodeficiency diseases.
PMID 18162224·Biol Blood Marrow Transplant·2008
6-review
Complementation of a pathogenic IFNGR2 misfolding mutation with modifiers of N-glycosylation.
PMID 18625743·J Exp Med·2008
5-case
Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee.
PMID 17952897·J Allergy Clin Immunol·2007
8-other
IL-7 receptor deficient SCID with a unique intronic mutation and post-transplant autoimmunity due to chronic GVHD.
PMID 17827065·Clin Immunol·2007
5-case
Primary immunodeficiency: meeting the challenges.
PMID 17931558·J Allergy Clin Immunol·2007
7-preclinical
The hyper-IgE syndrome is not caused by a microdeletion syndrome.
PMID 18000661·Immunogenetics·2007
8-other
Pyrimethamine treatment does not ameliorate lymphoproliferation or autoimmune disease in MRL/lpr-/- mice or in patients with autoimmune lymphoproliferative syndrome.
PMID 17674358·Am J Hematol·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1825 FOUTH STREET, 6TH FLOOR, IMMUNOLOGY CENTER
SAN FRANCISCO, CA 94158 - Phone
- (415) 502-2090
Quick Facts
- NPI
- 1871525378
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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