Detalhe da pesquisa
1.
Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions.
N Engl J Med
; 366(4): 330-8, 2012 Jan 26.
Artigo
Inglês
| MEDLINE | ID: mdl-22236196
2.
Mastocytosis associated with a rare germline KIT K509I mutation displays a well-differentiated mast cell phenotype.
J Allergy Clin Immunol
; 134(1): 178-87, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24582309
3.
GATA-2-deficient mast cells limit IgE-mediated immediate hypersensitivity reactions in human subjects.
J Allergy Clin Immunol
; 144(2): 613-617.e14, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-31102699
4.
Diminished allergic disease in patients with STAT3 mutations reveals a role for STAT3 signaling in mast cell degranulation.
J Allergy Clin Immunol
; 132(6): 1388-96, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24184145
5.
Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities.
J Allergy Clin Immunol
; 133(5): 1471-4, 2014 May.
Artigo
Inglês
| MEDLINE | ID: mdl-24472624
6.
Inflammatory Markers of the Systemic Capillary Leak Syndrome (Clarkson Disease).
J Clin Cell Immunol
; 5: 1000213, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25405070
7.
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease).
Rare Dis
; 1(1)2013 Dec 12.
Artigo
Inglês
| MEDLINE | ID: mdl-24808988
8.
Selective depletion of alloreactive donor lymphocytes: a novel method to reduce the severity of graft-versus-host disease in older patients undergoing matched sibling donor stem cell transplantation.
Blood
; 106(3): 1123-9, 2005 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-15817673
9.
A pilot study of the recombinant soluble human tumour necrosis factor receptor (p75)-Fc fusion protein in patients with myelodysplastic syndrome.
Br J Haematol
; 117(1): 119-26, 2002 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-11918541