Zobrazeno 1 - 10
of 38
pro vyhledávání: '"M E, Conley"'
Publikováno v:
Clinical Infectious Diseases. 39:e17-e20
A patient with respiratory syncytial virus (RSV) infection and severe combined immunodeficiency was studied during a 3-month period of bone marrow transplantation and palivizumab infusion. No RSV isolates with palivizumab escape mutations were identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e698cef3834b0eda40e8fdc80e018172
https://doi.org/10.1086/421779
https://doi.org/10.1086/421779
Autor:
Julia L. Hurwitz, Ely Benaim, M. E. Conley, Laura C. Bowman, Y.-J. Gan, Barrett G. Haik, Jesse J. Jenkins, P. H. Spiegel, J. W. Sixbey, Karen S. Slobod, John T. Sandlund, Rose Mary S. Stocks
Publikováno v:
Clinical Infectious Diseases. 31:184-188
Ocular manifestations have been attributed to the Epstein-Barr virus (EBV), largely on the basis of seroepidemiologic data. Two patients who developed conjunctival disease as the presenting feature of EBV infection are reported, each confirmed by in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::782695959dba258e82f7318549289b54
https://doi.org/10.1086/313932
https://doi.org/10.1086/313932
Publikováno v:
Conference on Applied Statistics in Agriculture.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06829cab68f470b283d9632a6f62ca9a
https://doi.org/10.4148/2475-7772.1128
https://doi.org/10.4148/2475-7772.1128
Autor:
M E, Conley
Publikováno v:
Reviews in immunogenetics. 2(2)
The primary immunodeficiencies are a heterogeneous group of disorders that affect either the development or the function of the immune system. In the last ten years, the genes responsible for many of the most common and best studied immunodeficiencie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::852dc0a8840f28b0fad52c0fcb2ea821
https://pubmed.ncbi.nlm.nih.gov/11258420
https://pubmed.ncbi.nlm.nih.gov/11258420
Publikováno v:
Immunological reviews. 178
Patients with genetic defects in B-cell development provide an unusual opportunity to dissect the requirements for normal B-cell maturation. It is striking that all of the known genetic defects that result in a failure of B-cell development involve s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::de9ea548b58122b1da5acd2f00dadbf8
https://pubmed.ncbi.nlm.nih.gov/11213809
https://pubmed.ncbi.nlm.nih.gov/11213809
Publikováno v:
Clinical immunology (Orlando, Fla.). 93(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e82f093e28f7253a8e1775b025647937
https://pubmed.ncbi.nlm.nih.gov/10600329
https://pubmed.ncbi.nlm.nih.gov/10600329
Autor:
J, Rohrer, M E, Conley
Publikováno v:
Blood. 94(10)
Gene therapy for inherited disorders is more likely to succeed if gene-corrected cells have a proliferative or survival advantage compared with mutant cells. We used a competitive reconstitution model to evaluate the strength of the selective advanta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49ddf7dfda647c675633a2c4f9d53cec
https://pubmed.ncbi.nlm.nih.gov/10552945
https://pubmed.ncbi.nlm.nih.gov/10552945
Publikováno v:
Human mutation. 13(4)
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton agammaglobulinemia tyrosine kinase (BTK). A database (BTKbase) of BTK mutations lists 544 mutation entries from 471 unrelated families showing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5c884d7a383d97be960df169c56b4b8f
https://pubmed.ncbi.nlm.nih.gov/10220140
https://pubmed.ncbi.nlm.nih.gov/10220140
Publikováno v:
Conference on Applied Statistics in Agriculture.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::309ea5ee955fb0f237c23e8ee63253ef
https://doi.org/10.4148/2475-7772.1263
https://doi.org/10.4148/2475-7772.1263
Autor:
F X, Arrendondo-Vega, I, Santisteban, L D, Notarangelo, J, El Dahr, R, Buckley, C, Roifman, M E, Conley, M S, Hershfield
Publikováno v:
Human mutation. 11(6)
The degree of immunodeficiency associated with deficiency of adenosine deaminase (ADA) is variable. Most patients are infants with severe combined immunodeficiency (SCID), but in about 20 percent immune dysfunction becomes manifest later in childhood
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb7494bfa3618fcc7fab715feb3358ad
https://pubmed.ncbi.nlm.nih.gov/10200056
https://pubmed.ncbi.nlm.nih.gov/10200056