Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Michael S. Borzy"'
Autor:
Michael S. Borzy, Karin Chen, P. Nagesh Rao, Najib Aziz, Jack Gorski, Sean A. McGhee, Maria Garcia-Lloret, Michael H. Land, E. Richard Stiehm
Publikováno v:
Journal of Allergy and Clinical Immunology. 120:908-915
Background Therapeutic options for DiGeorge syndrome (DGS) with profound T-cell deficiency are very limited. Thymic transplantation has shown promising results but is not easily available. Hematopoietic cell transplantation (HCT) has been successful
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92558ebed8ad6057a36c83707b94b2fa
https://doi.org/10.1016/j.jaci.2007.08.048
https://doi.org/10.1016/j.jaci.2007.08.048
Autor:
Ann M. Reed, Lawrence S. Zemel, Norman T. Ilowite, Michael S. Borzy, Kathy Abbott, Alan R. Dyer, Christy Sandborg, Rosalind Ramsey-Goldman, Jonathan D. Gitlin, Rafael Rivas-Chacon, Larry B. Vogler, Eduardo P. Mendez, Christine Hom, Rebecca B. Lipton, Abraham Gedalia, Gail Cawkwell, Lauren M. Pachman, Deborah Mc Curdy, Eli Shamiyeh
Publikováno v:
Arthritis & Rheumatism. 53:166-172
Objective To obtain data concerning a history of infection occurring in the 3 months before recognition of the typical weakness and rash associated with juvenile dermatomyositis (JDM). Methods Parents or caretakers of children within 6 months of JDM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda17ebb67cbc31cdd2b309eed5e8083
https://doi.org/10.1002/art.21068
https://doi.org/10.1002/art.21068
Autor:
Michael S. Borzy, Rick A. Wetsel, Marja Liisa Lokki, Lori Singer, Michelle L. Van Hee, Judit Kramer
Publikováno v:
Clinical Immunology and Immunopathology. 81:244-252
To determine the molecular basis of complement C3 deficiency in a Laotian kindred, the homozygous C3-deficient male propositus was studied. By ELISA, this individual's serum was determined to contain approximately 4 microg/ml C3 (0.3% of normal). In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eba52f900b41e839aa24ed5097b6af23
https://doi.org/10.1006/clin.1996.0185
https://doi.org/10.1006/clin.1996.0185
Publikováno v:
Journal of Clinical Immunology. 11:357-362
A child with disseminated disease due to Mycobacterium avium had progressive disease in spite of 4.5 years of therapy with multiple antimicrobial agents selected on the basis of in vitro sensitivity testing of her organism. A defect in monocyte bacte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ac755ed957825e455f413f856f05644
https://doi.org/10.1007/bf00918801
https://doi.org/10.1007/bf00918801
Autor:
Michael S. Borzy, Stephen Schneider
Publikováno v:
Clinical Pediatrics. 35:147-149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816bc47583d17b4a17409c8d7467da18
https://doi.org/10.1177/000992289603500306
https://doi.org/10.1177/000992289603500306
Publikováno v:
Journal of Allergy and Clinical Immunology. 121:1063-1064
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12950a07db8f5988e1f0c5dfd9194c24
https://doi.org/10.1016/j.jaci.2007.12.1182
https://doi.org/10.1016/j.jaci.2007.12.1182
Publikováno v:
Pediatric nephrology (Berlin, Germany). 12(8)
We describe a patient with immune complex-mediated glomerulonephritis and leukocytoclastic vasculitis associated with Epstein-Barr virus (EBV) infectious mononucleosis. The patient required hemodialysis and has residual hypertension. This case implic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db66a6a3548a1c98672cb2f011df3617
https://pubmed.ncbi.nlm.nih.gov/9811388
https://pubmed.ncbi.nlm.nih.gov/9811388
Publikováno v:
American Journal of Medical Genetics. 18:527-539
Chromosomal heteromorphisms defined by the quinacrine banding technique were used to identify the maternal origin of 46,XX lymphocytes present in the blood of a male infant with severe combined immune deficiency disease. These chromosomal markers wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd65a39ec25e38bfaa1492f919bd3c73
https://doi.org/10.1002/ajmg.1320180321
https://doi.org/10.1002/ajmg.1320180321
Autor:
Michael S. Borzy, Donald C. Houghton
Publikováno v:
American Journal of Kidney Diseases. 5:54-59
The renal histopathology of a 7-year-old Laotian male with inherited deficiency of the third component of complement, recurrent infections, and persistent hematuria and proteinuria is described. The histologic changes are predominantly those of mesan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2bc0898b8ed254e923d74d98d10a68
https://doi.org/10.1016/s0272-6386(85)80137-2
https://doi.org/10.1016/s0272-6386(85)80137-2