Search Results - "CHINEN, J."

Infections and immunodeficiency in Down syndrome by Ram, G, Chinen, J

“…Down syndrome (DS) is the most common genetic disease and presents with cognitive impairment, cardiac and gastrointestinal abnormalities, in addition to other…”
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Presentation of atopic disease in a large cohort of pediatric liver transplant recipients by Shroff, P., Mehta, R. S., Chinen, J., Karpen, S. J., Davis, C. M.

“…Shroff P, Mehta RS, Chinen J, Karpen SJ, Davis CM. Presentation of atopic disease in a large cohort of pediatric liver transplant recipients. :  Atopic disease…”
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Novel aspects of Kindlin‐3 function in humans based on a new case of leukocyte adhesion deficiency III by MELLER, J., MALININ, N. L., PANIGRAHI, S., KERR, B. A., PATIL, A., MA, Y., VENKATESWARAN, L., ROGOZIN, I. B., MOHANDAS, N., EHLAYEL, M. S., PODREZ, E. A., CHINEN, J., BYZOVA, T. V.

“…Background:  Kindlin‐3 is a novel integrin activator in hematopoietic cells, and its deficiency leads to immune problems and severe bleeding, known as…”
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Use of intravenous immunoglobulin in human disease: A review of evidence by members of the Primary Immunodeficiency Committee of the American Academy of Allergy, Asthma and Immunology by Orange, Jordan S., Hossny, Elham M., Weiler, Catherine R., Ballow, Mark, Berger, Melvin, Bonilla, Francisco A., Buckley, Rebecca, Chinen, Javier, El-Gamal, Yehia, Mazer, Bruce D., Nelson, Robert P., Patel, Dhavalkumar D., Secord, Elizabeth, Sorensen, Ricardo U., Wasserman, Richard L., Cunningham-Rundles, Charlotte

“…Human immunoglobulin prepared for intravenous administration (IGIV) has a number of important uses in the treatment of disease. Some of these are in diseases…”
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Immunodeficiency in Down Syndrome: Revisiting Recurrent Infections in the Post-Pneumococcal Vaccination Era by Ram, G, Ostermaier, K, Hanson, I.C, Chinen, J

“…Frequency of RI was significantly associated with history of allergic rhinitis/asthma (odds ratio [OR]:15.8 [95% confidence interval [CI]:4.3-58.5]), GERD…”
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A Novel Severe Combined Immunodeficiency (SCID) Mutation in Three Mexican Siblings with additional de novo Duchenne Muscular Dystrophy (DMD) mutation by Nicholas, S.K, Chinen, J, Martinez, C, Lotze, T, Adesina, A.M, Fishman, D.S, Krance, R.A, Hanson, I.C

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Decline of antibodies in XLA infant: when to start IVIG by Okocha, I. U., Hanson, C. G., Chinen, J., Shearer, W. T.

“…Maternal antibody levels in XLA neonates may predict when to start replacement IgG…”
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Post-Solid Organ Transplant Atopy Is Not Limited to Food Hypersensitivity by Shroff, P, Mehta, R.S, Chinen, J, Karpen, S.J, Davis, C.M

“…Chart review was performed on 176 liver transplant recipients for food allergy, asthma, allergic rhinitis, and allergic skin diseases…”
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Autoimmunity in a Cohort of 106 partial DiGeorge Syndrome Pediatric Patients by Tison, B, Davis, C.M, Abramson, S.L, Hanson, I, Nicolas, S, Paul, M.E, Seeborg, F, Shearer, W.T, Perez, M.D, Noroski, L.M, Chinen, J

“…Low CD4+45RA+ T cell percentages in infancy and low lymphoproliferative response to antigens may be associated to autoimmune disease in pDGS…”
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CMV Elimination in DiGeorge Syndrome Following Matched Related Stem Cell Transplant by Nguyen, D.K, Chinen, J, Krance, R.A, Stafford, W.W, Demmler, G.J, Hanson, I.C

“…CMV infection in complete DiGeorge Syndrome (DGS) patients has been associated with mortality prior and post thymus transplantation. Due to unavailability of…”
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Serum Interleukin-7 (IL-7) Level May Be a Marker of T-Cell Homeostasis in Partial DiGeorge Syndrome (pDGS) by Tantibhaedhyangkul, U, Davis, C.M, Noroski, L.M, Hanson, I.C, Shearer, W.T, Chinen, J

“…Blood samples of consecutive pDGS children with chromosome 22q11.2 deletion (median age: 45 months, range: 1-231 months) were analyzed for lymphocyte…”
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Correlation of Initial Clinical Presentation and Egg White Specific IgE Values in a Cohort of 104 Egg Allergic Patients by Wells, R.D, Chinen, J, Davis, C.M

“…Methods A retrospective chart review of the initial clinical symptoms (defined as the initial clinic visit), initial egg white-IgE, and initial total serum IgE…”
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Outcomes of 48 Severe Combined Immunodeficiency Patients Treated with Hematopoietic Stem Cell Transplantation at a Single Center Between 1981 and 2007 by Patel, N.C, Chinen, J, Rosenblatt, H.M, Hanson, I.C, Krance, R.A, Paul, M.E, Abramson, S.L, Noroski, L.M, Davis, C.M, Brown, B.S, Ritz, J, Shearer, W.T

“…From 1998 to 2007, 17 patients (median age at transplant 10 [range 1-108] mo) received conditioning treatment followed by MMRD or matched unrelated donor…”
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Skin prick test for anti-thymocyte globulin does not predict immediate ATG-related adverse events by Lugar, P.L., Parrino, J., Young, N., Chinen, J.

“…A chart review was conducted on 85 patients treated with horse ATG for aplastic anemia or myelodysplastic syndromes at the NIH from January 2002 to February…”
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M235 UNSUSPECTED CAUSE OF CHRONIC BILATERAL PALPEBRAL EDEMA IN A TODDLER 9140 by Chu, A., Moonat, H., Naik, N., Chinen, J.

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Lymphocyte Proliferation to Antigens Develops Over Time in Partial DiGeorge Syndrome by Kancherla, V.S, Reddy, A.P, Noroski, L.M, Chinen, J, Yeh, H.W, Davis, C.M

“…LPAs to mitogens did not change over the follow-up period (PHA, ConA, and PWM counts per minute (cpm), p= 0.46, 0.20, and 0.45, respectively) and LPAs to…”
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Basidiomycetous Inonotus (Phellinus) tropicalis Osteomyelitis in Pediatric and Adult X-linked Chronic Granulomatous Disease by Nguyen, D.K, Davis, C.M, Chinen, J, Vallejo, J.G, Noroski, L.M

“…MRI revealed marrow fluid collection at distal femoral diaphysis, consistent with osteomyelitis; initial biopsy culture resulted as Aspergillus sp. Methods and…”
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Ex vivo gene therapy of two children with X-linked severe combined immunodeficiency by Chinen, J., Davis, J., Linton, G.F., Theobald-Whitting, N.L., Woltz, P.C., Buckley, R.H., Malech, H.L., Puck, J.M.

“…Bone marrow transplantation (BMT) for XSCID is not fully satisfactory because most patients lack an HLA-matched relative and receive HLA-haploidentical BMTs,…”
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Skeletal anomalies in hyper-IgE recurrent infection syndrome (HIES, Job syndrome) by Chinen, J., Davis, J., Darnell, D., Hay, B., Hill, S., Holland, S.M., Puck, J.M.

“…Hyper-IgE syndrome (HIES, Job syndrome) is characterized by a triad of elevated IgE, skin abscesses and cyst-forming pneumonia. Non-immunological…”
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Skeletal anomalies in hyper-IgE recurrent infection syndrome (HIES, Job syndrome)1 by CHINEN, J

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