Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alice Bisbee"'
Autor:
David M. Johnson, Geoffrey T. Gibney, Shau Yin Ha, Yu-Lung Lau, Lindsay A. Farrer, Edmond S. K. Ma, Acw Lee, Carolien I.M. Panhuysen, Jason C. C. So, David H.K. Chui, Hui Leung Yuen, Li Chong Chan, Martin H. Steinberg, Chi Kong Li, John J. Farrell, Alice Bisbee, Chi Keung Li
Publikováno v:
American Journal of Hematology. 83:458-464
Enhanced fetal hemoglobin (Hb F) production can partially compensate for the lack of adult hemoglobin (Hb A) in patients with β-thalassemia major or intermedia, and ameliorate the clinical severity of these diseases. To further elucidate factors gov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86aed41a9c8c103f0c67fbd1271e2ba3
https://doi.org/10.1002/ajh.21150
https://doi.org/10.1002/ajh.21150
Autor:
Colin D. Marchant, Bingxia Wang, Timothy Heeren, Stephen I. Pelton, Howard Bauchner, Alice Bisbee, Megan McCabe
Publikováno v:
Pediatrics. 117:1009-1017
OBJECTIVES. To determine whether we could increase adherence to the Centers for Disease Control and Prevention (CDC) recommendations with well-accepted approaches to improving quality of care and adherence to the CDC recommendations resulted in impro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1394ae38805932d4f98c12e38c715d69
https://doi.org/10.1542/peds.2005-2172
https://doi.org/10.1542/peds.2005-2172
Autor:
Diego F. Wyszynski, Martin H. Steinberg, Alice Bisbee, Vikki G. Nolan, Lindsay A. Farrer, John J. Farrell, Stephen H. Embury, Clinton T. Baldwin, Qianli Ma, Yvonne Amirault
Publikováno v:
British Journal of Haematology. 128:266-272
The complications of sickle cell disease are probably determined by genes whose products modify the pathophysiology initiated by the sickle haemoglobin mutation. Priapism, one vaso-occlusive manifestation of sickle cell disease, affects more than 30%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c0c7ec949f2ffdede5c8c5e81091399
https://doi.org/10.1111/j.1365-2141.2004.05295.x
https://doi.org/10.1111/j.1365-2141.2004.05295.x
Publikováno v:
Archives of Physical Medicine and Rehabilitation. 80:1450-1456
Objective: To present preliminary data on the health-related consequences for people with spinal cord injury (SCI) of participation in a prepaid, risk-based, managed care plan. Design: Baseline data from a longitudinal interview survey. Setting: Mass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc345e63cf224d5cb5776dac6e5274c6
https://doi.org/10.1016/s0003-9993(99)90257-5
https://doi.org/10.1016/s0003-9993(99)90257-5
Autor:
John L. Berk, Giampaolo Merlini, Michael A. Heneghan, Ole B. Suhr, Yukio Ando, Taro Yamashita, Alice Bisbee, Laura Obici, Peter J. Dyck, Yoshiki Sekijima, Jeffrey W. Kelly, Shu-ichi Ikeda, Peter D. Gorevic, Martha Skinner, Steven R. Zeldenrust
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 19
Familial amyloidotic polyneuropathy (FAP) is a protein folding disorder that induces neuropathy and cardiomyopathy, leading to death within 7-15 years after onset of clinical disease. In vitro, small ligands binding the thyroid hormone docking site s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a0e35496b8552d77176f829df574dcd
https://pubmed.ncbi.nlm.nih.gov/22551208
https://pubmed.ncbi.nlm.nih.gov/22551208
Autor:
Paola Sebastiani, Stephen H. Embury, Lindsay A. Farrer, Diego F. Wyszynski, Vikki G. Nolan, John J. Farrell, Alice Bisbee, Martin H. Steinberg, Clinton T. Baldwin, Qianli Ma
In patients with sickle cell disease, clinical complications including osteonecrosis can vary in frequency and severity, presumably due to the effects of genes that modify the pathophysiology initiated by the sickle mutation. Here, we examined the as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00070747a7e6305d5cc173511b723c6c
https://europepmc.org/articles/PMC1895132/
https://europepmc.org/articles/PMC1895132/
Publikováno v:
Pediatrics. 115(5)
Background. E-mail exchange between parents of patients and providers has been cited by the Institute of Medicine as an important aspect of contemporary medicine; however, we are unaware of any data describing actual exchanges. Objective. The purpose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96143782f905f6fc07870db2f6dae9ce
https://pubmed.ncbi.nlm.nih.gov/15867036
https://pubmed.ncbi.nlm.nih.gov/15867036
Autor:
Shu-ichi Ikeda, Theodore Colton, Erik Nordh, Janice F. Wiesman, Peter J. Dyck, Jeffery W. Kelly, John L. Berk, Alice Bisbee, Steven R. Zeldenrust, Michael A. Heneghan, Denis Rybin, Yukio Ando, Manuel Corato, Giampaolo Merlini, William J. Litchy, Taro Yamashita, Alessandro Lozza, Peter D. Gorevic, Martha Skinner, Laura Obici, Ole B. Suhr, David C. Seldin, Yoshiki Sekijima, Jessica Robinson-Papp, Andrea Cortese
Publikováno v:
JAMA. 310:2658
Familial amyloid polyneuropathy, a lethal genetic disease caused by aggregation of variant transthyretin, induces progressive peripheral nerve deficits and disability. Diflunisal, a nonsteroidal anti-inflammatory agent, stabilizes transthyretin tetra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4002760b26d4924bb69d02bd2b27ab3c
https://doi.org/10.1001/jama.2013.283815
https://doi.org/10.1001/jama.2013.283815
Autor:
Vikki G. Nolan, Diego F. Wyszynski, Clinton T. Baldwin, Qianli Ma, Martin H. Steinberg, Lindsay A. Farrer, John J. Farrell, Adeboye H. Adewoye, Matt Fourcade, Alice Bisbee
Publikováno v:
Blood. 106:2317-2317
Sickle cell disease patients have a high risk of developing leg ulcers. In the CSSCD database we found 378 patients with a confirmed history of leg ulcers and chose 920 patients without ulcers to serve as controls. α Thalassemia reduces hemolysis in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9f4d23bab6be248e0dcedaf4d3112bc
https://doi.org/10.1182/blood.v106.11.2317.2317
https://doi.org/10.1182/blood.v106.11.2317.2317
Autor:
Qianli Ma, Erica P. Homan, Diego F. Wyszynski, Clinton T. Baldwin, John J. Farrell, Vikki G. Nolan, Martin H. Steinberg, Lindsay A. Farrer, Paola Sebastiani, Adeboye H. Adewoye, Alice Bisbee
Publikováno v:
Blood. 106:3170-3170
Patients with sickle cell disease have an increased risk of bacteremia. To study the genetic basis for this increased susceptibility we studied the association of single nucleotide polymorphisms (SNPs) in candidate genes that might affect the risk of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90f068e2b648041a8694f125b804af7f
https://doi.org/10.1182/blood.v106.11.3170.3170
https://doi.org/10.1182/blood.v106.11.3170.3170