Zobrazeno 1 - 10
of 42
pro vyhledávání: '"J A, Stolz"'
Autor:
Elizabeth R Gunn, Jacquelyn M. Powers, AKM Fazlur Rahman, Christina J. Bemrich-Stolz, Stephen Mennemeyer, Jeffrey D. Lebensburger, Hope P. Wilson
Publikováno v:
Blood. 140:1219-1220
Autor:
Dakshin Padmanabhan, Elizabeth R Gunn, Christina J. Bemrich-Stolz, Jeffrey D. Lebensburger, Wendy Landier
Publikováno v:
Blood. 140:5137-5138
Autor:
Jeffrey D. Lebensburger, David McCall, Hope P. Wilson, Lee Hilliard, Christina J. Bemrich-Stolz, Thomas H. Howard, Prasannalaxmi Palabindela, Vishnu Nagalapuram
Publikováno v:
Pediatrics. 146(4)
BACKGROUND: Children with isolated neutropenia (absolute neutrophil count [ANC] METHODS: We performed a 5.5-year institutional review board–approved retrospective chart review of children referred to our pediatric hematology and oncology clinics fo
Autor:
Charles Schlappi, Jeffrey D. Lebensburger, Lee Hilliard, Prasannalaxmi Palabindela, Christina J. Bemrich-Stolz, Thomas H. Howard, Varsha Kulkarni
Publikováno v:
Pediatrics. 142
OBJECTIVES: Incidental isolated mild to moderate thrombocytopenia is a frequent laboratory finding prompting a referral to pediatric hematology-oncology. We tested the hypothesis that patients with isolated asymptomatic mild thrombocytopenia would no
Autor:
Lee Hilliard, Thomas H. Howard, Christina J. Bemrich-Stolz, Jeffrey D. Lebensburger, Jewell H. Halanych
Publikováno v:
International Journal of Hematology and Therapy. 1:1-6
Background Young adults with sickle cell anemia are at high risk for increased hospitalization and death at the time of transition to adult care. This may be related to failure of the transition system to prepare young adults for the adult healthcare
Publikováno v:
NPG Neurologie - Psychiatrie - Gériatrie. 13:107-116
Resume Les troubles de la deglutition peuvent etre causes par de nombreuses pathologies neurologiques, œsophagiennes, oto-rhino-laryngologiques (ORL) ou encore etre d’origine iatrogene. Leur presentation clinique est souvent insidieuse et peu spec
Autor:
Bisakha Sen, Thomas H. Howard, Emily Waite, Varsha Kulkarni, Jeffrey D. Lebensburger, Lee Hilliard, Amanda M. Brandow, Cathy Caldwell, Christina J. Bemrich-Stolz
Publikováno v:
Pediatric Blood & Cancer. 65:e27423
Background Recurrent pain events or chronic pain are among the most common complications of sickle cell disease. Despite attempts to maximize adherence to and dosing of hydroxyurea, some patients continue to suffer from pain. Our institution develope
Autor:
Rakeshkumar J Patel, Thomas H. Howard, Jeffrey D. Lebensburger, Lee Hilliard, Prasannalaxmi Palabindela, Christina J. Bemrich-Stolz
Publikováno v:
Journal of Blood Medicine
Jeffrey D Lebensburger, Rakeshkumar J Patel, Prasannalaxmi Palabindela, Christina J Bemrich-Stolz, Thomas H Howard, Lee M HilliardDivision of Pediatric Hematology Oncology, University of Alabama at Birmingham, Birmingham, AL, USAPurpose: Patients wit
Autor:
Reed A. Dimmitt, W. Winn Chatham, Claudia Bracaglia, Fabrizio De Benedetti, Mark R. Walter, Hao Li, Kejian Zhang, Randall Q. Cron, Mingce Zhang, Christina J. Bemrich-Stolz, Giusi Prencipe, Timothy Beukelman, Alexei A. Grom
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 196(6)
Frequently fatal, primary hemophagocytic lymphohistiocytosis (HLH) occurs in infancy resulting from homozygous mutations in NK and CD8 T cell cytolytic pathway genes. Secondary HLH presents after infancy and may be associated with heterozygous mutati
Autor:
James M. Johnston, Christina J. Bemrich-Stolz, Thomas H. Howard, Winfield S. Fisher, Lee Hilliard, Jeffrey D. Lebensburger, Michelle H. Chua, Christoph J. Griessenauer
Publikováno v:
Journal of neurosurgery. Pediatrics. 16(1)
OBJECT Pediatric patients with sickle cell disease (SCD) and moyamoya syndrome (MMS) are at significant risk for cerebrovascular accidents despite chronic transfusion therapy. Encephaloduroarteriosynangiosis (EDAS) and encephalomyoarteriosynangiosis