Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Timothy L, McCavit"'
Autor:
Leif S. Ludwig, Caleb A. Lareau, Erik L. Bao, Nan Liu, Taiju Utsugisawa, Alex M. Tseng, Samuel A. Myers, Jeffrey M. Verboon, Jacob C. Ulirsch, Wendy Luo, Christoph Muus, Claudia Fiorini, Meagan E. Olive, Christopher M. Vockley, Mathias Munschauer, Abigail Hunter, Hiromi Ogura, Toshiyuki Yamamoto, Hiroko Inada, Shinichiro Nakagawa, Shuichi Ohzono, Vidya Subramanian, Roberto Chiarle, Bertil Glader, Steven A. Carr, Martin J. Aryee, Anshul Kundaje, Stuart H. Orkin, Aviv Regev, Timothy L. McCavit, Hitoshi Kanno, Vijay G. Sankaran
Publikováno v:
Blood
Master regulators, such as the hematopoietic transcription factor (TF) GATA1, play an essential role in orchestrating lineage commitment and differentiation. However, the precise mechanisms by which such TFs regulate transcription through interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef5641e60cf7f369f62d5e4aa732d9b7
https://doi.org/10.1182/blood.2021013753
https://doi.org/10.1182/blood.2021013753
Autor:
Sandeep K. Rajan, Linda G. Shaffer, Timothy L. McCavit, Miguel A. Escobar, Novinyo S. Amega, Mark Holguin
Publikováno v:
Haemophilia. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc2de20564770172efc093dc0ea25eeb
https://doi.org/10.1111/hae.14175
https://doi.org/10.1111/hae.14175
Autor:
Jason Y. Park, Charles F. Timmons, Dania D. Lopez, Hung S. Luu, Midori Mitui, Timothy L. McCavit
Publikováno v:
Hemoglobin. 43:204-206
We describe Hb Alcorn County, a heterozygous hemoglobin (Hb) variant, in a 6-month-old Hispanic male and his mother. DNA sequencing demonstrated a mutation on the HBB gene [β40(C6)Arg→Thr; HBB: c.122G>C (p.Arg41Thr)], predictive of a substitution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::544153e1aa2a3106bd4f5fabb3b4796e
https://doi.org/10.1080/03630269.2019.1649279
https://doi.org/10.1080/03630269.2019.1649279
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 30:247-250
Study Objective To assess the clinical severity and initial treatment of iron deficiency anemia (IDA) in female adolescents with heavy menstrual bleeding (HMB) in our center. Design Retrospective cohort study of electronic medical records via search
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::410f9d079a54ed4ba7e018d6f13ddec3
https://doi.org/10.1016/j.jpag.2016.10.010
https://doi.org/10.1016/j.jpag.2016.10.010
Autor:
Hung S, Luu, Timothy L, McCavit, Jason Y, Park, Midori, Mitui, Dania D, Lopez, Charles F, Timmons
Publikováno v:
Hemoglobin. 43(3)
We describe Hb Alcorn County, a heterozygous hemoglobin (Hb) variant, in a 6-month-old Hispanic male and his mother. DNA sequencing demonstrated a mutation on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::90a7ab713fa0a492ea260cdb7c6349cd
https://pubmed.ncbi.nlm.nih.gov/31397596
https://pubmed.ncbi.nlm.nih.gov/31397596
Publikováno v:
Journal of Pediatric Hematology/Oncology. 37:402-405
Infantile myofibromatosis (IM) is most commonly limited to cutaneous lesions that resolve spontaneously. However, generalized IM with visceral involvement, which has a reported mortality rate as high as 73%, has been successfully treated with a combi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93793ad2b78edbb7dc116660e8288c5
https://doi.org/10.1097/mph.0000000000000132
https://doi.org/10.1097/mph.0000000000000132
Autor:
Timothy L. McCavit, Melissa Mathias
Publikováno v:
PEDIATRICS. 135:475-482
BACKGROUND AND OBJECTIVE: Time to opioid administration (TTO) has been suggested as a quality of care measure for sickle cell disease patients with vaso-occlusive crisis (VOC). We sought to determine whether TTO was associated with outcomes of emerge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3406ddc3c0a501fdf92ed0872bb90c
https://doi.org/10.1542/peds.2014-2874
https://doi.org/10.1542/peds.2014-2874
Publikováno v:
Pediatric Blood & Cancer. 62:842-846
Background Iron deficiency anemia (IDA) is the most common hematologic condition in children and adolescents in the United States (US). No prior reports have described the management of IDA by a large cohort of pediatric hematology/oncology specialis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9366f6149ea16ace9cea3d3c2e49861b
https://doi.org/10.1002/pbc.25433
https://doi.org/10.1002/pbc.25433
Publikováno v:
JAMA. 317(22)
Iron-deficiency anemia (IDA) affects millions of persons worldwide, and is associated with impaired neurodevelopment in infants and children. Ferrous sulfate is the most commonly prescribed oral iron despite iron polysaccharide complex possibly being
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e8caa62502b2f69ff9bb58d80b78a42
https://pubmed.ncbi.nlm.nih.gov/28973242
https://pubmed.ncbi.nlm.nih.gov/28973242
Autor:
Mark E. Heiny, Baba Inusa, Michael A. Kraut, Michael J. Noetzel, Natalia Dixon, Rupa Redding-Lallinger, Melanie Kirby-Allen, Sharada A. Sarnaik, Corina E. Gonzalez, Gerald M. Woods, Melissa Rhodes, Janet L. Kwiatkowski, Robert C. McKinstry, Brian Berman, Thomas H. Howard, Emily Riehm Meier, Julie A. Panepinto, William S. Ball, Timothy L. McCavit, Jason Fixler, J. P. Miller, Desirée A. White, Fenella J. Kirkham, Deborah Hirtz, Paul Telfer, James F. Casella, John J. Strouse, Harold P Lehmann, Alexis A. Thompson, Michael R. DeBaun, Karen Kalinyak, Suvankar Majumdar, Annie Kamdem, Allison A. King, Gladstone Airewele, Beng Fuh, Charles T. Quinn, Mae O. Gordon
Publikováno v:
New England Journal of Medicine. 371:699-710
Silent cerebral infarcts are the most common neurologic injury in children with sickle cell anemia and are associated with the recurrence of an infarct (stroke or silent cerebral infarct). We tested the hypothesis that the incidence of the recurrence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9922b2c6c3485f88828914589fabd0f
https://doi.org/10.1056/nejmoa1401731
https://doi.org/10.1056/nejmoa1401731