Zobrazeno 1 - 10
of 228
pro vyhledávání: '"Yaddanapudi Ravindranath"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 4, Pp 244-249 (2024)
Sickle cell disease (SCD) was first described in 1910 in African Americans, and the mutant hemoglobin S (HbS) was identified by electrophoresis in 1948. Sickle cell disease is the first genetic disease to be molecularly defined - a single point mutat
Externí odkaz:
https://doaj.org/article/b0011bb07b7646f182e8cd1ab3d3e14c
Autor:
Ahmar Urooj Zaidi, Steven Buck, Manisha Gadgeel, Miguel Herrera-Martinez, Araathi Mohan, Kenya Johnson, Shruti Bagla, Robert M. Johnson, Yaddanapudi Ravindranath
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
The measurement of band 3 (AE1, SLC4A1, CD233) content of red cells by eosin-5- maleimide (EMA) staining is swiftly replacing conventional osmotic fragility (OF) test as a tool for laboratory confirmation of hereditary spherocytosis across the globe.
Externí odkaz:
https://doaj.org/article/bdac5d7b497d4c2b84330df110beb8d8
Autor:
Shruti Bagla, Kanta Bhambhani, Manisha Gadgeel, Steven Buck, Jian-Ping Jin, Yaddanapudi Ravindranath
Publikováno v:
Haematologica, Vol 104, Iss 9 (2019)
Externí odkaz:
https://doaj.org/article/998d791c3e134ea5b36faa0ebfd19ce8
Autor:
Eduard J. van Beers, Stephanie van Straaten, D. Holmes Morton, Wilma Barcellini, Stefan W. Eber, Bertil Glader, Hassan M. Yaish, Satheesh Chonat, Janet L. Kwiatkowski, Jennifer A. Rothman, Mukta Sharma, Ellis J. Neufeld, Sujit Sheth, Jenny M. Despotovic, Nina Kollmar, Dagmar Pospíšilová, Christine M. Knoll, Kevin Kuo, Yves D. Pastore, Alexis A. Thompson, Peter E. Newburger, Yaddanapudi Ravindranath, Winfred C. Wang, Marcin W. Wlodarski, Heng Wang, Susanne Holzhauer, Vicky R. Breakey, Madeleine Verhovsek, Joachim Kunz, Melissa A. McNaull, Melissa J. Rose, Heather A. Bradeen, Kathryn Addonizio, Anran Li, Hasan Al-Sayegh, Wendy B. London, Rachael F. Grace
Publikováno v:
Haematologica, Vol 104, Iss 2 (2019)
Externí odkaz:
https://doaj.org/article/7c186564490a4bcea73e25b735945c6c
Autor:
Aman Wadhwa, Yanjun Chen, Lindsey Hageman, Anna Hoppmann, Anne Angiolillo, David Dickens, Joseph P Neglia, Yaddanapudi Ravindranath, Kim Ritchey, Amanda Termuhlen, F. Lennie Wong, Wendy Landier, Smita Bhatia
Publikováno v:
Blood Journal.
The association between individual-level poverty and relapse in children receiving maintenance treatment for acute lymphoblastic leukemia (ALL) remains unclear. In a secondary analysis of COG-AALL03N1, we used data from US Census Bureau to categorize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80dec472677a01837769cbf1892ae65a
https://doi.org/10.1182/blood.2023019631
https://doi.org/10.1182/blood.2023019631
Autor:
Jennifer M. Geris, Mark R. Schleiss, Anthony J. Hooten, Erica Langer, Nelmary Hernandez-Alvarado, Michelle A. Roesler, Jeannette Sample, Lindsay A. Williams, David S. Dickens, Rajen J. Mody, Yaddanapudi Ravindranath, Kate L. Gowans, Matthew G. Pridgeon, Logan G. Spector, Heather H. Nelson
Publikováno v:
JAMA network open. 6(1)
ImportanceAcute lymphoblastic leukemia (ALL) is the most common form of pediatric cancer, and a leading cause of death in children. Understanding the causes of pediatric ALL is necessary to enable early detection and prevention; congenital cytomegalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aaf7403557bae35024a42dbbd1ce7d0
https://pubmed.ncbi.nlm.nih.gov/36622672
https://pubmed.ncbi.nlm.nih.gov/36622672
Autor:
Aman Wadhwa, Yanjun Chen, Lindsey Hageman, Anna L. Hoppmann, Anne Angiolillo, David S. Dickens, Glen Lew, Joseph P. Neglia, Yaddanapudi Ravindranath, A. Kim Ritchey, Amanda Termuhlen, F. Lennie Wong, Wendy Landier, Smita Bhatia
Publikováno v:
CancerREFERENCES. 129(1)
Obesity at diagnosis of childhood acute lymphoblastic leukemia (ALL) is associated with greater risk of relapse; whether this association extends to obesity during maintenance is unstudied.This study used data from AALL03N1 to calculate median body m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::792388120b9a157131873a80c4830009
https://pubmed.ncbi.nlm.nih.gov/36369905
https://pubmed.ncbi.nlm.nih.gov/36369905
Autor:
Jeffrey W. Taub, Batool Al‐Qanber, Süreyya Savaşan, Yaddanapudi Ravindranath, Steven Buck, Manisha Gadgeel
Publikováno v:
Annals of Hematology. 100:1695-1700
Children with Down syndrome (DS) are at an increased risk of developing transient abnormal myelopoiesis (TAM) and acute leukemia. Aberrant expression of CD56 has been observed on myeloid leukemic blasts in DS patients. In general, CD56 expression in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a297f33741a0a0db77873dc7e73c128
https://doi.org/10.1007/s00277-021-04531-x
https://doi.org/10.1007/s00277-021-04531-x
Autor:
Aman Wadhwa, Yanjun Chen, Lindsey Hageman, Anna Hoppmann, Anne L Angiolillo, David Dickens, Glen Lew, Joseph P. Neglia, Yaddanapudi Ravindranath, Arthur K. Ritchey, Amanda Muench Termuhlen, Lennie Wong, Wendy Landier, Smita Bhatia
Publikováno v:
Blood. 140:2183-2184
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56a0268691937fe71de803582350a4fe
https://doi.org/10.1182/blood-2022-163271
https://doi.org/10.1182/blood-2022-163271
Autor:
Ahmar U. Zaidi, Steven Buck, Michael Chicka, Katherine Regling, Yaddanapudi Ravindranath, Meera Chitlur, Shruti Bagla, Leigh Anne Flore, Erin Wakeling, Manisha Gadgeel, Charles A. Schiffer
Publikováno v:
Pediatric Hematology and Oncology. 38:65-79
RUNX1 associated familial platelet disorder (FPD) is a rare autosomal dominant hematologic disorder characterized by thrombocytopenia and/or altered platelet function. There is an increased propensity to develop myeloid malignancy (MM) - acute myeloi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1957c08ca4204299fdfc5df30535355
https://doi.org/10.1080/08880018.2020.1814463
https://doi.org/10.1080/08880018.2020.1814463