Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Richard Drachtman"'
Autor:
Biree Andemariam, Modupe Idowu, Nirmish Shah, Richard Drachtman, Archana Sharma, Alexander Glaros, Maureen Achebe, Alecia Nero, Brooke Hayward, Michelle Xu, Susanna Curtis
Publikováno v:
HemaSphere, Vol 7, p e139426f (2023)
Externí odkaz:
https://doaj.org/article/a657dd6d2aee4ef1885c26be62ee3e52
Publikováno v:
Cancer Medicine, Vol 10, Iss 4, Pp 1327-1334 (2021)
Abstract Background The purpose of this study was to examine the factors associated with disparities in overall survival (OS) by race in pediatric diffuse large B‐cell lymphoma (DLBCL) patients. Methods We evaluated clinical features and survival a
Externí odkaz:
https://doaj.org/article/4d423af94cf84bb5bf451977d61a9296
Autor:
Andrew S. Kopecky, PhD, Atif J. Khan, MD, Wilbur Pan, MD, Richard Drachtman, MD, Rahul R. Parikh, MD
Publikováno v:
Advances in Radiation Oncology, Vol 2, Iss 4, Pp 588-596 (2017)
Purpose: We examined national outcomes and patterns of care for pediatric patients with medulloblastoma (MB) in a large observational cohort. Methods and materials: Using the National Cancer Database, we evaluated the clinical features and survival o
Externí odkaz:
https://doaj.org/article/7739d1aa22944019a9f98a5c5c946071
Publikováno v:
Pediatric Blood & Cancer. 69
Autor:
Bridget L, Findlay, Brian M, Shinder, Aisha, Fatima, Evita, Sadimin, Richard, Drachtman, Rahul R, Parikh, Eric A, Singer
Publikováno v:
Journal of renal cancer. 2(1)
Primary Ewing sarcoma of the kidney is an extremely rare and aggressive tumor affecting young adults. We present the case of a 22-year-old male with primary Ewing sarcoma/primitive neuroectodermal tumor (EWS/PNET) of the kidney who underwent right ra
Autor:
Bridget L Findlay, Brian M Shinder, Aisha Fatima, Evita Sadimin, Richard Drachtman, Rahul R Parikh, Eric A Singer
Publikováno v:
Journal of Renal Cancer. 2
Publikováno v:
Pediatric bloodcancer. 55(4)
Thyroid carcinomas are an uncommon entity in childhood. We report a case of papillary thyroid cancer presenting as Horner syndrome in a 14 year-old child, which is the only reported such case in the pediatric population.
Publikováno v:
Acta Paediatrica. 79:990-993
Two siblings with congenital neurologic structural anomalies and delayed-onset selective bone marrow hypoplasia in a previously undescribed constellation of symptoms are presented. Differences between these cases and other well known syndromes are di