Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Abdul H Siddiqui"'
Autor:
Kasey Andrews, Soheil Meshinchi, Preethi Marri, Abdul H. Siddiqui, Jacek Polski, Arturo Molina, Joseph Chewning, Lisa Eidenschink Brodersen, Chad A. Hudson, Hamayun Imran
Publikováno v:
Blood. 140:11757-11758
Publikováno v:
Journal of pediatric hematology/oncology. 42(7)
The management of ovarian immature teratoma (IT) presents several challenges. It occurs both in children and adults and therefore is managed by pediatric oncologists as well as adult and gynecologic oncologists. Treatment approach; however, varies si
Autor:
Abdul H. Siddiqui, Archana M. Agarwal, Robert D. Christensen, Hassan M. Yaish, Roberto Nussenzveig
Publikováno v:
Neonatology. 106:140-142
We report a neonate with early and severe hemolytic jaundice and low erythrocyte pyruvate kinase enzymatic activity (PKLR mutation (c.1573delT) with an erythrocyte PK activity of 6.2 U/g hemoglobin. Her asymptomatic father was heterozygous for the co
Autor:
Peter B. Soh, Abdul H. Siddiqui
Publikováno v:
Pediatric hematology and oncology. 32(4)
The study assessed changes in cerebral blood flow and need for chronic blood transfusions in sickle cell disease children after splenectomy. A retrospective chart review of 40 children splenectomized between 1999 and 2014 was performed. The mean time
Publikováno v:
World Journal of Hepatology
Autoimmune hepatitis (AIH) is a progressive liver disease that is often associated with extrahepatic autoimmune disorders. Evans syndrome (ES) is a rare autoimmune disorder, which is characterized by immune thrombocytopenia and autoimmune hemolytic a
Autor:
Hassan M, Yaish, Roberto H, Nussenzveig, Archana M, Agarwal, Abdul H, Siddiqui, Robert D, Christensen
Publikováno v:
Neonatology. 106(2)
We report a neonate with early and severe hemolytic jaundice and low erythrocyte pyruvate kinase enzymatic activity (2 U/g hemoglobin, reference interval 9-22). We found her asymptomatic mother to be heterozygous for a novel PKLR mutation (c.1573delT
Publikováno v:
Blood. 128:3799-3799
INTRODUCTION: Patients with hemophilia are prone to life threatening bleeds and central line associated morbidities. It is pivotal that emergency departments (ED) are both equipped and trained to address these complications with acuity. The purpose o
Publikováno v:
Pediatric hematology and oncology. 30(5)
We performed a retrospective chart review of children with sickle cell disease hospitalized for fever at our local institution. We reviewed 456 hospitalizations in 133 patients between January 2006 and June 2012. The prevalence of true bacteremia was
Publikováno v:
Pediatric hematology and oncology. 30(3)
Mucormycosis is a rare, but invasive infection caused by ubiquitous molds. Amphotericin B and surgery have been known to help improve the outcome. Sporadic case reports support the use of posaconazole in adults. We report a toddler with acute lymphob
Publikováno v:
Blood. 126:1101-1101
Introduction Von Willebrand's disease (VWD) is the most common inherited bleeding disorder. It is characterized by both quantitative and qualitative defects of the von Willebrand Factor (VWF) and generally manifests as menorrhagia, epistaxis and easy