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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d34068aba11f3a1af3444b1f82ee077c
https://doi.org/10.1182/blood-2022-164629
https://doi.org/10.1182/blood-2022-164629
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6735be2b2b4d6881eafc77b0238d43c
https://pubmed.ncbi.nlm.nih.gov/31205224
https://pubmed.ncbi.nlm.nih.gov/31205224
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e608e9ee1ec2a64613011c58d7013a
https://doi.org/10.1159/000363219
https://doi.org/10.1159/000363219
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::224d3644a9eee1997fa92592b1b3d556
https://pubmed.ncbi.nlm.nih.gov/25871740
https://pubmed.ncbi.nlm.nih.gov/25871740
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6515531c8e2505362b379cb502b5bc6
https://doi.org/10.4254/wjh.v9.i23.1008
https://doi.org/10.4254/wjh.v9.i23.1008
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8a9b8fd7953541005d7900cef849ee0
https://pubmed.ncbi.nlm.nih.gov/24969675
https://pubmed.ncbi.nlm.nih.gov/24969675
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd4f7249d099b8570809056bc99ec631
https://doi.org/10.1182/blood.v128.22.3799.3799
https://doi.org/10.1182/blood.v128.22.3799.3799
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7570835cdbe79484935a71694a82529
https://pubmed.ncbi.nlm.nih.gov/23570543
https://pubmed.ncbi.nlm.nih.gov/23570543
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae8409bbe955c5a91f538dc74a741d2
https://pubmed.ncbi.nlm.nih.gov/23444832
https://pubmed.ncbi.nlm.nih.gov/23444832
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6a964e06a15f5d28357f6ec1779871
https://doi.org/10.1182/blood.v126.23.1101.1101
https://doi.org/10.1182/blood.v126.23.1101.1101