Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Arun R Panigrahi"'
Autor:
Ross M. Perry, Scott D. Casey, Alex Q. Lee, Sylvia P. Bowditch, Mary A. Rasmussen, Viyeka Sethi, Arun R. Panigrahi
Publikováno v:
Case Reports in Pediatrics, Vol 2024 (2024)
In this article, we describe a novel case of SARS-CoV-2-associated-hemophagocytic lymphohistiocytosis (HLH) complicated by posterior reversible encephalopathy syndrome (PRES). Initially diagnosed with multisystem inflammatory response in children (MI
Externí odkaz:
https://doaj.org/article/4948062e8f7c4bf49cec07ee289aa8e6
Publikováno v:
The American Journal of Emergency Medicine. 59:217.e1-217.e3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4ddd09b6d883274fff3207cab9397eb
https://doi.org/10.1016/j.ajem.2022.06.024
https://doi.org/10.1016/j.ajem.2022.06.024
Autor:
Jason E. Farrar, Anupama Narla, Kelly Walkovich, Helge Hartung, Grzegorz Nalepa, Adrianna Vlachos, Evangelia Atsidaftos, Jeffrey M. Lipton, Mohammad Lutfi Lababidi, Jonathan Bernstein, Ellen Muir, Zora R. Rogers, Thomas W. Loew, Waseem Alhushki, Colin A. Sieff, Bertil Glader, Barbara Gruner, Christine M. Knoll, Arun R Panigrahi
Publikováno v:
Pediatr Blood Cancer
Background Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, short stature, congenital anomalies, and cancer predisposition. Most cases are due to mutations in genes encoding ribosomal proteins (RP) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f35da0422ca685604b2d6c0cfaafb63
https://europepmc.org/articles/PMC8273758/
https://europepmc.org/articles/PMC8273758/
Publikováno v:
Pediatric Blood & Cancer. 64:287-293
Background Successful treatment of both pediatric autoimmune hemolytic anemia (AIHA) and immune thrombocytopenic purpura (ITP), specifically those that are refractory to first-line therapies, remains unsatisfactory in terms of long-term remission and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e11d381b4af4271a2136679300287dae
https://doi.org/10.1002/pbc.26210
https://doi.org/10.1002/pbc.26210
Autor:
Salvatore Bertolone, Jennifer Mullinax, Arun R Panigrahi, Ashok Raj, Scott N. Myers, Ryan Eid, John Myers
Publikováno v:
Journal of pediatric hematology/oncology. 38(1)
BACKGROUND Erythrocytapheresis procedures are increasingly used in sickle cell disease. Serum ferritin and noninvasive magnetic resonance imaging measurements of liver iron concentration (LIC) are frequently used to monitor iron overload secondary to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abbfc9d1db5c76c805dbe44719055988
https://pubmed.ncbi.nlm.nih.gov/26650249
https://pubmed.ncbi.nlm.nih.gov/26650249
Autor:
Barbara Gruner, Kelly Walkovich, Christine M. Knoll, Mohammad Lufti Lababidi, Jason E. Farrar, Anupama Narla, Helge Hartung, Zora R. Rogers, Waseem Alhushki, Evangelia Atsidaftos, Ellen Muir, Bertil Glader, Arun R Panigrahi, Colin A. Sieff, Jeffrey M. Lipton, Adrianna Vlachos, Grzegorz Nalepa
Publikováno v:
Blood. 132:755-755
Diamond Blackfan anemia (DBA) is a rare, inherited bone marrow failure syndrome characterized by anemia, congenital anomalies and a predisposition to cancer. The patients usually present during infancy or early childhood, but can also present in adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b29c4e5bf0f45033599eb182f40142b5
https://doi.org/10.1182/blood-2018-99-113570
https://doi.org/10.1182/blood-2018-99-113570
Publikováno v:
Pediatric Blood & Cancer. 66:e27505
Background Delta granule storage pool deficiency (δ-SPD) is a rare platelet disorder in which a deficiency of platelet granules leads to poor aggregation, resulting in varying clinical bleeding phenotypes. Children with δ-SPD have variable laborato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e2cc1147a0535c9cc26a731828116e6
https://doi.org/10.1002/pbc.27505
https://doi.org/10.1002/pbc.27505
Publikováno v:
Children
Children (Basel, Switzerland), vol 5, iss 1
Children (Basel, Switzerland), vol 5, iss 1
Central vein thrombosis as a cause of chylothorax is uncommon, and in a few cases in the literature was related to thrombotic complications of central venous access devices (CVAD). Superior vena cava (SVC) occlusion-induced chylothorax has been descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7076267a73aee1d930b2dc7f9d484a24
https://doi.org/10.3390/children5010007
https://doi.org/10.3390/children5010007
Autor:
Pradeep Padmanabhan, John Myers, Jennifer Mullinax, Arun R Panigrahi, Scott N. Myers, Ashok Raj
Publikováno v:
Blood. 126:2067-2067
Context Early and aggressive use of hydroxyurea (HU) in sickle hemoglobinopathies has been in practice at our comprehensive sickle cell center since 2012 when standardized protocols were still evolving. The consensus treatment protocol for hydroxyure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6217adf06caf18fdb97701bddf680274
https://doi.org/10.1182/blood.v126.23.2067.2067
https://doi.org/10.1182/blood.v126.23.2067.2067
Autor:
Amy Clark, Arun R Panigrahi
Publikováno v:
Blood. 124:2744-2744
Background: Autoimmune cytopenias are defined by immune-mediated destruction of distinct hematopoietic lineages, including white blood cells, red blood cells, and platelets. The destruction of a single lineage in response to an unknown stimulus is kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2590b5d3e60378a388600a7258b9a3d
https://doi.org/10.1182/blood.v124.21.2744.2744
https://doi.org/10.1182/blood.v124.21.2744.2744