Zobrazeno 1 - 10
of 394
pro vyhledávání: '"S. Piomelli"'
Publikováno v:
Photodermatology, Photoimmunology & Photomedicine. 11:18-21
Inherited deficiency of ferrochelatase results in erythropoietic protoporphyria (EPP). Genetic heterogeneity at the locus for human ferrochelatase was investigated. Analysis of genomic DNA of patients with EPP and of control subjects by restriction e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0716e92761694b926cda0576062c280f
https://doi.org/10.1111/j.1600-0781.1995.tb00132.x
https://doi.org/10.1111/j.1600-0781.1995.tb00132.x
Publikováno v:
Stroke. 25:2153-2158
Sickle cell disease is associated with cerebral hyperemia, which is therapeutically reduced by transfusion; however, the process of transfusion-induced cerebral perfusion changes has heretofore not been observed. We document the acute changes of intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5252fc14e9608ebecff5983d9b9b4e54
https://doi.org/10.1161/01.str.25.11.2153
https://doi.org/10.1161/01.str.25.11.2153
Publikováno v:
Pediatric Radiology. 25:S122-S124
Deferoxamine chelation therapy (widely used to reduce iron overload in hypertransfused thalassemic patients) has been implicated in causing skeletal growth abnormalities (rachitic-like changes in the long bones and vertebral body flattening), particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e703abaa5fe395653ed67e0461ae8c4
https://doi.org/10.1007/bf03545606
https://doi.org/10.1007/bf03545606
Autor:
S, Piomelli
Publikováno v:
Pediatrics. 93:508-510
Lead is an extremely toxic metal: even a single atom of lead, once in the human body, binds to a protein and induces some damage; the greater the exposure, the more serious the effects. Lead has no physiological function; any amount of body lead refl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0512aa9463e35cd1f29b726c107e94e7
https://doi.org/10.1542/peds.93.3.508
https://doi.org/10.1542/peds.93.3.508
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 7(2)
Four years prior to transplantation, a 14-year-old boy with severe haemophilia A and a high-responding factor VIII (FVIII) inhibitor developed an anteroseptal myocardial infarct while receiving high doses of an activated prothrombin complex concentra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93297113a68457a0d3ea0a9c4a5c84cb
https://pubmed.ncbi.nlm.nih.gov/11260285
https://pubmed.ncbi.nlm.nih.gov/11260285
Autor:
K, Murakami, S, Piomelli
Publikováno v:
Blood. 89(3)
A unique cDNA for hexokinase (HK) was identified from poly(A)+ RNA of human reticulocytes by anchored polymerase chain reaction. This appeared to represent the cDNA for the red blood cell (RBC)-specific HK isozyme (HKR) described in our previous stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4838f957cf9b8db566c03ceea71a621a
https://pubmed.ncbi.nlm.nih.gov/9414310
https://pubmed.ncbi.nlm.nih.gov/9414310
Publikováno v:
Pediatric radiology. 25
Deferoxamine chelation therapy (widely used to reduce iron overload in hypertransfused thalassemic patients) has been implicated in causing skeletal growth abnormalities (rachitic-like changes in the long bones and vertebral body flattening), particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7acfa1699799c8fecf58588fe3a9aec
https://pubmed.ncbi.nlm.nih.gov/8577502
https://pubmed.ncbi.nlm.nih.gov/8577502
Autor:
S, Piomelli
Publikováno v:
Seminars in hematology. 32(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9aed1d0c7191b774ed74ef238eebb974
https://pubmed.ncbi.nlm.nih.gov/8560283
https://pubmed.ncbi.nlm.nih.gov/8560283
Autor:
A. Hurlet, S Piomelli, Walter E. Berdon, Terry L. Levin, Sujit Sheth, S. C. D. Comerci, Carrie Ruzal-Shapiro
Publikováno v:
Pediatric radiology. 25(8)
Magnetic resonance (MR) marrow signal in the axial and appendicular skeleton of 13 transfusion-dependent and chelated pediatric patients with sickle cell anemia (SSD) was compared with marrow signal in six non-transfusion-dependent patients with SSD.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c65043a0114577e6553cc5afd55f74c
https://pubmed.ncbi.nlm.nih.gov/8570314
https://pubmed.ncbi.nlm.nih.gov/8570314
Autor:
Sujit Sheth, Terry L. Levin, Walter E. Berdon, S Piomelli, Carrie Ruzal-Shapiro, Sara J. Abramson
Publikováno v:
Pediatric radiology. 25(8)
The magnetic resonance bone marrow patterns in thalassemia were evaluated to determine changes produced by transfusion and chelation therapy. Thirteen patients had T1- and T2-weighted images of the spine, pelvis and femurs. Three received no therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c08a6f3e65ee974ee9d5342d0bf78f76
https://pubmed.ncbi.nlm.nih.gov/8570313
https://pubmed.ncbi.nlm.nih.gov/8570313