Výsledky vyhledávání - "C H, Pegelow"

Homzygous Protein S Deficiency due to a One Base Pair Deletion that Leads to a Stop Codon in Exon III of the Protein S Gene

Autor: C H Pegelow, E. Gómez, P H Reitsma, M R Ledford, Rogier M. Bertina

Publikováno v: Thrombosis and Haemostasis. 71:723-726

SummaryHomozygous protein S (PS) deficiency is a very rare disorder that causes purpura fulminans in affected newborns. This report describes the molecular genetic abnormality of a severe PS deficient child who developed purpura fulminans shortly aft

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::79d541f47b8242c39c470bf89773ca70
https://doi.org/10.1055/s-0038-1642512

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Financial analysis of chronic transfusion for stroke prevention in sickle cell disease

Autor: A S, Wayne, S E, Schoenike, C H, Pegelow

Publikováno v: Blood. 96(7)

Chronic red blood cell transfusion can prevent many of the manifestations of sickle cell disease. The medical costs of chronic transfusion and management of associated side effects, especially iron overload, are considerable. This study was undertake

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::96005240c41f8ddfb927336767d619c2
https://pubmed.ncbi.nlm.nih.gov/11001885

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Cerebrovascular accidents in sickle cell disease: rates and risk factors

Autor: K, Ohene-Frempong, S J, Weiner, L A, Sleeper, S T, Miller, S, Embury, J W, Moohr, D L, Wethers, C H, Pegelow, F M, Gill

Publikováno v: Blood. 91(1)

Cerebrovascular accident (CVA) is a major complication of sickle cell disease. The incidence and mortality of and risk factors for CVA in sickle cell disease patients in the United States have been reported only in small patient samples. The Cooperat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::55cd5c9ee50a9607fc10159111177e61
https://pubmed.ncbi.nlm.nih.gov/9414296

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Influence of penicillin prophylaxis on antimicrobial resistance in nasopharyngeal S. pneumoniae among children with sickle cell anemia. The Ancillary Nasopharyngeal Culture Study of Prophylactic Penicillin Study II

Autor: G M, Woods, J H, Jorgensen, M A, Waclawiw, C, Reid, W, Wang, C H, Pegelow, Z R, Rogers, R V, Iyer, C T, Holbrook, T R, Kinney, E, Vichinsky, M R, DeBaun, N J, Grossman, M D, Thomas, J M, Falletta

Publikováno v: Journal of pediatric hematology/oncology. 19(4)

To evaluate the consequences of prolonged prophylactic penicillin use on the rates of nasopharyngeal colonization with Streptococcus pneumoniae and the prevalence of resistant pneumococcal strains in children with sickle cell anemia.Nasopharyngeal sp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4e902ad97f948e2eff167e2588e320bc
https://pubmed.ncbi.nlm.nih.gov/9256832

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Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease

Autor: F D, Armstrong, R J, Thompson, W, Wang, R, Zimmerman, C H, Pegelow, S, Miller, F, Moser, J, Bello, A, Hurtig, K, Vass

Publikováno v: Pediatrics. 97(6 Pt 1)

Brain magnetic resonance imaging (MRI) and neuropsychological evaluations were conducted to determine whether neuroradiographic evidence of infarct in children with sickle cell disease between ages 6 and 12 years would result in impairment in cogniti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2d3ea3d06c3c7a948de152d3aa0f4e28
https://pubmed.ncbi.nlm.nih.gov/8657528

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The spectrum of brain MR abnormalities in sickle-cell disease: a report from the Cooperative Study of Sickle Cell Disease

Autor: F G, Moser, S T, Miller, J A, Bello, C H, Pegelow, R A, Zimmerman, W C, Wang, K, Ohene-Frempong, A, Schwartz, E P, Vichinsky, D, Gallagher, T R, Kinney

Publikováno v: AJNR Am J Neuroradiol

PURPOSE: To define the spectrum of abnormalities in sickle-cell disease, including infarction, atrophy, and hemorrhage, that are identified by brain MR imaging. METHODS: All MR studies included T1, T2, and intermediate pulse sequences. Images were in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::94b2983eaf6b10e5d27eb9255cbab5b9
https://europepmc.org/articles/PMC8337529/

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Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease

Autor: F M, Gill, L A, Sleeper, S J, Weiner, A K, Brown, R, Bellevue, R, Grover, C H, Pegelow, E, Vichinsky

Publikováno v: Blood. 86(2)

Within the Cooperative Study of Sickle Cell Disease, 694 infants with confirmed sickle cell disease were enrolled at less than 6 months of age. Information about the nature and frequency of complications was collected prospectively over a 10-year per

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::edd5aa8262cf348a0aa3a0ded3e4a1ed
https://pubmed.ncbi.nlm.nih.gov/7492800

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Blood transfusions and immunophenotypic alterations of lymphocyte subsets in sickle cell anemia. The Transfusion Safety Study Group

Autor: W Y, Wong, D R, Powars, E A, Operskalski, J, Hassett, J W, Parker, S, Sarnaik, C H, Pegelow, M W, Hilgartner, C S, Johnson, Y, Zhou

Publikováno v: Blood. 85(8)

Transfusions purportedly induce dysfunction of cell-mediated immunity in sickle cell anemia (SCA). We studied hematologic and lymphocytic indices in 173 human immunodeficiency virus (HIV)-negative subjects with SCA and 131 black controls. Children ag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc48515f9da8533f7c86c30632ff1801
https://pubmed.ncbi.nlm.nih.gov/7718880

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Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene

Autor: E, Gómez, M R, Ledford, C H, Pegelow, P H, Reitsma, R M, Bertina

Publikováno v: Thrombosis and haemostasis. 71(6)

Homozygous protein S (PS) deficiency is a very rare disorder that causes purpura fulminans in affected newborns. This report describes the molecular genetic abnormality of a severe PS deficient child who developed purpura fulminans shortly after birt

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4b75d7d38d5dc5cd88c668c982214726
https://pubmed.ncbi.nlm.nih.gov/7974339

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