Zobrazeno 1 - 10 of 94 pro vyhledávání: '"F. A. Oski"'
1
Henna: a potential cause of oxidative hemolysis and neonatal hyperbilirubinemia
Autor: W H, Zinkham, F A, Oski
Publikováno v: Pediatrics. 97(5)
To evaluate the in vitro oxidation potential of lawsone (2-hydroxy-1,4 naphthoquinone). Lawsone is a chemical present in henna, the crushed leaves of which are used worldwide as a cosmetic agent to stain the hair, skin, and nails.Venous blood from gl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::715f7a8b6a15cf3df97780f12cafdb3a
https://pubmed.ncbi.nlm.nih.gov/8628611
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3
Office pediatrics. Physical growth and general nutrition
Autor: F A, Oski
Publikováno v: Current opinion in pediatrics. 7(3)
Obesity is now one of the most prevalent diseases in the US population. Many observations suggest that two and possibly three critical periods exist for the development of obesity and its complications. An expert committee has developed guidelines fo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d7dca95f663e6bc37a1419ef001a350a
https://pubmed.ncbi.nlm.nih.gov/7663625
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7
Syndrome of recurrent increased secretion of antidiuretic hormone following multiple doses of vincristine
Autor: M J, Stuart, C, Cuaso, M, Miller, F A, Oski
Publikováno v: Blood. 45:315-320
The syndrome of inappropriate antidiuretic hormone secretion (SIADH) has been recognized to occur following treatment with vincristine. None of the reports have provided information regarding its potential for recurrence on further challenge with vin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::129a0436e05869008d6c7f872b511eee
https://doi.org/10.1182/blood.v45.3.315.bloodjournal453315
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8
Hereditary Hemolytic Anemia with Hexokinase Deficiency
Autor: J L Naiman, Arthur S. Schneider, Donald E. Paglia, F A Oski, William N. Valentine, Marjorie A. Baughan
Publikováno v: New England Journal of Medicine. 276:1-11
IT is now clear that hereditary hemolytic anemias not associated with hemoglobinopathy or with the thalassemia syndromes are frequently due to inherited deficiencies in one or another of the enzymes upon which the erythrocyte is dependent to meet its
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d4beec413f0a17cb30a1910cfb851b
https://doi.org/10.1056/nejm196701052760101
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