Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Thomas F. Necheles"'
Autor:
Thomas F. Necheles, Carol Crowley
Publikováno v:
Clinics in Perinatology. 3:161-175
Diagnosis and management of the most common hereditary disorders of the erythrocyte are discussed. These congenital defects may continue to present problems through infancy and childhood. These problems may be anticipated and ameliorated or prevented
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0904033a3d2f746bfae7bae8622a3b4c
https://doi.org/10.1016/s0095-5108(18)31279-x
https://doi.org/10.1016/s0095-5108(18)31279-x
Autor:
Bahman Emami, Henry H. Banks, Won H. Oh, Jorge C. Paradelo, Thomas F. Necheles, Ivanka Tchakarova, John E. Munzenrider
Publikováno v:
Radiology. 125:497-502
The rationale for prebiopsy and preoperative irradiation in a multimodal approach to treatment of osteosarcoma is presented. Six patients with osteosarcoma underwent preoperative irradiation, amputation, and elective chemotherapy. Five of these also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04d38ef147b081aae1fe9573be9c17f8
https://doi.org/10.1148/125.2.497
https://doi.org/10.1148/125.2.497
Publikováno v:
New England Journal of Medicine. 291:1351-1355
Presentation of Case A 12-month-old girl was admitted to the hospital because of a thoracoabdominal mass. She was born of a normal pregnancy, labor and delivery and was well until three months before admission, when she began to have diarrhea after e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b61f30f84b8adbb2e79b31da8f009617
https://doi.org/10.1056/nejm197412192912511
https://doi.org/10.1056/nejm197412192912511
Publikováno v:
Acta Paediatrica. 65:361-367
Carboxyhaemoglobin levels were measured in 250 consecutive, normal, term newborns and in a group of 75 severely jaundiced infants in an effort to assess the role of haemolysis in non-specific neonatal hyperbilirubinaemia--"Physiologic jaundice"-as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d0c28a9ddca69c4469858bb6226bad0
https://doi.org/10.1111/j.1651-2227.1976.tb04898.x
https://doi.org/10.1111/j.1651-2227.1976.tb04898.x
Autor:
Donald M. Allen, Thomas F. Necheles
Publikováno v:
New England Journal of Medicine. 280:203-206
THE "Heinz-body anemias" are a group of hemolytic syndromes of diverse etiology with a common morphologic characteristic, first described by Heinz,1 of one or more inclusion bodies within affected ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ed79769c8e46b06ca2db69f7e6286e7
https://doi.org/10.1056/nejm196901232800406
https://doi.org/10.1056/nejm196901232800406
Publikováno v:
Blood. 28:501-512
1. Three siblings with Hb H thalassemia disease have been observed in a family in which 17 members from 3 generations have been examined. Four additional family members have α-thalassemia minor. 2. A genetic examination of the family provides furthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f80b01c21b18314fb15ea09c4151752
https://doi.org/10.1182/blood.v28.4.501.501
https://doi.org/10.1182/blood.v28.4.501.501
Publikováno v:
The American Journal of Medicine. 49:125-132
A new variant of glucose-6-phosphate dehydrogenase (G-6-PD), G-6-PD Worcester, is described in a Caucasian family with associated congenital, nonspherocytic hemolytic anemia, absent erythrocyte G-6-PD activity and optic atrophy. The inheritance of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e4ba3852ddc0aad8ce9b81e5e8f1924
https://doi.org/10.1016/s0002-9343(70)80122-x
https://doi.org/10.1016/s0002-9343(70)80122-x
Publikováno v:
The Journal of Pediatrics. 72:319-324
A genetically determined partial deficiency of the erythrocyte enzyme glutathioneperoxidase has been found in 4 unrelated newborn infants. This partial enzyme deficiency was found associated with a syndrome characterized by hyperbilirubinemia, increa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8a45685a9a3edbc4fd12e2cc06cd8f7
https://doi.org/10.1016/s0022-3476(68)80202-1
https://doi.org/10.1016/s0022-3476(68)80202-1
Publikováno v:
The American Journal of Medicine. 50:542-546
Defects of the hexosemonophosphate shunt-glutathione (HMP-GSH) pathways of the erythrocyte may lead to oxidative denaturation of hemoglobin and cell stroma with resulting hemolysis. The administration of oxidant drugs to subjects with such lesions pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85890720cb8fec8e53b5040db8d6cacf
https://doi.org/10.1016/0002-9343(71)90343-3
https://doi.org/10.1016/0002-9343(71)90343-3
Autor:
William Dameshek, Thomas F. Necheles
Publikováno v:
Blood. 29:550-553
The in vitro synthesis of heme and globin has been studied in bone marrow cell suspensions obtained from five patients with Di Guglielmo syndrome. In all, a defect of heme synthesis was demonstrated, but globin synthesis was greatly reduced in only t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25121e480c26473614ade58e8c784ea3
https://doi.org/10.1182/blood.v29.4.550.550
https://doi.org/10.1182/blood.v29.4.550.550