Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Harriet G. Guild"'
Publikováno v:
Archives of disease in childhood. 10(58)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd2b45b234fb17cb602c4f18844a718e
https://pubmed.ncbi.nlm.nih.gov/21032001
https://pubmed.ncbi.nlm.nih.gov/21032001
Autor:
C. Bernard Brack, Harriet G. Guild
Publikováno v:
American Journal of Obstetrics and Gynecology. 76:1105-1113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab736523311d8776ddd7b7d02b3d339
https://doi.org/10.1016/0002-9378(58)90191-1
https://doi.org/10.1016/0002-9378(58)90191-1
Publikováno v:
The American Journal of Medicine. 22:636-652
1.1. Forty patients with reticuloendotheliosis seen at the Johns Hopkins Hospital are presented. These are classified as cases of Letterer-Siwe disease, Schuller-Christian disease and eosinophilic granuloma on the basis of the number and extent of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a526087a7f257526f5a26e4298c7cd3
https://doi.org/10.1016/0002-9343(57)90115-8
https://doi.org/10.1016/0002-9343(57)90115-8
Publikováno v:
The Journal of Pediatrics. 41:722-739
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db9e50e65d94bf998807cb53d3e2da6d
https://doi.org/10.1016/s0022-3476(52)80293-8
https://doi.org/10.1016/s0022-3476(52)80293-8
Publikováno v:
Blood. 36:576-585
Three unrelated, Caucasian patients with a disorder resembling infantile genetic agranulocytosis have been studied. There was no history of consanguinity. Parents and siblings were normal. Onset occurred before 3 weeks of age and persisted throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c018ba2382750d5d3fef3efa1cdf1f2b
https://doi.org/10.1182/blood.v36.5.576.576
https://doi.org/10.1182/blood.v36.5.576.576
Autor:
Harriet G. Guild, James R. Cantrell
Publikováno v:
American journal of surgery. 108
1. 1. Congenital stenosis of the trachea is a relatively uncommon anomaly yet one which should be recognized since in many instances the lesion is susceptible to correction. 2. 2. The presence of stridor, dyspnea and cyanosis in a newborn infant or s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd4c74ead7210500a1adc84e448b75b
https://pubmed.ncbi.nlm.nih.gov/14195226
https://pubmed.ncbi.nlm.nih.gov/14195226
Publikováno v:
American journal of ophthalmology. 35(9)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63414dbb756b030d21fb63b7625a65a0
https://pubmed.ncbi.nlm.nih.gov/12976494
https://pubmed.ncbi.nlm.nih.gov/12976494