Zobrazeno 1 - 10
of 253
pro vyhledávání: '"Enid Gilbert, Barness"'
Publikováno v:
Translational Science of Rare Diseases. 1:3-22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5b9f52b1f1ec9e42cf749f1941bc3d0
https://doi.org/10.3233/trd-160001
https://doi.org/10.3233/trd-160001
Publikováno v:
American Journal of Medical Genetics Part A. 167:478-503
Noted for centuries in humans, a relatively hairless mammal [e.g., Hallero, 1766; Hohl, 1828 in Klunker, 2003], the so-called amniotic deformities, adhesions, mutilations (ADAM) sequence remains causally and pathogenetically incognito. In 1930 Street
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f235d2e58f9ea226178c90c28a39268
https://doi.org/10.1002/ajmg.a.36937
https://doi.org/10.1002/ajmg.a.36937
Autor:
Enid Gilbert-Barness, M. Daria Haust
Publikováno v:
Pediatric and Developmental Pathology. 17:165-168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ff5ae3bb8f5a3c697c876fb2851d904
https://doi.org/10.2350/14-02-1442-pb.1
https://doi.org/10.2350/14-02-1442-pb.1
Publikováno v:
Fetal and Pediatric Pathology. 31:39-42
We report on a case of a prenatally diagnosed non-immune hydrops fetalis and cystic hygroma associated with the balanced translocation t(5;9)(q11.2;p22), an association that to our knowledge has not been reported previously. Both parents had normal k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceddf1e95ede493451532f2aaff9ff4c
https://doi.org/10.3109/15513815.2011.641891
https://doi.org/10.3109/15513815.2011.641891
Autor:
Thordur Thorkelsson, Thora S. Steffensen, Enid Gilbert-Barness, Jens A. Gudmundsson, Cameron K. Tebbi
Publikováno v:
Fetal and Pediatric Pathology. 30:77-87
A case of a premature infant with lactic acidosis and hepatic iron accumulation, born to a mother with multiple fetal demises, is presented and discussed by both clinician and pathologist, in this traditional clinico-pathologic conference. The discus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0100be29b3dae61c2fdc86a41c32f953
https://doi.org/10.3109/15513815.2011.546142
https://doi.org/10.3109/15513815.2011.546142
Publikováno v:
Fetal and Pediatric Pathology. 28:216-231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e35a2348c8be6915f6dc697f5dd43ac
https://doi.org/10.1080/15513810903073682
https://doi.org/10.1080/15513810903073682
Autor:
William N. Spellacy, John C.M. Tsibris, Enid Gilbert-Barness, Joan M. McCarthy, Katheryne Downes
Publikováno v:
Fetal and Pediatric Pathology. 28:239-246
Objective: To determine the correlation of histological chorioamnionitis (CA) with and without clinical CA with umbilical cord blood gases, erythropoietin (EPO), and interleukin-6 (IL-6) levels. Methods: Umbilical artery blood gas analysis (pH, pO2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9712e25d26f0f97d11efea4417c58186
https://doi.org/10.1080/15513810903139699
https://doi.org/10.1080/15513810903139699
Publikováno v:
Fetal and Pediatric Pathology. 28:47-54
Insulin-like growth factor 1 and its receptor (IGF-1/IGF-2) may play important roles in the development of human fetal tissue, and its ligands IGF-1 and IGF-2 have been found in fetuses older than 3 months. Our objective was to study the immunohistoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f3350d3c32616ed435576e1d9dc20e4
https://doi.org/10.1080/15513810802679498
https://doi.org/10.1080/15513810802679498
Publikováno v:
Fetal and Pediatric Pathology. 28:24-38
The Aicardi syndrome is characterized by infantile spasms, corpus callosum agenesis, and chorioretinal lacunae and almost exclusively affects females (very rarely, 47, XXY males). The crucial genetic mishap likely occurs in the postzygotic stage, but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c798cefb81fcf832fcd2522087ba78a
https://doi.org/10.1080/15513810802545319
https://doi.org/10.1080/15513810802545319
Autor:
Frederick Nora, E. Verena Jorgensen, Enid Gilbert-Barness, Lanita C. Witt, Thora S. Steffensen
Publikováno v:
Fetal and Pediatric Pathology. 27:245-258
A case of bilateral gonadoblastoma in 46,XY gonadal dysgenesis is presented and discussed by both clinician and pathologist, in this traditional clinico-pathologic conference. The discussion includes the differential diagnoses of primary amenorrhoea.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::540f801d1bdecf44b9a604a9efa31c5d
https://doi.org/10.1080/15513810802447920
https://doi.org/10.1080/15513810802447920