Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Gerald S. Spear"'
Publikováno v:
Obstetrics & Gynecology. 92:702-705
Background: Spontaneous neonatal thrombosis due to heritable gene defects has been reported in the past. A recently discovered defect, the factor V Leiden mutation, is the most frequent inherited risk factor for venous thrombosis. Case: Factor V Leid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e0a121a538891222a64a257c6c4704b
https://doi.org/10.1016/s0029-7844(98)00065-9
https://doi.org/10.1016/s0029-7844(98)00065-9
Publikováno v:
Obstetrics & Gynecology. 92:702-705
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a1a8506d27b483460a39e868a35f878
https://doi.org/10.1097/00006250-199810001-00028
https://doi.org/10.1097/00006250-199810001-00028
Autor:
Kim M. Swenson, David K. Imagawa, Bibo Ke, Jay S. Markowitz, Tao Wang, Gerald S. Spear, Ronald W. Busuttil, Philip Seu, John A. Goss, Melinda A. Maggard
Publikováno v:
Transplantation. :155-160
Background. Fas ligand (FasL) induces apoptosis of cells bearing its receptor Fas, and has been shown to be important in T-cell development and regulation and in immune privilege. We hypothesized that FasL expression by renal allografts might provide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cf76d87679bb785ece548edd9eae7a1
https://doi.org/10.1097/00007890-199801270-00002
https://doi.org/10.1097/00007890-199801270-00002
Autor:
Gerald S. Spear
Publikováno v:
The Journal of heredity. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1365bd015435be3382cf6299b557def
https://pubmed.ncbi.nlm.nih.gov/20995084
https://pubmed.ncbi.nlm.nih.gov/20995084
Publikováno v:
Fetal and pediatric pathology. 26(3)
The findings in a stillborn female fetus of 31 weeks' gestation with congenital Gaucher disease, nonimmune hydrops/erythroblastosis, infantile arterial calcification, and neonatal hepatitis/fibrosis are presented, the first report of this complete co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7074b791aa0a2215438fa0c4167c2a2
https://pubmed.ncbi.nlm.nih.gov/17886025
https://pubmed.ncbi.nlm.nih.gov/17886025
Autor:
Gerald S. Spear
Publikováno v:
American journal of medical genetics. Part A. 140(21)
The findings in a newborn male with agenesis of parietal bones, gracile long bones, and hypoplasia of the spleen are presented. Although parietal agenesis is unique, the findings are compatible with 18 previously reported cases characterized by crani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d486c6b29a1cf0a12639b48999d8a2e
https://pubmed.ncbi.nlm.nih.gov/17036309
https://pubmed.ncbi.nlm.nih.gov/17036309
Autor:
David L. Rimoin, Gerald S. Spear, Alison M. Elliott, Fiona M. Field, Thora S. Steffensen, Ralph S. Lachman, William R. Wilcox, Barbara D. Friedman
Publikováno v:
American journal of medical genetics. Part A. 140(14)
Osteocraniostenosis is a severe skeletal dysplasia characterized by a hypomineralized skull that has been previously described as kleeblattschadel (cloverleaf skull) and overtubulated long bones. Dysmorphic facial features include a short nose, short
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75af24cecb5b081c8bc2bb65629cdd4c
https://pubmed.ncbi.nlm.nih.gov/16770805
https://pubmed.ncbi.nlm.nih.gov/16770805
Publikováno v:
American Journal of Roentgenology. 159:628-630
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf38bbff3e7f2a3db1e5ee1b4b6446c8
https://doi.org/10.2214/ajr.159.3.1503040
https://doi.org/10.2214/ajr.159.3.1503040
Publikováno v:
Pediatric Nephrology. 6:312-312
An 18-week fetus was born following termination of pregnancy by prostaglandin induction. Pregnancy was terminated because of elevated maternal serum alpha-fetoprotein and ultrasonographic evidence of severe oligohydramnios, intrauterine growth retard
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4c38f221565f37c6c91ec81d0834478
https://doi.org/10.1007/bf00878386
https://doi.org/10.1007/bf00878386