Zobrazeno 1 - 10
of 16
pro vyhledávání: '"C. M. Meyers"'
Autor:
D. McCorkle, C. M. Meyers, Wayne S. Stanley, Richard I. Kelley, D. P. Bick, H. J. Stern, G. D. Berkovitz, P. Staszak
Publikováno v:
Prenatal Diagnosis. 19:68-71
A cytogenetically normal male fetus was subsequently found to have female external genitalia, a cardiac malformation and mid-trimester intra-uterine growth retardation by ultrasound examination. The maternal serum oestriol level was low. The combinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757a7b2adef870d7f57664e87d039ace
https://doi.org/10.1002/(sici)1097-0223(199901)19:1<68::aid-pd461>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199901)19:1<68::aid-pd461>3.0.co
Autor:
M C, Provost, C M, Meyers
Publikováno v:
Contributions to nephrology. (133)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a22755c1a39300333b31eecb6532aad7
https://pubmed.ncbi.nlm.nih.gov/11477743
https://pubmed.ncbi.nlm.nih.gov/11477743
Autor:
Steven J. Birkos, C. M. Meyers
Publikováno v:
Immunogenetics. 50(1-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2312fcaff7a56552d980c0952bc5dff0
https://pubmed.ncbi.nlm.nih.gov/10541810
https://pubmed.ncbi.nlm.nih.gov/10541810
Publikováno v:
American journal of medical genetics. 84(1)
The omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex is a consistent and recognizable pattern of midline abdominal and pelvic defects. It is rare, affecting 1 in 200,000 to 400,000 pregnancies and is even rarer in twin gestations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63fad73addbd57e9ae3e00300991fa1f
https://pubmed.ncbi.nlm.nih.gov/10213043
https://pubmed.ncbi.nlm.nih.gov/10213043
Autor:
D P, Bick, D, McCorkle, W S, Stanley, H J, Stern, P, Staszak, G D, Berkovitz, C M, Meyers, R I, Kelley
Publikováno v:
Prenatal diagnosis. 19(1)
A cytogenetically normal male fetus was subsequently found to have female external genitalia, a cardiac malformation and mid-trimester intra-uterine growth retardation by ultrasound examination. The maternal serum oestriol level was low. The combinat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff14263301be52ab5eaea7a8a4501adb
https://pubmed.ncbi.nlm.nih.gov/10073912
https://pubmed.ncbi.nlm.nih.gov/10073912
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 161(10)
To investigate mechanisms of cell-mediated events in chronic glomerulonephritis, T cell clones were isolated from kidneys of animals with murine chronic graft-vs-host disease. This systemic disorder is induced in normal (C57BL/6 x DBA/2)F1 recipients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::268bf123144dcd5c016b33358c5f2e9c
https://pubmed.ncbi.nlm.nih.gov/9820505
https://pubmed.ncbi.nlm.nih.gov/9820505
Autor:
A E, Tretter, R C, Saunders, C M, Meyers, J S, Dungan, K, Grumbach, C C, Sun, A B, Campbell, E A, Wulfsberg
Publikováno v:
American journal of medical genetics. 75(5)
Lethal skeletal dysplasias (LSD) are a heterogeneous group of rare but important genetic disorders characterized by abnormal growth and development of bone and cartilage. We describe the diagnosis and outcome of 29 cases of lethal skeletal dysplasias
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5756735e75a01105a96a548da37193c
https://pubmed.ncbi.nlm.nih.gov/9489797
https://pubmed.ncbi.nlm.nih.gov/9489797
Publikováno v:
Maryland medical journal (Baltimore, Md. : 1985). 46(2)
Maternal serum screening for the detection of fetal Down syndrome has become widespread. Prenatal detection of fetal Down syndrome has important implications not only for management of the current pregnancy, but also for recurrence risk counseling fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::39ee1a88abba61eb77b8e48183384b09
https://pubmed.ncbi.nlm.nih.gov/9029908
https://pubmed.ncbi.nlm.nih.gov/9029908
Publikováno v:
American journal of medical genetics. 63(4)
Gonadal (ovarian) dysgenesis with normal chromosomes (46,XX) clearly is a heterogeneous condition. In some forms, the defect is restricted to the gonads, whereas other affected females show neurosensory hearing loss (Perrault syndrome). In another fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f91983a0c6b5091526e70cb19dfc738a
https://pubmed.ncbi.nlm.nih.gov/8826428
https://pubmed.ncbi.nlm.nih.gov/8826428
Autor:
C. M. Meyers, C. J. Kelly
Publikováno v:
Immunology of Renal Disease ISBN: 9789401057387
Primary tubulointerstitial nephritis causes a significant proportion of both acute and chronic renal disease1. Advances in our knowledge of clinicopathological correlates, moreover, have also established a prognostic importance for the tubulointersti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef18c1905b6ec2341cde8a6c2af30f6f
https://doi.org/10.1007/978-94-011-3902-1_13
https://doi.org/10.1007/978-94-011-3902-1_13
