Zobrazeno 1 - 10
of 59
pro vyhledávání: '"D. Axworthy"'
Publikováno v:
Prenatal Diagnosis. 17:853-860
A comparative study of women who underwent prenatal cystic fibrosis (CF) carrier screening by either the 'two-step method' or the 'couple method' was carried out 2-4 years after testing. Recall of the screening test and test result, understanding of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4257a15439c56f1f513da86c72fbaba5
https://doi.org/10.1002/(sici)1097-0223(199709)17:9<853::aid-pd151>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199709)17:9<853::aid-pd151>3.0.co
Publikováno v:
The Lancet. 347:1443-1446
Summary Background The objective of this study was to show the long-term psychological effects of population-based screening for cystic fibrosis. Methods The sample comprised all carriers (n=435) and, for each carrier, two matched screen-negative ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdad9e36dde3335c47be8ddcf50434c2
https://doi.org/10.1016/s0140-6736(96)91683-9
https://doi.org/10.1016/s0140-6736(96)91683-9
Publikováno v:
Cancer research. 60(23)
Single-chain Fv antibody fragments from the CD20-specific murine monoclonal antibody B9E9 were genetically engineered as streptavidin fusions [single-chain Fv-streptavidin (scFvSA) fusion protein] for use in pretargeted radioimmunotherapy. The scFvSA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd67bd0fe12966004a292f48a61044f5
https://pubmed.ncbi.nlm.nih.gov/11118050
https://pubmed.ncbi.nlm.nih.gov/11118050
Autor:
S J, Knox, M L, Goris, M, Tempero, P L, Weiden, L, Gentner, H, Breitz, G P, Adams, D, Axworthy, S, Gaffigan, K, Bryan, D R, Fisher, D, Colcher, I D, Horak, L M, Weiner
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 6(2)
A Phase II study of yttrium-90-tetra-azacyclododecanetetra-acetic acid-biotin (90Y-DOTA-biotin) pretargeted by NR-LU-10 antibody/streptavidin (SA) was performed. The primary objectives of the study were to evaluate the efficacy and safety of this the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::962d544ea1d060a1e6383268f4555b29
https://pubmed.ncbi.nlm.nih.gov/10690517
https://pubmed.ncbi.nlm.nih.gov/10690517
Publikováno v:
Prenatal diagnosis. 17(9)
A comparative study of women who underwent prenatal cystic fibrosis (CF) carrier screening by either the 'two-step method' or the 'couple method' was carried out 2-4 years after testing. Recall of the screening test and test result, understanding of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd040ee528eb6e3b53bf18a5f2771c2f
https://pubmed.ncbi.nlm.nih.gov/9316130
https://pubmed.ncbi.nlm.nih.gov/9316130
Publikováno v:
Lancet (London, England). 347(9013)
The objective of this study was to show the long-term psychological effects of population-based screening for cystic fibrosis.The sample comprised all carriers (n = 435) and, for each carrier, two matched screen-negative individuals (n = 870) detecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33dd2d71cd8e5284fb875d98668733dd
https://pubmed.ncbi.nlm.nih.gov/8676620
https://pubmed.ncbi.nlm.nih.gov/8676620
Publikováno v:
BMJ. 308:658-659
EDITOR, - The Human Fertilisation and Embryology Authority has recently published a public consultation document, Donated Ovarian Tissue in Embryo Research and Assisted Conception.1,2 This document discusses the “issues surrounding the use in resea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52e33b67470979ce28a5e7415e720fd9
https://doi.org/10.1136/bmj.308.6929.658b
https://doi.org/10.1136/bmj.308.6929.658b
Publikováno v:
Journal of Medical Genetics. 21:45-51
Thirty-six infants were identified by cytogenetic screening at birth as having balanced rearrangements of their autosomes, and 30 of them took part in a longitudinal study of their development, together with four of their affected sibs. With the exce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7a6caa67361732a5f7118cfcbd893e
https://doi.org/10.1136/jmg.21.1.45
https://doi.org/10.1136/jmg.21.1.45
Publikováno v:
Human Genetics. 55:31-38
Trisomy 8, in mosaic or non-mosaic form is an extremely rare chromosomal condition in man. Liveborn subjects usually present with mental retardation, bone and joint anomalies and a variety of other physical anomalies. The mental retardation associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c00ae7a51da69e8f00fbc39aeb0f24d
https://doi.org/10.1007/bf00329123
https://doi.org/10.1007/bf00329123
Publikováno v:
Birth defects original article series. 15(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d3acd66d68c2d6db3744b3bb792ea7a
https://pubmed.ncbi.nlm.nih.gov/444643
https://pubmed.ncbi.nlm.nih.gov/444643