John Gardner and the morality of choice

Autor: James C. Schaap

Publikováno v: Koers : Bulletin for Christian Scholarship, Vol 61, Iss 1 (1996)

Although interest in literary theory has prompted much discussion concerning the relationship between literature and religious worldview, that discussion has taken place primarily among theorists and not practitioners. Christian writers have few cont

Externí odkaz: https://doaj.org/article/8a9ca7433b7c4cceaf8da1f41b5aa81e

Differential effects of nonselective versus selective β-blockers on cardiac sympathetic activity and hemostasis in patients with heart failure

Autor: Rienk Nieuwland, Wouter E.M. Kok, Hein J. Verberne, Ad Bakx, Pieter Willem Kamphuisen, Olav R. de Peuter, G. Aernout Somsen, Marianna C. Schaap, Bas van den Bogaard, Joost C. M. Meijers

Publikováno v: Journal of Nuclear Medicine, 54(10), 1733-1739. SOC NUCLEAR MEDICINE INC
Journal of nuclear medicine, 54(10), 1733-1739. Society of Nuclear Medicine Inc.

Carvedilol, a nonselective β-blocker, may be more effective than the selective β-blocker metoprolol in reducing the risk of thromboembolic events in heart failure. The aim of this study was, first, to assess whether there is a differential response

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de2afe57d9d7f20854fbbba7e3556f12
https://research.rug.nl/en/publications/d5cd84d6-d733-49ee-b19e-b0d63a3b87e8

Two novel and one recurrent missense mutation in the factor XIII A gene in two Dutch patients with factor XIII deficiency

Autor: E B, Gómez García, S R, Poort, J, Stibbe, A, Sturk, M C, Schaap, M, Kappers, R M, Bertina

Publikováno v: British journal of haematology. 112(2)

Congenital factor XIII (FXIII) deficiency is a rare autosomal recessive disorder, usually attributed to a defect in the FXIII A subunit, whose genetic basis has been studied in a number of cases. We describe here the genetic variations found in two u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c875d744a96d806981c5bb474f006d77
https://pubmed.ncbi.nlm.nih.gov/11167856

Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

Autor: H C, Janssen, C, Schaap, N, Vandevijver, P, Moerman, C E, de Die-Smulders, J P, Fryns

Publikováno v: Journal of medical genetics. 36(6)

We report two sibs of Turkish descent with multiple congenital anomalies including severe microcephaly, hygroma colli, cystic renal dysplasia, and bilateral cutaneous syndactyly of toes IV-V. In addition, the second sib presented with bilateral fusio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3f244a59e5b81cfbff5f923f629c442b
https://pubmed.ncbi.nlm.nih.gov/10874639

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer

Autor: P M Khan, Lucio Bertario, Adri Mulder, C Schaap, Ketil Heimdal, Han G. Brunner, Pål Møller, Riccardo Fodde, C. Tops, P. Goetz, Gerrit Griffioen, J.G. Post, Juul T. Wijnen, Dick Lindhout, Martijn H. Breuning, Fokko N. Nagengast, Jaran Apold, van Leeuwen-Cornelisse, Rolf H. Sijmons, Egbert Bakker, Marie Luise Bisgaard, Ahjt Brocker-Vriends, A Meijers-Heijboer, B. G. Taal, Aeilko H. Zwinderman, Fred H. Menko, Jan H. Kleibeuker, H. F. A. Vasen, H. van der Klift

Publikováno v: ResearcherID
New England journal of medicine, 339(8), 511-518. Massachussetts Medical Society
New England Journal of Medicine, 339(8), 511-518. MASSACHUSETTS MEDICAL SOC

Background Germ-line mutations in DNA mismatch-repair genes (MSH2, MLH1, PIMS1, PMS2, and MSH6) cause susceptibility to hereditary nonpolyposis colorectal cancer. We assessed the prevalence of MSH2 and MLH1 mutations in families suspected of having h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bca113090b3a1a1d7c066d495ccb1c0
https://pubmed.ncbi.nlm.nih.gov/9709044