Zobrazeno 1 - 8
of 8
pro vyhledávání: '"SuEllen Toth-Fejel"'
Autor:
Kristine Calhoun, Nicole Dumas, SuEllen Toth-Fejel, Bruce Ham, Rodney F. Pommier, Patrick Muller, Kevin M. Esvelt
Publikováno v:
Annals of Surgical Oncology. 11:560-567
Detection of systemic breast cancer recurrence is limited by lack of universally expressed tumor cell markers. We hypothesized that a test that detects genetic alterations specific to breast cancer cells of an individual patient would provide a super
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac3fccb06d5c0edfa7be06fc38a0bf4
https://doi.org/10.1245/aso.2004.03.049
https://doi.org/10.1245/aso.2004.03.049
Autor:
David K. Grandy, Kristine Gunter, Shoko Hagen, Zhu Wei Zhu, SuEllen Toth-Fejel, Qun-Yong Zhou, Susan Olson
Publikováno v:
Analgesia. 1:446-449
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d6f3f46543e51b3edbdc3ae2ade505b
https://doi.org/10.3727/107156995819563456
https://doi.org/10.3727/107156995819563456
Publikováno v:
Endocrinology. 143(6)
Ovarian cancer is the most lethal gynecological cancer, and approximately 90% of ovarian cancers derive from the ovarian surface epithelium (OSE), yet the biology of the OSE is poorly understood. Factors associated with increased risk of nonhereditar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d04eb24becc392bc808670b66e24a57
https://pubmed.ncbi.nlm.nih.gov/12021183
https://pubmed.ncbi.nlm.nih.gov/12021183
Autor:
SuEllen Toth-Fejel, R. Ellen Magenis
Publikováno v:
Prader-Willi Syndrome ISBN: 9783642842856
The Prader-Willi Syndrome (PWS) was recognized as a clinical entity (Prader et al, 1956) over 30 years prior to the finding of the deletion that is now observed in the majority of cases (Ledbetter et al, 1981). The clinical features, which include hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dcb1e12b4ae432a9cd7c4bdc423fc6e
https://doi.org/10.1007/978-3-642-84283-2_8
https://doi.org/10.1007/978-3-642-84283-2_8
Autor:
SuEllen Toth-Fejel, Kristine Calhoun, Rodney F. Pommier, Judith Lacy, Katherine T. Morris, Julie Cheek
Publikováno v:
Archives of Surgery. 137:1015
Hypothesis Patients who receive hormone replacement therapy (HRT) and subsequently develop breast cancer are more likely to be diagnosed by palpation than mammography and have a higher stage of cancer at initial diagnosis. Design Retrospective case s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf06dd86bc32d06df820916f6c01546
https://doi.org/10.1001/archsurg.137.9.1015
https://doi.org/10.1001/archsurg.137.9.1015
Autor:
Gregory L. Beagle, Katherine T. Morris, John T. Vetto, Waldemar A. Schmidt, Rodney F. Pommier, Josh Schmidt, SuEllen Toth-Fejel, Priscilla W. Alexander, Arden M. Morris
Publikováno v:
Archives of Surgery. 136:1008
Hypothesis The triple test score (TTS) is useful and accurate for evaluating palpable breast masses. Design Diagnostic test study. Setting University hospital multidisciplinary breast clinic. Patients Four hundred seventy-nine women with 484 palpable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c3e6c1ffc8cb5f50e3ef388f7d0f577
https://doi.org/10.1001/archsurg.136.9.1008
https://doi.org/10.1001/archsurg.136.9.1008
Autor:
Neil R. M. Buist, R.E. Magenis, R. Rettenmeier, Gerd Scherer, E.-M. Westphal, E. Natt, SuEllen Toth-Fejel
Publikováno v:
Human genetics. 77(4)
Tyrosinemia II is an autosomal-recessively inherited condition caused by deficiency in the liver-specific enzyme tyrosine aminotransferase (TAT; EC 2.6.1.5). We have restudied a patient with typical symptoms of tyrosinemia II who in addition suffers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::767ded20b9c7703ccb634f4233508e5a
https://pubmed.ncbi.nlm.nih.gov/2891604
https://pubmed.ncbi.nlm.nih.gov/2891604
Autor:
Charles D. Boyd, Karl Tryggvason, Ellen Magenis, Susan B. Deak, Angela M. Christiano, SuEllen Toth-Fejel, James W. Mackenzie, Karen Weliky, Linda J. Sandell
Publikováno v:
Human genetics. 74(2)
Using dual-laser sorted chromosomes and spot-blot analysis, we have previously assigned genomic DNA sequences coding for human alpha 1 (IV) procollagen to chromosome 13 (Pihlajaniemi et al. 1985). By in situ hybridization to normal chromosomes and ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a72b9a19f72d265a3cafdde0f8762a63
https://pubmed.ncbi.nlm.nih.gov/3770740
https://pubmed.ncbi.nlm.nih.gov/3770740