Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Logan B. Karns"'
Autor:
Maria Antero, J. Kim Penberthy, Semara A. Thomas, Karen Ventura, Lisa M. Pastore, Logan B. Karns
Publikováno v:
Journal of Genetic Counseling. 23:968-975
Diminished ovarian reserve (DOR) and premature ovarian failure are associated with elevated FMR1 CGG repeat alleles. We assessed pretest attitudes about potentially carrying the FMR1 premutation (FXP) (>55 CGG repeats) among reproductive age women co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a591845370377dd9882d70a7a3daa01d
https://doi.org/10.1007/s10897-014-9717-4
https://doi.org/10.1007/s10897-014-9717-4
Autor:
Richard H. Steeves, Myra L. Clark, Logan B. Karns, Lisa M. Pastore, Karen Ventura, Nancy Callanan
Publikováno v:
Journal of Genetic Counseling. 23:97-107
About 10 % of infertile/subfertile women are diagnosed with diminished ovarian reserve (DOR), of which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5cbee620c6aac6bb3e3482306e57529
https://doi.org/10.1007/s10897-013-9616-0
https://doi.org/10.1007/s10897-013-9616-0
Publikováno v:
Prenatal Diagnosis. 28:1251-1255
Objective We theorized that a significant number of women would choose integrated screening (IS) over first trimester screening (FTS) and that demographic characteristics and baseline anxiety levels might predict which patients would choose each test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90a278c98cdaa04bf4259c018c065530
https://doi.org/10.1002/pd.2158
https://doi.org/10.1002/pd.2158
Publikováno v:
Journal of Genetic Counseling. 17:84-91
Female fragile X premutation carriers are at approximately 10-fold increased risk of premature ovarian failure (follicle stimulating hormone40 mIU/mL, amenorrhea, age40). A milder degree of premature ovarian aging (diminished ovarian reserve, where f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a3b1f4c624e650e87b95aa4b82946c4
https://doi.org/10.1007/s10897-007-9129-9
https://doi.org/10.1007/s10897-007-9129-9
Autor:
K. H. Mooney, S. Schmerler, Logan B. Karns, Nancy Callanan, Scott M. Weissman, R. Ruzicka, Robin L. Bennett, E. Gordon
Publikováno v:
Journal of Genetic Counseling. 15:313-323
The Code of Ethics (COE) of the National Society of Genetic Counselors (NSGC) was adopted in 1992. In 2004, the NSGC leadership appointed the Code of Ethics Work Group (COEWG) to consider revisions to the NSGC COE based on advice from the NSGC legal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b001b14337cbcd0672c972b30103d777
https://doi.org/10.1007/s10897-006-9043-6
https://doi.org/10.1007/s10897-006-9043-6
Autor:
Lawrence M. Silverman, Christopher D. Williams, Teresa R. Camp, Lisa M. Pastore, Logan B. Karns, JoAnn V. Pinkerton
Publikováno v:
American Journal of Obstetrics and Gynecology. 194:738-743
Objective The purpose of this study was to assess patient perception of fragile X premutation genetic testing (FRAX). Study design This was a cross-sectional survey of women with elevated follicle stimulating hormone levels with (premature ovarian fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e782f3a1b75cfdbb1896c793c442c9
https://doi.org/10.1016/j.ajog.2005.10.218
https://doi.org/10.1016/j.ajog.2005.10.218
Publikováno v:
American Journal of Obstetrics and Gynecology. 187:296-301
This review of end-of-life decisions centers on the role of the obstetrician/gynecologist in assisting women patients to develop advanced directives that are targeted to unique risks of the pregnant woman; these risks are related to trauma, cancer, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c79ef7178bfd7fb005e335afc44b7208
https://doi.org/10.1067/mob.2002.125701
https://doi.org/10.1067/mob.2002.125701
Publikováno v:
Journal of genetic counseling. 21(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c87747bc0752b0c91b06f81387a87aff
https://pubmed.ncbi.nlm.nih.gov/22639327
https://pubmed.ncbi.nlm.nih.gov/22639327
Publikováno v:
American Journal of Medical Genetics. 102:136-138
Bloom syndrome is a rare autosomal recessive disorder notable for increased chromosome fragility and an increased rate of somatic mutation. The clinical manifestations include small stature, a characteristic dermatologic lesion, and an excess inciden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb44dcf66cb8724009a69e905236355c
https://doi.org/10.1002/ajmg.1437
https://doi.org/10.1002/ajmg.1437
Publikováno v:
Prenatal diagnosis. 28(13)
We theorized that a significant number of women would choose integrated screening (IS) over first trimester screening (FTS) and that demographic characteristics and baseline anxiety levels might predict which patients would choose each test. We also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86a0a1e56598bb7a601aa110063dd1e2
https://pubmed.ncbi.nlm.nih.gov/19097030
https://pubmed.ncbi.nlm.nih.gov/19097030