Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Ryan E. Longman"'
Publikováno v:
Frontiers in Immunology, Vol 10 (2020)
Understanding what happens at the time of embryo implantation has been the subject of significant research. Investigators from many differing fields including maternal fetal medicine, microbiology, genetics, reproductive endocrinology and immunology
Externí odkaz:
https://doaj.org/article/6eb3ac72f76c4a02a88941cd5a22ed4c
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca1652826e30d0fee0a4ed9d19fbe1c5
https://doi.org/10.1055/a-2011-6037
https://doi.org/10.1055/a-2011-6037
Autor:
Desiree G. Fiorentino, Ryan E. Longman
Publikováno v:
First-Trimester Ultrasound ISBN: 9783031241321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d18d254c4b210d18d1e484679bfe9f37
https://doi.org/10.1007/978-3-031-24133-8_21
https://doi.org/10.1007/978-3-031-24133-8_21
Publikováno v:
First-Trimester Ultrasound ISBN: 9783031241321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d6ef193606e7648714fd17fe8298f87
https://doi.org/10.1007/978-3-031-24133-8_3
https://doi.org/10.1007/978-3-031-24133-8_3
Publikováno v:
First-Trimester Ultrasound ISBN: 9783031241321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f95ae0b43d0adf99c0c681496b329083
https://doi.org/10.1007/978-3-031-24133-8_9
https://doi.org/10.1007/978-3-031-24133-8_9
Autor:
Jacques S. Abramowicz, Ryan E. Longman
This second edition offers a unique and focused study of the use of ultrasound during the first trimester, a critical time in a fetus'development. It includes basic examination guidelines as well as cutting-edge ultrasound modalities, including Doppl
Autor:
Ryan E. Longman, Carol Holland, Catherine Terhaar, Nicole Teed, Lindsay Dohany, Rachel Allen, Christina Settler
Publikováno v:
Prenatal Diagnosis
Objectives Expanded carrier testing is acknowledged as an acceptable strategy for carrier testing by the American College of Obstetrics and Gynecology. Limited studies have investigated positivity rates of expanded carrier panels. We describe our exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77be3f76ddea71f8f27ef1d32acf21f
https://doi.org/10.1002/pd.5272
https://doi.org/10.1002/pd.5272
Autor:
Christina Settler, Ryan E. Longman, Jeana DaRe, Tobias Mann, Carol Holland, Kailey M. Owens, Lindsay Dohany
Publikováno v:
American Journal of Medical Genetics Part A. 176:1304-1308
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and is caused by an expansion of cytosine-guanine-guanine (CGG) repeats in the FMR1 gene. Female premutation allele carriers (55-200 CGG repeats) are at risk to ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78ddc42fb206c31b56f77e4abf31a01
https://doi.org/10.1002/ajmg.a.38692
https://doi.org/10.1002/ajmg.a.38692
Autor:
Sonya S. Abdel-Razeq, Yalda Afshar, Marta Arigita, Abigail A. Armstrong, Mert Ozan Bahtiyar, Ahmet Baschat, Marc U. Baumann, Mar Bennasar, Richard L. Berkowitz, Amar Bhide, Harm-Gerd K. Blaas, April T. Bleich, Rachael J. Bradshaw, Thorsten Braun, Fallon R. Brewer, Angela Burgess, Alison G. Cahill, Katherine H. Campbell, Frederic Chantraine, Tamara T. Chao, Debnath Chatterjee, Jaclyn M. Coletta, Elena Contro, Joshua A. Copel, Fatima Crispi, Timothy M. Crombleholme, Sarah N. Cross, Mónica Cruz-Lemini, Rogelio Cruz-Martínez, Andrea Dall'Asta, Mary E. D'Alton, Francesco D'Antonio, Jodi S. Dashe, Luc De Catte, Francesca De Musso, Valentina De Robertis, Jan Deprest, Roland Devlieger, Anke Diemert, Lindsey Drehfal, Elisenda Eixarch, Alexander Engels, Jakob Evers, Tiziana Fanelli, Helen Feltovich, Susana Fernández, Francesc Figueras, Perry Friedman, Tiziana Frusca, Karin M. Fuchs, Julie A. Gainer, France Galerneau, Stephanie L. Gaw, Kobina Ghartey, Tullio Ghi, Katherine R. Goetzinger, Olga Gómez, Eduard Gratacós, Carole Gravino, Maureen S. Hamel, Christina S. Han, Lorie M. Harper, Wolfgang Henrich, Jennifer S. Hernandez, Mauricio Herrera, Cara C. Heuser, June Y. Hou, Michael House, Lisa W. Howley, Rebecca S. Hulinsky, Jon A. Hyett, G. Marc Jackson, Joses A. Jain, Anthony Johnson, Clark T. Johnson, Franz Kainer, Karim D. Kalache, Katherine S. Kohari, Deborah Krakow, Wesley Lee, Tally Lerman-Sagie, Liesbeth Lewi, Ling Li, Heather S. Lipkind, Ryan E. Longman, Adetola F. Louis-Jacques, Lindsay Maggio, Urania Magriples, Gustavo Malinger, Stephanie Martin, Josep M. Martinez, Ahmed I. Marwan, Audrey Merriam, Silke A.M. Michaelis, Jena Miller, Russell S. Miller, Anne-Elodie Millischer, Ana Monteagudo, Leslie Moroz, Claudia Mosquera, Unzila A. Nayeri, Sarah Običan, Anthony O. Odibo, Dotun Ogunyemi, Aris T. Papageorghiou, Felicity J. Park, Christian M. Pettker, Gianluigi Pilu, Lawrence D. Platt, Bienvenido Puerto, Melissa Quinn, Luigi Raio, Georgios Rembouskos, Ivan M. Rosado-Mendez, Andrea Rossi, Francesca Maria Russo, Laura Salazar, Laurent J. Salomon, Amber Samuel, Magdalena Sanz-Cortés, Anna Katerina Sfakianaki, Jeanne S. Sheffield, Sara Shelley, Michelle Silasi, Robert Silver, Lynn L. Simpson, Rachel G. Sinkey, Saul Snowise, Pascale Sonigo, Hindi E. Stohl, Jens H. Stupin, Ilan E. Timor-Tritsch, Ants Toi, Gloria Too, Boris Tutschek, Methodius G. Tuuli, Ignatia B. Van den Veyver, Tim Van Mieghem, Joy Vink, Paolo Volpe, Carmela Votino, Jennifer M. Walsh, Erika F. Werner, Lisa C. Zuckerwise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af51d15ebfe17d9ddf4df268606b2c06
https://doi.org/10.1016/b978-0-323-44548-1.00177-7
https://doi.org/10.1016/b978-0-323-44548-1.00177-7
Autor:
Ryan E. Longman
CHARGE syndrome is an autosomal dominant disorder characterized by multiple congenital malformations along with developmental and cognitive impairments. The incidence of CHARGE syndrome is 1 : 8500 to 1 : 10,000. The only known genetic etiology for C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16133a116708098c945426f46b6879fb
https://doi.org/10.1016/b978-0-323-44548-1.00126-1
https://doi.org/10.1016/b978-0-323-44548-1.00126-1