Examining the Real‐Life Journey of Individuals and Families Affected by Single‐Ventricle Congenital Heart Disease

por Mery, Carlos M., Well, Andrew, Taylor, Kate, Carberry, Kathleen, Colucci, José, Ulack, Christopher, Zeiner, Adam, Mizrahi, Michelle, Stewart, Eileen, Dillingham, Christine, Cook, Taylor, Hartounian, Arotin, McCullum, Elizabeth, Affolter, Jeremy T., Van Diest, Heather, Lamari‐Fisher, Alexandra, Chang, Stacey, Wallace, Scott, Teisberg, Elizabeth, Fraser, Charles D.
Publicado 2023

Physician Self-assessment of Shared Decision-making in Simulated Intensive Care Unit Family Meetings

por Vasher, Scott T., Oppenheim, Ian M., Sharma Basyal, Pragyashree, Lee, Emma M., Hayes, Margaret M., Turnbull, Alison E.
Publicado 2020

Birth Outcomes in DES Children and Grandchildren: A Multigenerational National Cohort Study on Informative Families

por Gaspari, Laura, Soyer-Gobillard, Marie-Odile, Rincheval, Nathalie, Paris, Françoise, Kalfa, Nicolas, Hamamah, Samir, Sultan, Charles
Publicado 2023

Outcomes of surgical management of familial intrahepatic cholestasis 1 and bile salt export protein deficiencies

por Bull, Laura N., Pawlikowska, Ludmila, Strautnieks, Sandra, Jankowska, Irena, Czubkowski, Piotr, Dodge, Jennifer L., Emerick, Karan, Wanty, Catherine, Wali, Sami, Blanchard, Samra, Lacaille, Florence, Byrne, Jane A., van Eerde, Albertien M., Kolho, Kaija‐Leena, Houwen, Roderick, Lobritto, Steven, Hupertz, Vera, McClean, Patricia, Mieli‐Vergani, Giorgina, Sokal, Etienne, Rosenthal, Philip, Whitington, Peter F., Pawlowska, Joanna, Thompson, Richard J.
Publicado 2018

Integration of Catholic Values and Professional Obligations in the Provision of Family Planning Services: A Qualitative Study

por Marchin, Angela, Seale, Rebecca, Sheeder, Jeanelle, Teal, Stephanie, Guiahi, Maryam
Publicado 2020

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

por Oliver, Karen L., Ellis, Colin A., Scheffer, Ingrid E., Ganesan, Shiva, Leu, Costin, Sadleir, Lynette G., Heinzen, Erin L., Mefford, Heather C., Bass, Andrew J., Curtis, Sarah W., Harris, Rebekah V., Whiteman, David C., Helbig, Ingo, Ottman, Ruth, Epstein, Michael P., Bahlo, Melanie, Berkovic, Samuel F.
Publicado 2022

Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia

por Dijk, Wieneke, Di Filippo, Mathilde, Kooijman, Sander, van Eenige, Robin, Rimbert, Antoine, Caillaud, Amandine, Thedrez, Aurélie, Arnaud, Lucie, Pronk, Amanda, Garçon, Damien, Sotin, Thibaud, Lindenbaum, Pierre, Ozcariz Garcia, Enrique, Pais de Barros, Jean-Paul, Duvillard, Laurence, Si-Tayeb, Karim, Amigo, Nuria, Le Questel, Jean-Yves, Rensen, Patrick C.N., Le May, Cédric, Moulin, Philippe, Cariou, Bertrand
Publicado 2022

Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia

por Iacocca, Michael A., Wang, Jian, Dron, Jacqueline S., Robinson, John F., McIntyre, Adam D., Cao, Henian, Hegele, Robert A.
Publicado 2017

Family Conferences to Facilitate Deprescribing in Older Outpatients With Frailty and With Polypharmacy: The COFRAIL Cluster Randomized Trial

por Mortsiefer, Achim, Löscher, Susanne, Pashutina, Yekaterina, Santos, Sara, Altiner, Attila, Drewelow, Eva, Ritzke, Manuela, Wollny, Anja, Thürmann, Petra, Bencheva, Veronika, Gogolin, Matthias, Meyer, Gabriele, Abraham, Jens, Fleischer, Steffen, Icks, Andrea, Montalbo, Joseph, Wiese, Birgitt, Wilm, Stefan, Feldmeier, Gregor
Publicado 2023

Effect of Longer Family Meals on Children’s Fruit and Vegetable Intake: A Randomized Clinical Trial

por Dallacker, Mattea, Knobl, Vanessa, Hertwig, Ralph, Mata, Jutta
Publicado 2023

Modeling the Inactivation of Viruses from the Coronaviridae Family in Response to Temperature and Relative Humidity in Suspensions or on Surfaces

por Guillier, Laurent, Martin-Latil, Sandra, Chaix, Estelle, Thébault, Anne, Pavio, Nicole, Le Poder, Sophie, Batéjat, Christophe, Biot, Fabrice, Koch, Lionel, Schaffner, Donald W., Sanaa, Moez
Publicado 2020

Investigating the Diversity and Host Range of Novel Parvoviruses from North American Ducks Using Epidemiology, Phylogenetics, Genome Structure, and Codon Usage Analysis

por Canuti, Marta, Verhoeven, Joost T. P., Munro, Hannah J., Roul, Sheena, Ojkic, Davor, Robertson, Gregory J., Whitney, Hugh G., Dufour, Suzanne C., Lang, Andrew S.
Publicado 2021

The Effect of Improved Access to Family Planning on Postpartum Women: Protocol for a Randomized Controlled Trial

por Karra, Mahesh, Canning, David
Publicado 2020

Deregulation and epigenetic modification of BCL2-family genes cause resistance to venetoclax in hematologic malignancies

por Thomalla, D., Beckmann, L., Grimm, C., Oliverio, M., Meder, L., Herling, C.D., Nieper, P., Feldmann, T., Merkel, O., Lorsy, E., da Palma Guerreiro, A., von Jan, J., Kisis, I., Wasserburger, E., Claasen, J., Faitschuk-Meyer, E., Altmüller, J., Nürnberg, P., Yang, T.-P., Lienhard, M., Herwig, R., Kreuzer, K.-A., Pallasch, C.P., Büttner, R., Schäfer, S.C., Hartley, J., Abken, H., Peifer, M., Kashkar, H., Knittel, G., Eichhorst, B., Ullrich, R.T., Herling, M., Reinhardt, H.C., Hallek, M., Schweiger, M.R., Frenzel, L.P.
Publicado 2022

The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review

por Vo, Oanh Kieu, McNeill, Alisdair, Vogt, Katharina Sophie
Publicado 2018

Hepatic copper accumulation in a young cat with familial variations in the ATP7B gene

por Asada, Hajime, Kojima, Mari, Nagahara, Takuro, Goto‐Koshino, Yuko, Chambers, James K., Nakagawa, Taisuke, Yokoyama, Nozomu, Uchida, Kazuyuki, Tsujimoto, Hajime, Ohno, Koichi
Publicado 2018

Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosis

por Yang, Yi, Zhang, Lei, Lynch, David R., Lukas, Thomas, Ahmeti, Kreshnik, Sleiman, Patrick M.A., Ryan, Eanna, Schadt, Kimberly A., Newman, Jordan H., Deng, Han-Xiang, Siddique, Nailah, Siddique, Teepu
Publicado 2016

Health-Related Quality of Life in Adults From 17 Family Practice Clinics in North Carolina

por Callahan, Leigh F., Shreffler, Jack, Mielenz, Thelma J., Kaufman, Jay S., Schoster, Britta, Randolph, Randy, Sloane, Philip, DeVellis, Robert, Weinberger, Morris
Publicado 2008

A familial natural short sleep mutation promotes healthy aging and extends lifespan in Drosophila

por Pandey, Pritika, Wall, P. Kerr, Lopez, Stephen R., Dubuisson, Olga S., Zunica, Elizabeth R.M., Dantas, Wagner S., Kirwan, John P., Axelrod, Christopher L., Johnson, Alyssa E.
Publicado 2023

Developing a second-generation clinical candidate AAV vector for gene therapy of familial hypercholesterolemia

por Wang, Lili, Muthuramu, Ilayaraja, Somanathan, Suryanarayan, Zhang, Hong, Bell, Peter, He, Zhenning, Yu, Hongwei, Zhu, Yanqing, Tretiakova, Anna P., Wilson, James M.
Publicado 2021