Zobrazeno 1 - 10
of 964
pro vyhledávání: '"L. Wenger"'
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-10 (2023)
Abstract Background Sandplay therapy is a psychotherapeutic technique, based on the psychoanalytic theory of the unconscious. Nearly a century after it was developed, sandplay can now be applied for the initial diagnosis tools for sand players. The g
Externí odkaz:
https://doaj.org/article/c804738ecd1a4fe1ace11f53e7b859ca
Autor:
A. L. Wenger, Muhamed Barakovic, Sara Bosticardo, Sabine Schaedelin, Alessandro Daducci, Simona Schiavi, Matthias Weigel, Reza Rahmanzadeh, Po-Jui Lu, Alessandro Cagol, Ludwig Kappos, Jens Kuhle, Pasquale Calabrese, Cristina Granziera
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionThe presence of focal cortical and white matter damage in patients with multiple sclerosis (pwMS) might lead to specific alterations in brain networks that are associated with cognitive impairment. We applied microstructure-weighted conne
Externí odkaz:
https://doaj.org/article/00b79015a65f42ae8270c6dafd774716
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundCOVID-19 epidemic has lasted for nearly 3 years, and revolutionized social life. In the study, in-depth interviews were conducted with Chinese undergraduate students to explore their understanding and experience of meaning in life. Meaning
Externí odkaz:
https://doaj.org/article/05dec88fa8664694b4394c4433def9e4
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2022)
BackgroundThe stigma of internet surfing is a relatively new area of study arising from the popularity of the internet. The Questionnaire on the Internal Stigma of Internet Surfing-9 (QISIS-9) was developed for the Chinese culture, so its suitability
Externí odkaz:
https://doaj.org/article/11950f11ae2e4569b3fd17cc78cbc8e8
Autor:
Prasanth Pattisapu, Tara L. Wenger, John P. Dahl, Randall A. Bly, Juliana Bonilla‐Velez, Natalie Wu, Anurekha Hall, Erin R. Rudzinski, Jonathan A. Perkins
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Describe a novel use for a kinase inhibitor, imatinib, in young children with a known activated somatic mutation in PDGFR‐beta. Two patients with infantile myofibromatosis treated with imatinib. Case description of evaluation, diagnosis an
Externí odkaz:
https://doaj.org/article/0c6e85b3ed0146039d401b4df5d9dd97
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
Background: The outbreak of COVID-19 has brought about radical changes in social life. The study focuses on a special group, Chinese undergraduate students with left-behind experiences. Specifically, the study addresses how such students feel and gra
Externí odkaz:
https://doaj.org/article/3a7e516e34d743f185059405d858388b
Autor:
Andrew T. Timberlake, Stephen McGee, Garrett Allington, Emre Kiziltug, Erin M. Wolfe, Amy L. Stiegler, Titus J. Boggon, May Sanyoura, Michelle Morrow, Tara L. Wenger, Erica M. Fernandes, Oana Caluseriu, John A. Persing, Sheng Chih Jin, Richard P. Lifton, Kristopher T. Kahle, Paul Kruszka
Publikováno v:
The American Journal of Human Genetics. 110:846-862
Autor:
Benjamin D. Solomon, Margaret P. Adam, Chin‐To Fong, Katta M. Girisha, Judith G. Hall, Anna C. E. Hurst, Peter M. Krawitz, Shahida Moosa, Shubha R. Phadke, Cedrik Tekendo‐Ngongang, Tara L. Wenger
Publikováno v:
American Journal of Medical Genetics Part A. 191:659-671
The field of clinical genetics and genomics continues to evolve. In the past few decades, milestones like the initial sequencing of the human genome, dramatic changes in sequencing technologies, and the introduction of artificial intelligence, have u
Autor:
Tara L. Wenger, Sheila Ganti, Catherine Bull, Erika Lutsky, James T. Bennett, Kaitlyn Zenner, Dana M. Jensen, Victoria Dmyterko, Ezgi Mercan, Giri M. Shivaram, Seth D. Friedman, Michael Bindschadler, Madeleine Drusin, Jonathan N. Perkins, Ada Kong, Randall A. Bly, John P. Dahl, Juliana Bonilla-Velez, Jonathan A. Perkins
Publikováno v:
Genetics in Medicine. 24:2318-2328
PIK3CA-related overgrowth spectrum (PROS) conditions of the head and neck are treatment challenges. Traditionally, these conditions require multiple invasive interventions, with incomplete malformation removal, disfigurement, and possible dysfunction
Autor:
Caitlin C. Clements, Tara L. Wenger, Alisa R. Zoltowski, Jennifer R. Bertollo, Judith S. Miller, Ashley B. de Marchena, Lauren M. Mitteer, John C. Carey, Benjamin E. Yerys, Elaine H. Zackai, Beverly S. Emanuel, Donna M. McDonald-McGinn, Robert T. Schultz
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-17 (2017)
Abstract Background Previous studies have reported no clear critical region for medical comorbidities in children with deletions or duplications of 22q11.2. The purpose of this study was to evaluate whether individuals with small nested deletions or
Externí odkaz:
https://doaj.org/article/e0920fdf03b84cc287869873723def41