Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Samuel Strom"'
Autor:
Giulliana Chávez-Pasco, Jeny Bazalar-Montoya, Cecilia Bonilla Suarez, Krista Bluske, Samuel Strom, Alka Malhotra, Becky Milewski, Erin Thorpe, Ryan Taft, Gioconda Manassero-Morales
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101262- (2024)
Externí odkaz:
https://doaj.org/article/365afadaa8a94fe88ff2857264cbc533
Autor:
Samuel Strom, Laura Amendola, Aditi Chawla, Vitor Onucic, Denise Perry, Akanchha Kesari, Ryan Taft
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101542- (2024)
Externí odkaz:
https://doaj.org/article/cb7824ee4db648958c2ef47f1f298109
Autor:
Laura Amendola, Alison Coffey, Samuel Strom, Akanchha Kesari, James Avecilla, Josh Lowry, Stetson Thacker, Julie Taylor, Kathryn Golden-Grant, Matt Brown, Becky Milewski, John Belmont, Denise Perry, Ryan Taft
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100467- (2023)
Externí odkaz:
https://doaj.org/article/29e7c281859140328181f6ddd9c992a4
Autor:
Alka Malhotra, Rueben Hejja, James Avecilla, Andrew Walker, Phillip Medrano, Felipe Mullen, Anusha Balusu, Pratyusha Vankayala, Maren Bennett, Aditi Chawla, Subramanian Ajay, Samuel Strom, Akanchha Kesari, Denise Perry, Ryan Taft
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100554- (2023)
Externí odkaz:
https://doaj.org/article/3a74723dafc349068a2a87bb8ebb95f0
Autor:
Kristen Sund, Samuel Strom, Pauline Fujita, Batsal Devkota, Jennifer Shah, Nathan Berkowitz, LeAnne Lovato, Elliott Margulies, Mitch Bekritsky
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100612- (2023)
Externí odkaz:
https://doaj.org/article/eb681f054be0478e9e495651c10d23f5
Autor:
Anthony J. Bleyer, Maggie Westemeyer, Jing Xie, Michelle S. Bloom, Katya Brossart, Jason J. Eckel, Frederick Jones, Miklos Z. Molnar, Wayne Kotzker, Prince Anand, Stanislav Kmoch, Yuan Xue, Samuel Strom, Sumit Punj, Zachary P. Demko, Hossein Tabriziani, Paul R. Billings, Trudy McKanna
Publikováno v:
Am J Nephrol
Introduction: Chronic kidney disease (CKD) is a major public health issue in the USA. Identification of monogenic causes of CKD, which are present in ∼10% of adult cases, can impact prognosis and patient management. Broad gene panels can provide un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4bb624c324a057cda64796a2ef916d4
https://pubmed.ncbi.nlm.nih.gov/35325889
https://pubmed.ncbi.nlm.nih.gov/35325889
Autor:
Lola Cook, Jeanine Schulze, Jennifer Verbrugge, James C. Beck, Karen S. Marder, Rachel Saunders-Pullman, Christine Klein, Anna Naito, Roy N. Alcalay, Alexis Brice, Amasi Kumeh, Andrew B. West, Andrew Singleton, Birgitt Schüle, Brian Fiske, Carolin Gabbert, Connie Marras, Cornelis Blauwendraat, Courtney Thaxton, Dario Alessi, David Craig, Edward A. Fon, Emily Forbes, Enza Maria Valente, Esther Sammler, Gill Chao, Giulietta Riboldi, Houda Zghal Elloumi, Ignacio Mata, Jamie C. Fong, Jean-Christophe Corvol, Joshua Shulman, Judith Peterschmitt, Karen Marder, Katja Lohmann, Kelly Nudelman, Lara Lange, Mark R. Cookson, Martha Nance, Matthew Farrer, Melina Grigorian, Michael A. Schwarzschild, Niccolo Mencacci, Owen Ross, Pramod Mistry, Priscila Hodges, Rachel Blake, S. Pablo Sardi, Sali Farhan, Samuel Strom, Shalini Padmanabhan, Shruthi Mohan, Simonne Longerich, Susanne Schneider, Suzanne Lesage, Tanya Bardakjian, Tatiana Foroud, Thomas Courtin, Thomas Tropea, Yunlong Liu, Ziv Gan-Or, Ali S. Shalash, Anne Hall, Avner Thaler, Carolyn M. Sue, Deborah Mascalzoni, Deborah Raymond, Emilia Mabel Gatto, Gian D. Pal, Inke König, Ivana Novakovic, Marcelo Merello, Mehri Salari, Niccolo Emanuele Mencacci, Nobutaka Hattori, Oksana Suchowersky, Soraya Bardien, Sun Ju Chung, Tatyana Simuni, Timothy Lynch, Vincenzo Bonifati
Publikováno v:
Parkinsonism Relat Disord
Parkinsonism and Related Disorders, 92, 107-111. Elsevier
Parkinsonism and Related Disorders, 92, 107-111. Elsevier
Introduction There have been no specific guidelines regarding which genes should be tested in the clinical setting for Parkinson's disease (PD) or parkinsonism. We evaluated the types of clinical genetic testing offered for PD as the first step of ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::795bfd2d4987b04ddddc4b213b2371ba
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-468461
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-468461
Autor:
Kathleen Keatley, Samuel Stromei-Cleroux, Tammy Wiltshire, Nina Rajala, Gary Burton, William V. Holt, D. Timothy J. Littlewood, Andrew G. Briscoe, Josephine Jung, Keyoumars Ashkan, Simon J. Heales, Geoffrey J. Pilkington, Brigitte Meunier, John E. McGeehan, Iain P. Hargreaves, Rhiannon E. McGeehan
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 13, p 3364 (2019)
Glioblastoma is the most common and malignant primary brain tumour in adults, with a dismal prognosis. This is partly due to considerable inter- and intra-tumour heterogeneity. Changes in the cellular energy-producing mitochondrial respiratory chain
Externí odkaz:
https://doaj.org/article/0099cc077a444987ab0fa88885d12c8e