日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The potential clinical and public health implications of presymptomatic genetic testing for transthyretin amyloidosis in African American/Black adults in the United States

美国非裔美国人/黑人成年人中,转甲状腺素蛋白淀粉样变性无症状基因检测的潜在临床和公共卫生意义

Bharaj, Inderjeet; Singh, Simar J; Munaim, Juzer; Grewal, Harneet; Sabrowsky, Sonia; Boshara, Andrew; Silver, Marc A; Brendish, Katherine H; Underwood, Paul; Dev, Sandesh; Osundiji, Mayowa A

Development and external validation of a mixed-reality aneurysm clipping simulator

混合现实动脉瘤夹闭模拟器的开发和外部验证

Gmeiner, Matthias; Schrempf, Andreas; Thurner, Thomas; Fenz, Wolfgang; Sabrowsky-Hirsch, Bertram; Giretzlehner, Michael; Prückl, Robert; Schaffelhofer, Stefan; Major, Zoltan; Lämmermann, Sebastian; Baumgartner, Melanie; Drabauer, Lukas; Nagy, Jozsef; Esposito, Giuseppe; Colombo, Elisa; Stroh-Holly, Nico; Gruber, Andreas

Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

更正:在三级医疗保健系统中实施罕见病基因组医学:梅奥诊所罕见病和未确诊疾病项目 (PRaUD)

Pinto E Vairo, Filippo; Kemppainen, Jennifer L; Vitek, Carolyn R Rohrer; Whalen, Denise A; Kolbert, Kayla J; Sikkink, Kaitlin J; Kroc, Sarah A; Kruisselbrink, Teresa; Shupe, Gabrielle F; Knudson, Alyssa K; Burke, Elizabeth M; Loftus, Elle C; Bandel, Lorelei A; Prochnow, Carri A; Mulvihill, Lindsay A; Thomas, Brittany; Gable, Dale M; Graddy, Courtney B; Garzon, Giovanna G Moreno; Ekpoh, Idara U; Porquera, Eva M Carmona; Fervenza, Fernando C; Hogan, Marie C; El Ters, Mireille; Warrington, Kenneth J; Davis, John M 3rd; Koster, Matthew J; Orandi, Amir B; Basiaga, Matthew L; Vella, Adrian; Kumar, Seema; Creo, Ana L; Lteif, Aida N; Pittock, Siobhan T; Tebben, Peter J; Abate, Ejigayehu G; Joshi, Avni Y; Ristagno, Elizabeth H; Patnaik, Mrinal S; Schimmenti, Lisa A; Dhamija, Radhika; Sabrowsky, Sonia M; Wierenga, Klaas J; Keddis, Mira T; Samadder, Niloy Jewel J; Presutti, Richard J; Robinson, Steven I; Stephens, Michael C; Roberts, Lewis R; Faubion, William A Jr; Driscoll, Sherilyn W; Wong-Kisiel, Lily C; Selcen, Duygu; Flanagan, Eoin P; Ramanan, Vijay K; Jackson, Lauren M; Mauermann, Michelle L; Ortega, Victor E; Anderson, Sarah A; Aoudia, Stacy L; Klee, Eric W; McAllister, Tammy M; Lazaridis, Konstantinos N

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

在三级医疗保健系统中实施基因组医学治疗罕见病:梅奥诊所罕见病和未确诊疾病项目 (PRaUD)

Pinto E Vairo, Filippo; Kemppainen, Jennifer L; Vitek, Carolyn R Rohrer; Whalen, Denise A; Kolbert, Kayla J; Sikkink, Kaitlin J; Kroc, Sarah A; Kruisselbrink, Teresa; Shupe, Gabrielle F; Knudson, Alyssa K; Burke, Elizabeth M; Loftus, Elle C; Bandel, Lorelei A; Prochnow, Carri A; Mulvihill, Lindsay A; Thomas, Brittany; Gable, Dale M; Graddy, Courtney B; Garzon, Giovanna G Moreno; Ekpoh, Idara U; Porquera, Eva M Carmona; Fervenza, Fernando C; Hogan, Marie C; El Ters, Mireille; Warrington, Kenneth J; Davis, John M 3rd; Koster, Matthew J; Orandi, Amir B; Basiaga, Matthew L; Vella, Adrian; Kumar, Seema; Creo, Ana L; Lteif, Aida N; Pittock, Siobhan T; Tebben, Peter J; Abate, Ejigayehu G; Joshi, Avni Y; Ristagno, Elizabeth H; Patnaik, Mrinal S; Schimmenti, Lisa A; Dhamija, Radhika; Sabrowsky, Sonia M; Wierenga, Klaas J; Keddis, Mira T; Samadder, Niloy Jewel J; Presutti, Richard J; Robinson, Steven I; Stephens, Michael C; Roberts, Lewis R; Faubion, William A Jr; Driscoll, Sherilyn W; Wong-Kisiel, Lily C; Selcen, Duygu; Flanagan, Eoin P; Ramanan, Vijay K; Jackson, Lauren M; Mauermann, Michelle L; Ortega, Victor E; Anderson, Sarah A; Aoudia, Stacy L; Klee, Eric W; McAllister, Tammy M; Lazaridis, Konstantinos N