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

Classification of Alzheimer's Disease and Frontotemporal Dementia Using Electroencephalography to Quantify Communication between Electrode Pairs

利用脑电图量化电极对间通讯对阿尔茨海默病和额颞叶痴呆进行分类

Ma, Yuan; Bland, Jeffrey Keith Spaneas; Fujinami, Tsutomu

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients

全外显子组测序为肾移植受者实现精准医疗提供了可能

Mann, Nina; Braun, Daniela A; Amann, Kassaundra; Tan, Weizhen; Shril, Shirlee; Connaughton, Dervla M; Nakayama, Makiko; Schneider, Ronen; Kitzler, Thomas M; van der Ven, Amelie T; Chen, Jing; Ityel, Hadas; Vivante, Asaf; Majmundar, Amar J; Daga, Ankana; Warejko, Jillian K; Lovric, Svjetlana; Ashraf, Shazia; Jobst-Schwan, Tilman; Widmeier, Eugen; Hugo, Hannah; Mane, Shrikant M; Spaneas, Leslie; Somers, Michael J G; Ferguson, Michael A; Traum, Avram Z; Stein, Deborah R; Baum, Michelle A; Daouk, Ghaleb H; Lifton, Richard P; Manzi, Shannon; Vakili, Khashayar; Kim, Heung Bae; Rodig, Nancy M; Hildebrandt, Friedhelm

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

全外显子组测序可识别出患有先天性肾脏和泌尿系统畸形家族的致病突变

van der Ven, Amelie T; Connaughton, Dervla M; Ityel, Hadas; Mann, Nina; Nakayama, Makiko; Chen, Jing; Vivante, Asaf; Hwang, Daw-Yang; Schulz, Julian; Braun, Daniela A; Schmidt, Johanna Magdalena; Schapiro, David; Schneider, Ronen; Warejko, Jillian K; Daga, Ankana; Majmundar, Amar J; Tan, Weizhen; Jobst-Schwan, Tilman; Hermle, Tobias; Widmeier, Eugen; Ashraf, Shazia; Amar, Ali; Hoogstraaten, Charlotte A; Hugo, Hannah; Kitzler, Thomas M; Kause, Franziska; Kolvenbach, Caroline M; Dai, Rufeng; Spaneas, Leslie; Amann, Kassaundra; Stein, Deborah R; Baum, Michelle A; Somers, Michael J G; Rodig, Nancy M; Ferguson, Michael A; Traum, Avram Z; Daouk, Ghaleb H; Bogdanović, Radovan; Stajić, Natasa; Soliman, Neveen A; Kari, Jameela A; El Desoky, Sherif; Fathy, Hanan M; Milosevic, Danko; Al-Saffar, Muna; Awad, Hazem S; Eid, Loai A; Selvin, Aravind; Senguttuvan, Prabha; Sanna-Cherchi, Simone; Rehm, Heidi L; MacArthur, Daniel G; Lek, Monkol; Laricchia, Kristen M; Wilson, Michael W; Mane, Shrikant M; Lifton, Richard P; Lee, Richard S; Bauer, Stuart B; Lu, Weining; Reutter, Heiko M; Tasic, Velibor; Shril, Shirlee; Hildebrandt, Friedhelm

Prevalence of Monogenic Causes in Pediatric Patients with Nephrolithiasis or Nephrocalcinosis

儿童肾结石或肾钙质沉着症中单基因病因的患病率

Braun, Daniela Anne; Lawson, Jennifer Ashley; Gee, Heon Yung; Halbritter, Jan; Shril, Shirlee; Tan, Weizhen; Stein, Deborah; Wassner, Ari J; Ferguson, Michael A; Gucev, Zoran; Fisher, Brittany; Spaneas, Leslie; Varner, Jennifer; Sayer, John A; Milosevic, Danko; Baum, Michelle; Tasic, Velibor; Hildebrandt, Friedhelm

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis

14个单基因基因占肾结石/肾钙质沉着症的15%。

Halbritter, Jan; Baum, Michelle; Hynes, Ann Marie; Rice, Sarah J; Thwaites, David T; Gucev, Zoran S; Fisher, Brittany; Spaneas, Leslie; Porath, Jonathan D; Braun, Daniela A; Wassner, Ari J; Nelson, Caleb P; Tasic, Velibor; Sayer, John A; Hildebrandt, Friedhelm

Short sirolimus half-life in pediatric renal transplant recipients on a calcineurin inhibitor-free protocol

在接受无钙调神经磷酸酶抑制剂方案治疗的儿科肾移植受者中,西罗莫司半衰期较短。

Schachter, Asher D; Meyers, K E; Spaneas, L D; Palmer, J A; Salmanullah, M; Baluarte, J; Brayman, K L; Harmon, W E