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

N-formyl methionine peptide-driven neutrophil activation in idiopathic inflammatory myopathies

N-甲酰甲硫氨酸肽驱动的中性粒细胞活化在特发性炎症性肌病中的作用

Gonzalez-Chapa, Jorge A; Horuluoglu, Begum; Notarnicola, Antonella; Rathee, Arpit; Kaur, Noor; Stultz, Ryan D; Christopher-Stine, Lisa; Albayda, Jemima; Nennesmo, Inger; Lundberg, Ingrid E; Lood, Christian

Acquired Multiple Acyl-Coenzyme A Dehydrogenase Deficiency Associated With Sertraline in Sweden-A Nationwide Population-Based Study

瑞典一项基于全国人口的研究:舍曲林相关获得性多酰基辅酶A脱氢酶缺乏症

Sunebo, Sofie; Nilsson, Emil; Engvall, Martin; Hedberg-Oldfors, Carola; Shen, Yan; Nennesmo, Inger; Danielsson, Olof; Oldfors, Anders; Appelqvist, Hanna; Lindgren, Ulrika

The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder

ZFHX3 GGC 重复序列扩增是 4 型脊髓小脑性共济失调的根本原因,它具有共同的祖先。

Chen, Zhongbo; Alvarez Jerez, Pilar; Anderson, Claire; Paucar, Martin; Lee, Jasmaine; Nilsson, Daniel; Macpherson, Hannah; Scardamaglia, Annarita; Montgomery, Kylie; Hardy, John; Singleton, Andrew B; Tucci, Arianna; Mathews, Katherine D; Fu, Ying-Hui; Engvall, Martin; Laffita-Mesa, José; Nennesmo, Inger; Wedell, Anna; Ptáček, Louis J; Blauwendraat, Cornelis; Gustavsson, Emil K; Svenningsson, Per; Ryten, Mina; Houlden, Henry

Phenotypic variability in early-onset dementia segregating with a novel APP (p.I718M) variant

早发性痴呆的表型变异与一种新的APP(p.I718M)变异相关

Johansson, Charlotte; Rodriguez-Vieitez, Elena; Bluma, Marina; Nennesmo, Inger; Thonberg, Håkan; Ullgren, Abbe; Jelic, Vesna; Zetterberg, Henrik; Blennow, Kaj; Nordberg, Agneta; Graff, Caroline

Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

作者更正:一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

Ehn, Emma; Eisfeldt, Jesper; Laffita-Mesa, Jose M; Thonberg, Håkan; Schoumans, Jacqueline; Portaankorva, Anne M; Viitanen, Matti; Lindstrand, Anna; Nennesmo, Inger; Graff, Caroline

A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

一种新生、嵌合且复杂的21号染色体重排导致APP三倍体和家族性常染色体显性遗传早发性阿尔茨海默病。

Ehn, Emma; Eisfeldt, Jesper; Laffita-Mesa, Jose M; Thonberg, Håkan; Schoumans, Jacqueline; Portaankorva, Anne M; Viitanen, Matti; Lindstrand, Anna; Nennesmo, Inger; Graff, Caroline

Immune Characterization of a Vietnamese Cohort With Idiopathic Inflammatory Myopathies.

越南特发性炎症性肌病患者队列的免疫特征分析

Luo Yue-Bei, Nakazawa Maho, Minh Nham Pham Thi, Heinon Léo, Nennesmo Inger, Rönnelid Johan, Lundberg Ingrid E, Phuong Thuy Nguyen Thi, Horuluoglu Begum

Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3

与 XPNPEP3 基因中一种新的纯合变异相关的伴有听力丧失和肾痨的共济失调综合征

Ben-Shabat, Ilan; Kvarnung, Malin; Sperker, Wolfgang; Bruhn, Helene; Wredenberg, Anna; Wibom, Rolf; Nennesmo, Inger; Engvall, Martin; Paucar, Martin

Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease

创建皮克氏病国际联盟:MAPT H2 单倍型与皮克氏病风险的关联研究

Valentino, Rebecca R; Scotton, William J; Roemer, Shanu F; Lashley, Tammaryn; Heckman, Michael G; Shoai, Maryam; Martinez-Carrasco, Alejandro; Tamvaka, Nicole; Walton, Ronald L; Baker, Matthew C; Macpherson, Hannah L; Real, Raquel; Soto-Beasley, Alexandra I; Mok, Kin; Revesz, Tamas; Warner, Thomas T; Jaunmuktane, Zane; Boeve, Bradley F; Christopher, Elizabeth A; DeTure, Michael; Duara, Ranjan; Graff-Radford, Neill R; Josephs, Keith A; Knopman, David S; Koga, Shunsuke; Murray, Melissa E; Lyons, Kelly E; Pahwa, Rajesh; Parisi, Joseph E; Petersen, Ronald C; Whitwell, Jennifer; Grinberg, Lea T; Miller, Bruce; Schlereth, Athena; Seeley, William W; Spina, Salvatore; Grossman, Murray; Irwin, David J; Lee, Edward B; Suh, EunRan; Trojanowski, John Q; Van Deerlin, Vivianna M; Wolk, David A; Connors, Theresa R; Dooley, Patrick M; Frosch, Matthew P; Oakley, Derek H; Aldecoa, Iban; Balasa, Mircea; Gelpi, Ellen; Borrego-Écija, Sergi; de Eugenio Huélamo, Rosa Maria; Gascon-Bayarri, Jordi; Sánchez-Valle, Raquel; Sanz-Cartagena, Pilar; Piñol-Ripoll, Gerard; Molina-Porcel, Laura; Bigio, Eileen H; Flanagan, Margaret E; Gefen, Tamar; Rogalski, Emily J; Weintraub, Sandra; Redding-Ochoa, Javier; Chang, Koping; Troncoso, Juan C; Prokop, Stefan; Newell, Kathy L; Ghetti, Bernardino; Jones, Matthew; Richardson, Anna; Robinson, Andrew C; Roncaroli, Federico; Snowden, Julie; Allinson, Kieren; Green, Oliver; Rowe, James B; Singh, Poonam; Beach, Thomas G; Serrano, Geidy E; Flowers, Xena E; Goldman, James E; Heaps, Allison C; Leskinen, Sandra P; Teich, Andrew F; Black, Sandra E; Keith, Julia L; Masellis, Mario; Bodi, Istvan; King, Andrew; Sarraj, Safa-Al; Troakes, Claire; Halliday, Glenda M; Hodges, John R; Kril, Jillian J; Kwok, John B; Piguet, Olivier; Gearing, Marla; Arzberger, Thomas; Roeber, Sigrun; Attems, Johannes; Morris, Christopher M; Thomas, Alan J; Evers, Bret M; White, Charles L; Mechawar, Naguib; Sieben, Anne A; Cras, Patrick P; De Vil, Bart B; De Deyn, Peter Paul P P; Duyckaerts, Charles; Le Ber, Isabelle; Seihean, Danielle; Turbant-Leclere, Sabrina; MacKenzie, Ian R; McLean, Catriona; Cykowski, Matthew D; Ervin, John F; Wang, Shih-Hsiu J; Graff, Caroline; Nennesmo, Inger; Nagra, Rashed M; Riehl, James; Kovacs, Gabor G; Giaccone, Giorgio; Nacmias, Benedetta; Neumann, Manuela; Ang, Lee-Cyn; Finger, Elizabeth C; Blauwendraat, Cornelis; Nalls, Mike A; Singleton, Andrew B; Vitale, Dan; Cunha, Cristina; Carvalho, Agostinho; Wszolek, Zbigniew K; Morris, Huw R; Rademakers, Rosa; Hardy, John A; Dickson, Dennis W; Rohrer, Jonathan D; Ross, Owen A

Astroglial tracer BU99008 detects multiple binding sites in Alzheimer's disease brain

星形胶质细胞示踪剂BU99008可检测阿尔茨海默病脑组织中的多个结合位点。

Kumar, Amit; Koistinen, Niina A; Malarte, Mona-Lisa; Nennesmo, Inger; Ingelsson, Martin; Ghetti, Bernardino; Lemoine, Laetitia; Nordberg, Agneta