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

The VASCERN-VASCA diagnostic and management pathways for kaposiform hemangioendothelioma

卡波西样血管内皮瘤的VASCERN-VASCA诊断和管理路径

Gasparella, Paolo; Haxhija, Emir Q; Andersen, Rune; Barea, Maria; Baselga, Eulalia; Serrano, Miguel Bejarano; Berger, Sigurd; Bisdorff, Annouk Anne; Boccara, Olivia; Borgards, Petra; Bom-Sucesso, Maria; Boon, Laurence M; Cimpean, Anca Maria; Diociaiuti, Andrea; Dvorakova, Veronika; Hachem, May El; Frisk, Sofia; Ghaffarpour, Nader; Holm, Annegret; Irvine, Alan D; Kaltoft, Mikkel; Kapp, Friedrich G; Koskova, Olga; Kyrklund, Kristiina; Madureira, Miguel; Palionis, Darius; Przewratil, Przemysław; Schönewolf-Greulich, Bitten; Stanciulescu, Maria-Corina; Štěrba, Jaroslav; Tolonen, Jukka; Vaisnyte, Birute; van der Vleuten, Carine; Wyrzykowski, Dariusz; Kool, Leo Schultze; Vikkula, Miikka

Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

VASCERN-VASCA对血管异常中体细胞变异的基因-疾病关联进行评估并提出基因检测建议

Revencu, Nicole; Eijkelenboom, Astrid; Bracquemart, Claire; Alhopuro, Pia; Armstrong, Judith; Baselga, Eulalia; Cesario, Claudia; Dentici, Maria Lisa; Eyries, Melanie; Frisk, Sofia; Karstensen, Helena Gásdal; Gene-Olaciregui, Nagore; Kivirikko, Sirpa; Lavarino, Cinzia; Mero, Inger-Lise; Michiels, Rodolphe; Pisaneschi, Elisa; Schönewolf-Greulich, Bitten; Wieland, Ilse; Zenker, Martin; Vikkula, Miikka

Correction to: Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

更正:VASCERN-VASCA 对血管畸形体细胞变异的基因-疾病关联评估及基因检测建议

Revencu, Nicole; Eijkelenboom, Astrid; Bracquemart, Claire; Alhopuro, Pia; Armstrong, Judith; Baselga, Eulalia; Cesario, Claudia; Dentici, Maria Lisa; Eyries, Melanie; Frisk, Sofia; Karstensen, Helena Gásdal; Gene-Olaciregui, Nagore; Kivirikko, Sirpa; Lavarino, Cinzia; Mero, Inger-Lise; Michiels, Rodolphe; Pisaneschi, Elisa; Schönewolf-Greulich, Bitten; Wieland, Ilse; Zenker, Martin; Vikkula, Miikka

Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations

由新的 GFM1 突变引起的新生儿线粒体肝性脑病

Kirstine Ravn, Bitten Schönewolf-Greulich, Rikke M Hansen, Anna-Helene Bohr, Morten Duno, Flemming Wibrand, Elsebet Ostergaard