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

Frequency and short-term persistence of haematuria and/or proteinuria in neonates: a cohort study

新生儿血尿和/或蛋白尿的发生率及短期持续时间:一项队列研究

Kittel, Jochen; Seilbeck, Christine; Brandstetter, Susanne; Kabesch, Michael; Melter, Michael; Köninger, Angela; Apfelbacher, Christian; Ambrosch, Andreas; Geis, Tobias

Spectrum of Clinical and Imaging Features of Children With GFAP Astrocytopathy

GFAP星形胶质细胞病患儿的临床和影像学特征谱

Sommer, Simon; Panzer, Andreas; Bertolini, Annikki; Cleaveland, Robert; Jain, Vivek; Kapanci, Tugba; Derichs, Ute; Geis, Tobias; Neu, Axel; Löhr-Nilles, Christa; Aeschimann-Huhn, Rahel; Flotats-Bastardas, Marina; Deiva, Kumaran; Armangue, Thais; Olivé-Cirera, Gemma; Kannoth, Sudheeran; Koy, Anne; Meirson, Hadas; Fattal-Valevski, Aviva; Ganelin-Cohen, Esther; Losch, Heike; Horne, Annacarin; Wickström, Ronny; Dargvainiene, Justina; Leypoldt, Frank; Rostasy, Kevin

The Two Faces of Pediatric SCA2

儿童SCA2的两面性

Rive Le Gouard, Nicolas; G Bah, Maissa; Coarelli, Giulia; Heinzmann, Anna; Fauret, Anne-Laure; de Sainte-Agathe, Jean-Madeleine; Cazeneuve, Cécile; Gerasimenko, Anna; Gras, Domitille; Capri, Yline; Renaud, Mathilde; Brais, Bernard; Grenenko, Cecile; Masurel, Alice; Berquin, Patrick; Jobic, Florence; Métreau, Julia; Deiva, Kumaran; Afenjar, Alexandra; Gravrand, Victor; Lannuzel, Annie; Anheim, Mathieu; Geis, Tobias; Hehr, Ute; Madan Cohen, Jennifer; Desnous, Béatrice; J A Kievit, Anneke; Bahi-Buisson, Nadia; Rodriguez, Diana; Renaldo, Florence; Cances, Claude; Devos, David; Angelini, Chloé; Goizet, Cyril; Ewenczyk, Claire; Durr, Alexandra; Mignot, Cyril

Neurofilament Light Chain as Biomarker in Encephalitis

神经丝轻链作为脑炎的生物标志物

Wellmann, Sven; Geis, Tobias; Kuhle, Jens; Lehnerer, Verena

Neurofilament Light Chain Concentration in Cerebrospinal Fluid in Children with Acute Nontraumatic Neurological Disorders

急性非创伤性神经系统疾病患儿脑脊液中神经丝轻链浓度

Geis, Tobias; Gutzeit, Svena; Disse, Sigrid; Kuhle, Jens; Fouzas, Sotiris; Wellmann, Sven

Ketogenic Diet Treatment of Defects in the Mitochondrial Malate Aspartate Shuttle and Pyruvate Carrier.

生酮饮食治疗线粒体苹果酸天冬氨酸穿梭和丙酮酸载体缺陷

Bölsterli Bigna K, Boltshauser Eugen, Palmieri Luigi, Spenger Johannes, Brunner-Krainz Michaela, Distelmaier Felix, Freisinger Peter, Geis Tobias, Gropman Andrea L, Häberle Johannes, Hentschel Julia, Jeandidier Bruno, Karall Daniela, Keren Boris, Klabunde-Cherwon Annick, Konstantopoulou Vassiliki, Kottke Raimund, Lasorsa Francesco M, Makowski Christine, Mignot Cyril, O'Gorman Tuura Ruth, Porcelli Vito, Santer René, Sen Kuntal, Steinbrücker Katja, Syrbe Steffen, Wagner Matias, Ziegler Andreas, Zöggeler Thomas, Mayr Johannes A, Prokisch Holger, Wortmann Saskia B

Serum neurofilament light chain (sNfL) values in a large cross-sectional population of children with asymptomatic to moderate COVID-19

一项针对大量无症状至中度 COVID-19 儿童的横断面研究,检测了他们的血清神经丝轻链 (sNfL) 值。

Geis, Tobias; Brandstetter, Susanne; Toncheva, Antoaneta A; Laub, Otto; Leipold, Georg; Wagner, Ralf; Kabesch, Michael; Kasser, Severin; Kuhle, Jens; Wellmann, Sven

International consensus recommendations on the diagnostic work-up for malformations of cortical development

关于皮质发育畸形诊断流程的国际共识建议

Oegema, Renske; Barakat, Tahsin Stefan; Wilke, Martina; Stouffs, Katrien; Amrom, Dina; Aronica, Eleonora; Bahi-Buisson, Nadia; Conti, Valerio; Fry, Andrew E; Geis, Tobias; Andres, David Gomez; Parrini, Elena; Pogledic, Ivana; Said, Edith; Soler, Doriette; Valor, Luis M; Zaki, Maha S; Mirzaa, Ghayda; Dobyns, William B; Reiner, Orly; Guerrini, Renzo; Pilz, Daniela T; Hehr, Ute; Leventer, Richard J; Jansen, Anna C; Mancini, Grazia M S; Di Donato, Nataliya

Interval Timing in Pediatric Multiple Sclerosis: Impaired in the Subsecond Range but Unimpaired in the One-Second Range

儿童多发性硬化症患者的时间间隔感知能力:亚秒级受损,但一秒级正常

Troche, Stefan J; Kapanci, Tugba; Rammsayer, Thomas H; Kesseler, Carl P A; Häusler, Martin Georg; Geis, Tobias; Schimmel, Mareike; Elpers, Christiane; Kreth, Jonas H; Thiels, Charlotte; Rostásy, Kevin

Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders

一项针对27个POMT1相关疾病家族的队列研究,探讨了临床长期病程、新发现的突变以及基因型-表型相关性。

Geis, Tobias; Rödl, Tanja; Topaloğlu, Haluk; Balci-Hayta, Burcu; Hinreiner, Sophie; Müller-Felber, Wolfgang; Schoser, Benedikt; Mehraein, Yasmin; Hübner, Angela; Zirn, Birgit; Hoopmann, Markus; Reutter, Heiko; Mowat, David; Schuierer, Gerhard; Schara, Ulrike; Hehr, Ute; Kölbel, Heike