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Page 1
Efficacy and safety of larotrectinib in TRK fusion-positive primary central nervous system tumors.
Neuro Oncol. 2022 Jun 1;24(6):997-1007. doi: 10.1093/neuonc/noab274.
Neuro Oncol. 2022.
PMID: 34850167
Free PMC article.
Clinical Trial.
Pediatric Patients with Stage IV Rhabdomyosarcoma Significantly Benefit from Long-Term Maintenance Therapy: Results of the CWS-IV 2002 and the CWS DOK IV 2004-Trials.
Tramsen L, Bochennek K, Sparber-Sauer M, Salzmann-Manrique E, Scheer M, Dantonello T, Borkhardt A, Dirksen U, Thorwarth A, Greiner J, Ebinger M, Weclawek-Tompol J, Ladenstein R, Ljungman G, Hallmen E, Lehrnbecher T, Koscielniak E, Klingebiel T.
Tramsen L, et al. Among authors: thorwarth a.
Cancers (Basel). 2023 Mar 30;15(7):2050. doi: 10.3390/cancers15072050.
Cancers (Basel). 2023.
PMID: 37046711
Free PMC article.
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Genomic Evolution and Personalized Therapy of an Infantile Fibrosarcoma Harboring an NTRK Oncogenic Fusion.
Thorwarth A, Haase K, Röefzaad C, Pajtler KW, Schramm K, Hauptmann K, Behnke A, Vokuhl C, Elgeti T, Gratopp A, Schulte JH, Scheer M, Hernáiz Driever P, Nysom K, Eggert A, Henssen AG, Deubzer HE.
Thorwarth A, et al.
JCO Precis Oncol. 2022 May;6:e2100283. doi: 10.1200/PO.21.00283.
JCO Precis Oncol. 2022.
PMID: 35613412
Free PMC article.
No abstract available.
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Germline Mutations Including the Rare Pathogenic Variant c.3206delC in the ATM Gene Cause Ataxia Teleangiectasia-Associated Primary Central Nervous System Lymphoma.
Dörr JR, Thorwarth A, Mizia-Malarz A, Radke J, Tietze A, Hernáiz-Driever P, Horn D, Gratopp A, Eggert A, Deubzer HE.
Dörr JR, et al. Among authors: thorwarth a.
Children (Basel). 2021 Jun 2;8(6):469. doi: 10.3390/children8060469.
Children (Basel). 2021.
PMID: 34199532
Free PMC article.
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Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
Thorwarth A, Schnittert-Hübener S, Schrumpf P, Müller I, Jyrch S, Dame C, Biebermann H, Kleinau G, Katchanov J, Schuelke M, Ebert G, Steininger A, Bönnemann C, Brockmann K, Christen HJ, Crock P, deZegher F, Griese M, Hewitt J, Ivarsson S, Hübner C, Kapelari K, Plecko B, Rating D, Stoeva I, Ropers HH, Grüters A, Ullmann R, Krude H.
Thorwarth A, et al.
J Med Genet. 2014 Jun;51(6):375-87. doi: 10.1136/jmedgenet-2013-102248. Epub 2014 Apr 8.
J Med Genet. 2014.
PMID: 24714694
Free PMC article.
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Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular course.
Kallinich T, Thorwarth A, von Stuckrad SL, Rösen-Wolff A, Luksch H, Hundsdoerfer P, Minden K, Krawitz P.
Kallinich T, et al. Among authors: thorwarth a.
Pediatr Rheumatol Online J. 2016 Nov 24;14(1):63. doi: 10.1186/s12969-016-0124-2.
Pediatr Rheumatol Online J. 2016.
PMID: 27881174
Free PMC article.
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