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Acute and chronic neuroborreliosis with and without CNS involvement: a clinical, MRI, and HLA study of 27 cases.
Krüger H, Heim E, Schuknecht B, Scholz S. Krüger H, et al. Among authors: scholz s. J Neurol. 1991 Aug;238(5):271-80. doi: 10.1007/BF00319739. J Neurol. 1991. PMID: 1919611
Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical course.
Poller W, Faber JP, Scholz S, Olek K, Müller KM. Poller W, et al. Among authors: scholz s. Klin Wochenschr. 1991 Sep 16;69(14):657-63. doi: 10.1007/BF01649427. Klin Wochenschr. 1991. PMID: 1749205
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease.
Poller W, Faber JP, Weidinger S, Tief K, Scholz S, Fischer M, Olek K, Kirchgesser M, Heidtmann HH. Poller W, et al. Among authors: scholz s. Genomics. 1993 Sep;17(3):740-3. doi: 10.1006/geno.1993.1396. Genomics. 1993. PMID: 8244391
Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease.
Poller W, Faber JP, Scholz S, Weidinger S, Bartholomé K, Olek K, Eriksson S. Poller W, et al. Among authors: scholz s. Lancet. 1992 Jun 20;339(8808):1538. doi: 10.1016/0140-6736(92)91301-n. Lancet. 1992. PMID: 1351206 No abstract available.
Salt dependence, kinetic properties and catalytic mechanism of N-formylmethanofuran:tetrahydromethanopterin formyltransferase from the extreme thermophile Methanopyrus kandleri.
Breitung J, Börner G, Scholz S, Linder D, Stetter KO, Thauer RK. Breitung J, et al. Among authors: scholz s. Eur J Biochem. 1992 Dec 15;210(3):971-81. doi: 10.1111/j.1432-1033.1992.tb17502.x. Eur J Biochem. 1992. PMID: 1483480
Di-myo-inositol-1,1'-phosphate: a new inositol phosphate isolated from Pyrococcus woesei.
Scholz S, Sonnenbichler J, Schäfer W, Hensel R. Scholz S, et al. FEBS Lett. 1992 Jul 20;306(2-3):239-42. doi: 10.1016/0014-5793(92)81008-a. FEBS Lett. 1992. PMID: 1633880
SF3B1 and BAP1 mutations in blue nevus-like melanoma.
Griewank KG, Müller H, Jackett LA, Emberger M, Möller I, van de Nes JA, Zimmer L, Livingstone E, Wiesner T, Scholz SL, Cosgarea I, Sucker A, Schimming T, Hillen U, Schilling B, Paschen A, Reis H, Mentzel T, Kutzner H, Rütten A, Murali R, Scolyer RA, Schadendorf D. Griewank KG, et al. Mod Pathol. 2017 Jul;30(7):928-939. doi: 10.1038/modpathol.2017.23. Epub 2017 Apr 14. Mod Pathol. 2017. PMID: 28409567 Free PMC article.
Frequent GNAQ, GNA11, and EIF1AX Mutations in Iris Melanoma.
Scholz SL, Möller I, Reis H, Süßkind D, van de Nes JAP, Leonardelli S, Schilling B, Livingstone E, Schimming T, Paschen A, Sucker A, Murali R, Steuhl KP, Schadendorf D, Westekemper H, Griewank KG. Scholz SL, et al. Invest Ophthalmol Vis Sci. 2017 Jul 1;58(9):3464-3470. doi: 10.1167/iovs.17-21838. Invest Ophthalmol Vis Sci. 2017. PMID: 28700778
TERT promoter mutations in ocular melanoma distinguish between conjunctival and uveal tumours.
Griewank KG, Murali R, Schilling B, Scholz S, Sucker A, Song M, Süsskind D, Grabellus F, Zimmer L, Hillen U, Steuhl KP, Schadendorf D, Westekemper H, Zeschnigk M. Griewank KG, et al. Among authors: scholz s. Br J Cancer. 2013 Jul 23;109(2):497-501. doi: 10.1038/bjc.2013.312. Epub 2013 Jun 25. Br J Cancer. 2013. PMID: 23799844 Free PMC article.
Analysis of SDHD promoter mutations in various types of melanoma.
Scholz SL, Horn S, Murali R, Möller I, Sucker A, Sondermann W, Stiller M, Schilling B, Livingstone E, Zimmer L, Reis H, Metz CH, Zeschnigk M, Paschen A, Steuhl KP, Schadendorf D, Westekemper H, Griewank KG. Scholz SL, et al. Oncotarget. 2015 Sep 22;6(28):25868-82. doi: 10.18632/oncotarget.4665. Oncotarget. 2015. PMID: 26327518 Free PMC article.
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