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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 1
1996 1
1997 1
1998 1
1999 3
2000 4
2001 3
2002 2
2003 6
2004 7
2005 10
2006 13
2007 7
2008 13
2009 5
2010 7
2011 13
2012 10
2013 8
2014 16
2015 9
2016 8
2017 8
2018 3
2019 2
2020 8
2021 4
2023 0
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Search Results

153 results
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Page 1
Delineation of target expression profiles in CD34+/CD38- and CD34+/CD38+ stem and progenitor cells in AML and CML.
Herrmann H, Sadovnik I, Eisenwort G, Rülicke T, Blatt K, Herndlhofer S, Willmann M, Stefanzl G, Baumgartner S, Greiner G, Schulenburg A, Mueller N, Rabitsch W, Bilban M, Hoermann G, Streubel B, Vallera DA, Sperr WR, Valent P. Herrmann H, et al. Among authors: streubel b. Blood Adv. 2020 Oct 27;4(20):5118-5132. doi: 10.1182/bloodadvances.2020001742. Blood Adv. 2020. PMID: 33085758 Free PMC article.
Molecular pathology of cancer: how to communicate with disease.
Birner P, Prager G, Streubel B. Birner P, et al. Among authors: streubel b. ESMO Open. 2016 Nov 17;1(5):e000085. doi: 10.1136/esmoopen-2016-000085. eCollection 2016. ESMO Open. 2016. PMID: 27933213 Free PMC article. Review.
Standards and impact of hematopathology in myelodysplastic syndromes (MDS).
Valent P, Orazi A, Büsche G, Schmitt-Gräff A, George TI, Sotlar K, Streubel B, Beham-Schmid C, Cerny-Reiterer S, Krieger O, van de Loosdrecht A, Kern W, Ogata K, Wimazal F, Várkonyi J, Sperr WR, Werner M, Kreipe H, Horny HP. Valent P, et al. Among authors: streubel b. Oncotarget. 2010 Nov;1(7):483-96. doi: 10.18632/oncotarget.101104. Oncotarget. 2010. PMID: 21317447 Free PMC article. Review.
Diagnostic strategy for females suspected of Fabry disease.
Balendran S, Oliva P, Sansen S, Mechtler TP, Streubel B, Cobos PN, Lukacs Z, Kasper DC. Balendran S, et al. Among authors: streubel b. Clin Genet. 2020 Apr;97(4):655-660. doi: 10.1111/cge.13694. Epub 2020 Jan 7. Clin Genet. 2020. PMID: 31860127
Novel clinically relevant genes in GIST--response.
Birner P, Streubel B. Birner P, et al. Among authors: streubel b. Clin Cancer Res. 2014 Apr 1;20(7):2015. doi: 10.1158/1078-0432.CCR-14-0028. Epub 2014 Feb 5. Clin Cancer Res. 2014. PMID: 24501393 No abstract available.
Deep-intronic variants in CNGB3 cause achromatopsia by pseudoexon activation.
Weisschuh N, Sturm M, Baumann B, Audo I, Ayuso C, Bocquet B, Branham K, Brooks BP, Catalá-Mora J, Giorda R, Heckenlively JR, Hufnagel RB, Jacobson SG, Kellner U, Kitsiou-Tzeli S, Matet A, Martorell Sampol L, Meunier I, Rudolph G, Sharon D, Stingl K, Streubel B, Varsányi B, Wissinger B, Kohl S. Weisschuh N, et al. Among authors: streubel b. Hum Mutat. 2020 Jan;41(1):255-264. doi: 10.1002/humu.23920. Epub 2019 Sep 30. Hum Mutat. 2020. PMID: 31544997 Free PMC article.
Prevalence of Fabry disease in men with tinnitus and sensorineural hearing loss.
Holy R, Hlozkova T, Prochazkova K, Kalfert D, Hybnerova F, Ebelova D, Streubel B, Chovanec M, Gal B, Linhart A, Astl J. Holy R, et al. Among authors: streubel b. J Appl Biomed. 2021 Mar;19(1):57-61. doi: 10.32725/jab.2021.003. Epub 2021 Jan 28. J Appl Biomed. 2021. PMID: 34907716 Free article.
Prenatal genetic counseling and consanguinity.
Posch A, Springer S, Langer M, Blaicher W, Streubel B, Schmid M. Posch A, et al. Among authors: streubel b. Prenat Diagn. 2012 Dec;32(12):1133-8. doi: 10.1002/pd.3971. Epub 2012 Sep 16. Prenat Diagn. 2012. PMID: 22987223
153 results