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

Year Number of Results
1974 2
1975 2
1977 2
1979 3
1980 1
1981 1
1984 1
1985 2
1986 2
1987 4
1988 1
1989 4
1990 1
1991 4
1992 1
1993 2
1994 3
1995 2
1996 7
1997 4
1998 4
1999 3
2000 2
2001 5
2002 4
2003 10
2004 5
2005 6
2006 9
2007 17
2008 30
2009 24
2010 18
2011 20
2012 18
2013 30
2014 33
2015 22
2016 20
2017 24
2018 17
2019 17
2020 6
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Article attribute
Article type
Publication date

Search Results

351 results
Results by year
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Page 1
Hypophosphatasia: From Diagnosis to Treatment.
Simon S, Resch H, Klaushofer K, Roschger P, Zwerina J, Kocijan R. Simon S, et al. Among authors: Klaushofer K. Curr Rheumatol Rep. 2018 Sep 10;20(11):69. doi: 10.1007/s11926-018-0778-5. Curr Rheumatol Rep. 2018. PMID: 30203264 Review.
Somatic activating mutations in MAP2K1 cause melorheostosis.
Kang H, Jha S, Deng Z, Fratzl-Zelman N, Cabral WA, Ivovic A, Meylan F, Hanson EP, Lange E, Katz J, Roschger P, Klaushofer K, Cowen EW, Siegel RM, Marini JC, Bhattacharyya T. Kang H, et al. Among authors: Klaushofer K. Nat Commun. 2018 Apr 11;9(1):1390. doi: 10.1038/s41467-018-03720-z. Nat Commun. 2018. PMID: 29643386 Free PMC article.
Vitamin D and calcium supplementation for three years in postmenopausal osteoporosis significantly alters bone mineral and organic matrix quality.
Paschalis EP, Gamsjaeger S, Hassler N, Fahrleitner-Pammer A, Dobnig H, Stepan JJ, Pavo I, Eriksen EF, Klaushofer K. Paschalis EP, et al. Among authors: Klaushofer K. Bone. 2017 Feb;95:41-46. doi: 10.1016/j.bone.2016.11.002. Epub 2016 Nov 5. Bone. 2017. PMID: 27826025
Impaired osteocyte maturation in the pathogenesis of renal osteodystrophy.
Pereira RC, Salusky IB, Roschger P, Klaushofer K, Yadin O, Freymiller EG, Bowen R, Delany AM, Fratzl-Zelman N, Wesseling-Perry K. Pereira RC, et al. Among authors: Klaushofer K. Kidney Int. 2018 Nov;94(5):1002-1012. doi: 10.1016/j.kint.2018.08.011. Kidney Int. 2018. PMID: 30348285 Free PMC article.
HFE hemochromatosis screening in patients with severe hip osteoarthritis: A prospective cross-sectional study.
Oppl B, Husar-Memmer E, Pfefferkorn S, Blank M, Zenz P, Gollob E, Wurnig C, Engel A, Stadlmayr A, Uyanik G, Brozek W, Klaushofer K, Zwerina J, Datz C. Oppl B, et al. Among authors: Klaushofer K. PLoS One. 2018 Nov 14;13(11):e0207415. doi: 10.1371/journal.pone.0207415. eCollection 2018. PLoS One. 2018. PMID: 30427934 Free PMC article.
Biomechanical and Bone Material Properties of Schnurri-3 Null Mice.
Hofstaetter JG, Misof BM, Jones DC, Zoehrer R, Blouin S, Schueler C, Paschalis EP, Erben RG, Weinkamer R, Klaushofer K, Roschger P. Hofstaetter JG, et al. Among authors: Klaushofer K. JBMR Plus. 2019 Sep 11;3(11):e10226. doi: 10.1002/jbm4.10226. eCollection 2019 Nov. JBMR Plus. 2019. PMID: 31768487 Free PMC article.
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays.
Windpassinger C, Piard J, Bonnard C, Alfadhel M, Lim S, Bisteau X, Blouin S, Ali NB, Ng AYJ, Lu H, Tohari S, Talib SZA, van Hul N, Caldez MJ, Van Maldergem L, Yigit G, Kayserili H, Youssef SA, Coppola V, de Bruin A, Tessarollo L, Choi H, Rupp V, Roetzer K, Roschger P, Klaushofer K, Altmüller J, Roy S, Venkatesh B, Ganger R, Grill F, Ben Chehida F, Wollnik B, Altunoglu U, Al Kaissi A, Reversade B, Kaldis P. Windpassinger C, et al. Among authors: Klaushofer K. Am J Hum Genet. 2017 Sep 7;101(3):391-403. doi: 10.1016/j.ajhg.2017.08.003. Am J Hum Genet. 2017. PMID: 28886341 Free PMC article.
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular Defect.
Webb EA, Balasubramanian M, Fratzl-Zelman N, Cabral WA, Titheradge H, Alsaedi A, Saraff V, Vogt J, Cole T, Stewart S, Crabtree NJ, Sargent BM, Gamsjaeger S, Paschalis EP, Roschger P, Klaushofer K, Shaw NJ, Marini JC, Högler W. Webb EA, et al. Among authors: Klaushofer K. J Clin Endocrinol Metab. 2017 Jun 1;102(6):2019-2028. doi: 10.1210/jc.2016-3766. J Clin Endocrinol Metab. 2017. PMID: 28323974 Free PMC article.
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