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Year Number of Results
1993 1
2007 1
2009 1
2010 4
2011 7
2012 7
2013 5
2014 3
2015 8
2016 7
2017 8
2018 3
2019 8
2020 9
2021 5
2022 2
2023 3
2024 2

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69 results

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Page 1
Physiological cell bioprinting density in human bone-derived cell-laden scaffolds enhances matrix mineralization rate and stiffness under dynamic loading.
de Leeuw AM, Graf R, Lim PJ, Zhang J, Schädli GN, Peterhans S, Rohrbach M, Giunta C, Rüger M, Rubert M, Müller R. de Leeuw AM, et al. Among authors: rohrbach m. Front Bioeng Biotechnol. 2024 Feb 14;12:1310289. doi: 10.3389/fbioe.2024.1310289. eCollection 2024. Front Bioeng Biotechnol. 2024. PMID: 38419730 Free PMC article.
Caregiver burden, and parents' perception of disease severity determine health-related quality of life in paediatric patients with intoxication-type inborn errors of metabolism.
Bösch F, Landolt MA, Baumgartner MR, Fernandez S, Forny P, Gautschi M, Grünert SC, Häberle J, Horvath C, Karall D, Lampis D, Rohrbach M, Scholl-Bürgi S, Szinnai G, Huemer M. Bösch F, et al. Among authors: rohrbach m. Mol Genet Metab Rep. 2022 May 6;31:100876. doi: 10.1016/j.ymgmr.2022.100876. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35762020 Free PMC article.
Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement.
Micale L, Morlino S, Carbone A, Carissimo A, Nardella G, Fusco C, Palumbo O, Schirizzi A, Russo F, Mazzoccoli G, Breckpot J, De Luca C, Ferraris A, Giunta C, Grammatico P, Haanpää MK, Mancano G, Forzano G, Cacchiarelli D, Van Esch H, Callewaert B, Rohrbach M, Castori M. Micale L, et al. Among authors: rohrbach m. Genet Med. 2022 Feb;24(2):439-453. doi: 10.1016/j.gim.2021.10.009. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906501 Free article.
Etiology of Carpal Tunnel Syndrome in a Large Cohort of Children.
Rüsch CT, Knirsch U, Weber DM, Rohrbach M, Eichenberger A, Lütschg J, Weber K, Broser PJ, Stettner GM. Rüsch CT, et al. Among authors: rohrbach m. Children (Basel). 2021 Jul 23;8(8):624. doi: 10.3390/children8080624. Children (Basel). 2021. PMID: 34438514 Free PMC article.
Omics Profiling of S2P Mutant Fibroblasts as a Mean to Unravel the Pathomechanism and Molecular Signatures of X-Linked MBTPS2 Osteogenesis Imperfecta.
Lim PJ, Marfurt S, Lindert U, Opitz L, Ndarugendamwo T, Srikanthan P, Poms M, Hersberger M, Langhans CD, Haas D, Rohrbach M, Giunta C. Lim PJ, et al. Among authors: rohrbach m. Front Genet. 2021 May 21;12:662751. doi: 10.3389/fgene.2021.662751. eCollection 2021. Front Genet. 2021. PMID: 34093655 Free PMC article.
69 results