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Year Number of Results
1985 1
1986 1
1987 1
1990 2
1991 3
1992 5
1993 4
1994 1
1995 1
1996 4
1997 1
1998 1
2000 1
2001 1
2002 3
2003 2
2004 4
2005 4
2006 3
2008 2
2009 3
2010 1
2012 2
2014 1
2015 2
2016 1
2019 2
2020 1
2021 2
2022 5
2023 2
2024 0

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66 results

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Page 1
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Among authors: hoogendijk je. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
Rhabdomyolysis after COVID-19 Comirnaty Vaccination: A Case Report.
Ruijters VJ, van der Meulen MFG, van Es MA, Smit T, Hoogendijk JE. Ruijters VJ, et al. Among authors: hoogendijk je. Case Rep Neurol. 2022 Nov 4;14(3):429-432. doi: 10.1159/000527599. eCollection 2022 Sep-Dec. Case Rep Neurol. 2022. PMID: 36636276 Free PMC article.
SMDT1 variants impair EMRE-mediated mitochondrial calcium uptake in patients with muscle involvement.
Bulthuis EP, Adjobo-Hermans MJW, de Potter B, Hoogstraten S, Wezendonk LHT, Tutakhel OAZ, Wintjes LT, van den Heuvel B, Willems PHGM, Kamsteeg EJ, Gozalbo MER, Sallevelt SCEH, Koudijs SM, Nicolai J, de Bie CI, Hoogendijk JE, Koopman WJH, Rodenburg RJ. Bulthuis EP, et al. Among authors: hoogendijk je. Biochim Biophys Acta Mol Basis Dis. 2023 Dec;1869(8):166808. doi: 10.1016/j.bbadis.2023.166808. Epub 2023 Jul 16. Biochim Biophys Acta Mol Basis Dis. 2023. PMID: 37454773 Free article.
Biomarker profiles of endothelial activation and dysfunction in rare systemic autoimmune diseases: implications for cardiovascular risk.
Wienke J, Mertens JS, Garcia S, Lim J, Wijngaarde CA, Yeo JG, Meyer A, van den Hoogen LL, Tekstra J, Hoogendijk JE, Otten HG, Fritsch-Stork RDE, de Jager W, Seyger MMB, Thurlings RM, de Jong EMGJ, van der Kooi AJ, van der Pol WL; Dutch Juvenile Myositis Consortium; Arkachaisri T, Radstake TRDJ, van Royen-Kerkhof A, van Wijk F. Wienke J, et al. Among authors: hoogendijk je. Rheumatology (Oxford). 2021 Feb 1;60(2):785-801. doi: 10.1093/rheumatology/keaa270. Rheumatology (Oxford). 2021. PMID: 32810267
Distal spinal muscular atrophy featured by predominant calf muscle involvement in VRK1 associated disease - Case series and review.
Demaegd K, Brilstra EH, Hoogendijk JE, de Bie CI, de Pagter MS, van Hecke W, Mühlebner A, van Es MA, Milone M, van Rheenen W. Demaegd K, et al. Among authors: hoogendijk je. Neuromuscul Disord. 2022 Jun;32(6):527-532. doi: 10.1016/j.nmd.2022.04.007. Epub 2022 Apr 27. Neuromuscul Disord. 2022. PMID: 35641352 Free article. Review.
Polymyositis: an overdiagnosed entity.
van der Meulen MF, Bronner IM, Hoogendijk JE, Burger H, van Venrooij WJ, Voskuyl AE, Dinant HJ, Linssen WH, Wokke JH, de Visser M. van der Meulen MF, et al. Among authors: hoogendijk je. Neurology. 2003 Aug 12;61(3):316-21. doi: 10.1212/wnl.61.3.316. Neurology. 2003. PMID: 12913190
Pathogenic variants in three families with distal muscle involvement.
Weterman MAJ, Bronk M, Jongejan A, Hoogendijk JE, Krudde J, Karjosukarso D, Goebel HH, Aronica E, Jöbsis GJ, van Ruissen F, van Spaendonck-Zwarts KY, de Visser M, Baas F. Weterman MAJ, et al. Among authors: hoogendijk je. Neuromuscul Disord. 2023 Jan;33(1):58-64. doi: 10.1016/j.nmd.2022.11.007. Epub 2022 Nov 29. Neuromuscul Disord. 2023. PMID: 36539320 Free article.
66 results