Author/Creator: de Laat, Paul - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator de Laat, Paul

1. Intra‐patient variability of heteroplasmy levels in urinary epithelial cells in carriers of the m.3243A>G mutation. Issue 2 (4th December 2018)

Authors:: de Laat, Paul; Rodenburg, Richard J.; Smeitink, Jan A. M.; Janssen, Mirian C. H.
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 7:Issue 2(2019)
Page Start:: n/a
Record Type:: Journal Article
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2. Quality of life, fatigue and mental health in patients with the m.3243A > G mutation and its correlates with genetic characteristics and disease manifestation. Issue 1 (December 2016)

Authors:: Verhaak, Christianne; de Laat, Paul; Koene, Saskia; Tibosch, Marijke; Rodenburg, Richard; Groot, Imelda; Knoop, Hans; Janssen, Mirian; Smeitink, Jan
Journal:: Orphanet journal of rare diseases
Issue:: Volume 11:Issue 1(2016)
Page Start:: 1
Record Type:: Journal Article
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3. Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variant. Issue 1 (21st May 2020)

Authors:: de Laat, Paul; Rodenburg, Richard R; Roeleveld, Nel; Koene, Saskia; Smeitink, Jan A; Janssen, Mirian CH
Journal:: Journal of medical genetics
Issue:: Volume 58:Issue 1(2021)
Page Start:: 48
Record Type:: Journal Article
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4. The KHENERGY Study: Safety and Efficacy of KH176 in Mitochondrial m.3243A>G Spectrum Disorders. Issue 1 (3rd September 2018)

Authors:: Janssen, Mirian C.H.; Koene, Saskia; de Laat, Paul; Hemelaar, Pleun; Pickkers, Peter; Spaans, Edwin; Beukema, Rypko; Beyrath, Julien; Groothuis, Jan; Verhaak, Chris; Smeitink, Jan
Journal:: Clinical pharmacology & therapeutics
Issue:: Volume 105:Issue 1(2019)
Page Start:: 101
Record Type:: Journal Article
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