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Page 1
Pharmacogenetics of inflammatory bowel disease.
van den Bosch BJ, Coenen MJ. van den Bosch BJ, et al. Pharmacogenomics. 2021 Jan;22(1):55-66. doi: 10.2217/pgs-2020-0095. Epub 2020 Dec 11. Pharmacogenomics. 2021. PMID: 33305616 Review.
Potential added value of combined DPYD/DPD genotyping and phenotyping to prevent severe toxicity in patients with a DPYD variant and decreased dihydropyrimidine dehydrogenase enzyme activity.
Ockeloen CW, Raaijmakers A, Hijmans-van der Vegt M, Bierau J, de Vos-Geelen J, Willemsen AE, van den Bosch BJ, Coenen MJ. Ockeloen CW, et al. Among authors: van den bosch bj. J Oncol Pharm Pract. 2023 Jan;29(1):5-13. doi: 10.1177/10781552211049144. Epub 2021 Nov 19. J Oncol Pharm Pract. 2023. PMID: 34797200 Free PMC article.
Erythrocyte Inosine triphosphatase activity: A potential biomarker for adverse events during combination antiretroviral therapy for HIV.
Peltenburg NC, Bierau J, Bakker JA, Schippers JA, Lowe SH, Paulussen ADC, van den Bosch BJC, Leers MPG, Hansen BE, Verbon A. Peltenburg NC, et al. Among authors: van den bosch bjc. PLoS One. 2018 Jan 12;13(1):e0191069. doi: 10.1371/journal.pone.0191069. eCollection 2018. PLoS One. 2018. PMID: 29329318 Free PMC article.
The unfolding clinical spectrum of POLG mutations.
Blok MJ, van den Bosch BJ, Jongen E, Hendrickx A, de Die-Smulders CE, Hoogendijk JE, Brusse E, de Visser M, Poll-The BT, Bierau J, de Coo IF, Smeets HJ. Blok MJ, et al. Among authors: van den bosch bj. J Med Genet. 2009 Nov;46(11):776-85. doi: 10.1136/jmg.2009.067686. Epub 2009 Jul 2. J Med Genet. 2009. PMID: 19578034
Defective NDUFA9 as a novel cause of neonatally fatal complex I disease.
van den Bosch BJ, Gerards M, Sluiter W, Stegmann AP, Jongen EL, Hellebrekers DM, Oegema R, Lambrichs EH, Prokisch H, Danhauser K, Schoonderwoerd K, de Coo IF, Smeets HJ. van den Bosch BJ, et al. J Med Genet. 2012 Jan;49(1):10-5. doi: 10.1136/jmedgenet-2011-100466. Epub 2011 Nov 23. J Med Genet. 2012. PMID: 22114105
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.
Kamps R, Szklarczyk R, Theunissen TE, Hellebrekers DMEI, Sallevelt SCEH, Boesten IB, de Koning B, van den Bosch BJ, Salomons GS, Simas-Mendes M, Verdijk R, Schoonderwoerd K, de Coo IFM, Vanoevelen JM, Smeets HJM. Kamps R, et al. Among authors: van den bosch bj. Eur J Hum Genet. 2018 Apr;26(4):537-551. doi: 10.1038/s41431-017-0058-2. Epub 2018 Feb 13. Eur J Hum Genet. 2018. PMID: 29440775 Free PMC article.
31 results