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NPJ Cardiovascular Health|August 15, 2025
The senescence-inducing factor IGFBP7 and risk of atrial fibrillation: findings from the PREVEND studyNavin Suthahar, Ron T Gansevoort, Thomas F Kok, et al.
International Journal of Clinical Pharmacology and Therapeutics|February 28, 2007
Ibuprofen sodium dihydrate, an ibuprofen formulation with improved absorption characteristics, provides faster and greater pain relief than ibuprofen acidP Schleier, A Prochnau, A M Schmidt-Westhausen, et al.
Acta Obstetricia Et Gynecologica Scandinavica|April 20, 2020
Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature reviewOlav B Petersen, Eric Smith, Diane Van Opstal, et al.
American Journal of Medical Genetics. Part A|October 18, 2008
Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek populationHaris Kokotas, Lut Van Laer, Maria Grigoriadou, et al.
American Journal of Human Genetics|November 11, 1992
DNA polymorphism analysis in families with recurrence of free trisomy 21C G Pangalos, C C Talbot, J G Lewis, et al.
European Journal of Medical Genetics|February 21, 2012
Unexpected results in the constitution of small supernumerary marker chromosomesAnnalisa Vetro, Emmanouil Manolakos, Michael B Petersen, et al.
British Journal of Clinical Pharmacology|March 19, 2025
The tacrolimus concentration-to-dose ratio is associated with kidney function in heart transplant recipientsMaaike R Schagen, Teun B Petersen, Boris C A Seijkens, et al.
International Journal of Pediatric Otorhinolaryngology|November 9, 2010
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing lossHaris Kokotas, Maria Grigoriadou, Li Yang, et al.
Cytogenetic and Genome Research|May 23, 2015
35-Year Follow-Up of a Case of Ring Chromosome 2: Array-CGH Analysis and Literature Review of the Ring SyndromeCatherine Sarri, Sofia Douzgou, Haris Kontos, et al.
Molecular Genetics & Genomic Medicine|June 26, 2019
Partial trisomy 21 map: Ten cases further supporting the highly restricted Down syndrome critical region (HR-DSCR) on human chromosome 21Maria Chiara Pelleri, Elena Cicchini, Michael B Petersen, et al.
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