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International Journal of Pediatric Otorhinolaryngology|May 10, 2017
Cochlear implantation and clinical features in patients with Noonan syndrome and Noonan syndrome with multiple lentigines caused by a mutation in PTPN11Josephine W I van Nierop, Dorothée C van Trier, Ineke van der Burgt, et al.
American Journal of Human Genetics|March 31, 2015
Mutations in DVL1 cause an osteosclerotic form of Robinow syndromeKieran J Bunn, Phil Daniel, Heleen S Rösken, et al.
Clinical Biochemistry|July 6, 2025
Concentration dependent impact of hemolysis on lipase result: Does it clinically matter?Janet R Zhou, Andrea Kunst, Joshua E Raizman, et al.
Molecular Genetics and Genomics : MGG|April 11, 2019
Insufficient evidence for a role of SERPINF1 in otosclerosisHanne Valgaeren, Manou Sommen, Matthias Beyens, et al.
Journal of Geriatric Oncology|August 9, 2021
Use of potentially inappropriate medication in older patients with lung cancer at the end of lifeLaurien Ham, Eric C T Geijteman, Mieke J Aarts, et al.
Trials|March 29, 2022
Effect of high-flow nasal therapy on patient-centred outcomes in patients at high risk of postoperative pulmonary complications after cardiac surgery: a study protocol for a multicentre adaptive randomised controlled trialMelissa Earwaker, Sofia Villar, Julia Fox-Rushby, et al.
American Journal of Human Genetics|March 30, 2010
Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunctionMargit Schraders, Jaap Oostrik, Patrick L M Huygen, et al.
Hearing Research|August 4, 2011
Audiometric characteristics of a Dutch family with Muckle-Wells syndromeN J D Weegerink, M Schraders, J Leijendeckers, et al.
Ear and Hearing|July 31, 2015
Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related DiseaseEva J J Verver, Vedat Topsakal, Henricus P M Kunst, et al.
Plos One|June 8, 2011
Bioassays to monitor Taspase1 function for the identification of pharmacogenetic inhibitorsShirley K Knauer, Verena Fetz, Jens Rabenstein, et al.
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