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Page 1
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility.
Domené S, Stanescu H, Wallis D, Tinloy B, Pineda DE, Kleta R, Arcos-Burgos M, Roessler E, Muenke M. Domené S, et al. Among authors: tinloy b. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):11-8. doi: 10.1002/ajmg.b.31141. Epub 2010 Nov 12. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184580
Genetic basis of cystinosis in Turkish patients: a single-center experience.
Topaloglu R, Vilboux T, Coskun T, Ozaltin F, Tinloy B, Gunay-Aygun M, Bakkaloglu A, Besbas N, van den Heuvel L, Kleta R, Gahl WA. Topaloglu R, et al. Among authors: tinloy b. Pediatr Nephrol. 2012 Jan;27(1):115-21. doi: 10.1007/s00467-011-1942-6. Epub 2011 Jul 24. Pediatr Nephrol. 2012. PMID: 21786142 Free PMC article.
Cellular defects in Chediak-Higashi syndrome correlate with the molecular genotype and clinical phenotype.
Westbroek W, Adams D, Huizing M, Koshoffer A, Dorward H, Tinloy B, Parkes J, Helip-Wooley A, Kleta R, Tsilou E, Duvernay P, Digre KB, Creel DJ, White JG, Boissy RE, Gahl WA. Westbroek W, et al. Among authors: tinloy b. J Invest Dermatol. 2007 Nov;127(11):2674-7. doi: 10.1038/sj.jid.5700899. Epub 2007 May 31. J Invest Dermatol. 2007. PMID: 17554367 Free article. No abstract available.
Opening of Psychiatric Observation Unit Eases Boarding Crisis.
Parwani V, Tinloy B, Ulrich A, D'Onofrio G, Goldenberg M, Rothenberg C, Patel A, Venkatesh AK. Parwani V, et al. Among authors: tinloy b. Acad Emerg Med. 2018 Apr;25(4):456-460. doi: 10.1111/acem.13369. Epub 2018 Feb 1. Acad Emerg Med. 2018. PMID: 29266537 Free article.