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The molar tooth sign is pathognomonic for Joubert syndrome!
Poretti A, Boltshauser E, Valente EM. Poretti A, et al. Among authors: boltshauser e. Pediatr Neurol. 2014 Jun;50(6):e15-6. doi: 10.1016/j.pediatrneurol.2013.11.003. Epub 2013 Nov 14. Pediatr Neurol. 2014. PMID: 24731480 No abstract available.
Clinical utility gene card for: Joubert syndrome.
Valente EM, Brancati F, Boltshauser E, Dallapiccola B. Valente EM, et al. Among authors: boltshauser e. Eur J Hum Genet. 2011 Sep;19(9). doi: 10.1038/ejhg.2011.49. Epub 2011 Mar 30. Eur J Hum Genet. 2011. PMID: 21448235 Free PMC article. No abstract available.
Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders.
Travaglini L, Brancati F, Silhavy J, Iannicelli M, Nickerson E, Elkhartoufi N, Scott E, Spencer E, Gabriel S, Thomas S, Ben-Zeev B, Bertini E, Boltshauser E, Chaouch M, Cilio MR, de Jong MM, Kayserili H, Ogur G, Poretti A, Signorini S, Uziel G, Zaki MS; International JSRD Study Group; Johnson C, Attié-Bitach T, Gleeson JG, Valente EM. Travaglini L, et al. Among authors: boltshauser e. Eur J Hum Genet. 2013 Oct;21(10):1074-8. doi: 10.1038/ejhg.2012.305. Epub 2013 Feb 6. Eur J Hum Genet. 2013. PMID: 23386033 Free PMC article.
Clinical utility gene card for: Joubert syndrome--update 2013.
Valente EM, Brancati F, Boltshauser E, Dallapiccola B. Valente EM, et al. Among authors: boltshauser e. Eur J Hum Genet. 2013 Oct;21(10). doi: 10.1038/ejhg.2013.10. Epub 2013 Feb 13. Eur J Hum Genet. 2013. PMID: 23403901 Free PMC article. No abstract available.
Horizontal head titubation in infants with Joubert syndrome: a new finding.
Poretti A, Christen HJ, Elton LE, Baumgartner M, Korenke GC, Sukhudyan B, Hethey S, Cross E, Steinlin M, Boltshauser E. Poretti A, et al. Among authors: boltshauser e. Dev Med Child Neurol. 2014 Oct;56(10):1016-20. doi: 10.1111/dmcn.12489. Epub 2014 May 10. Dev Med Child Neurol. 2014. PMID: 24814865 Free article.
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes.
Roosing S, Romani M, Isrie M, Rosti RO, Micalizzi A, Musaev D, Mazza T, Al-Gazali L, Altunoglu U, Boltshauser E, D'Arrigo S, De Keersmaecker B, Kayserili H, Brandenberger S, Kraoua I, Mark PR, McKanna T, Van Keirsbilck J, Moerman P, Poretti A, Puri R, Van Esch H, Gleeson JG, Valente EM. Roosing S, et al. Among authors: boltshauser e. J Med Genet. 2016 Sep;53(9):608-15. doi: 10.1136/jmedgenet-2016-103832. Epub 2016 May 6. J Med Genet. 2016. PMID: 27208211 Free PMC article.
Differential diagnosis of cerebellar atrophy in childhood.
Poretti A, Wolf NI, Boltshauser E. Poretti A, et al. Among authors: boltshauser e. Eur J Paediatr Neurol. 2008 May;12(3):155-67. doi: 10.1016/j.ejpn.2007.07.010. Epub 2007 Sep 14. Eur J Paediatr Neurol. 2008. PMID: 17869142 Review.
Gomez-Lopez-Hernandez syndrome: an easily missed diagnosis.
Poretti A, Bartholdi D, Gobara S, Alber FD, Boltshauser E. Poretti A, et al. Among authors: boltshauser e. Eur J Med Genet. 2008 May-Jun;51(3):197-208. doi: 10.1016/j.ejmg.2008.01.004. Epub 2008 Feb 8. Eur J Med Genet. 2008. PMID: 18342593
416 results