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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 2
2003 5
2004 2
2005 1
2006 1
2007 3
2008 2
2009 4
2010 4
2011 5
2012 1
2013 5
2014 1
2015 2
2016 3
2017 3
2018 1
2024 0

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41 results

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Page 1
Infantile Frey's syndrome.
Tillman BN, Lesperance MM, Brinkmeier JV. Tillman BN, et al. Among authors: lesperance mm. Int J Pediatr Otorhinolaryngol. 2015 Jun;79(6):929-931. doi: 10.1016/j.ijporl.2015.03.023. Epub 2015 Apr 1. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25908408 Free PMC article. Review.
When do ranulas require a cervical approach?
Lesperance MM. Lesperance MM. Laryngoscope. 2013 Aug;123(8):1826-7. doi: 10.1002/lary.23937. Epub 2013 Feb 20. Laryngoscope. 2013. PMID: 23427070 Free article. Review. No abstract available.
Superior Canal Dehiscence Syndrome Affecting 3 Families.
Heidenreich KD, Kileny PR, Ahmed S, El-Kashlan HK, Melendez TL, Basura GJ, Lesperance MM. Heidenreich KD, et al. Among authors: lesperance mm. JAMA Otolaryngol Head Neck Surg. 2017 Jul 1;143(7):656-662. doi: 10.1001/jamaoto.2016.4743. JAMA Otolaryngol Head Neck Surg. 2017. PMID: 28384775 Free PMC article.
Temporal Bone Histopathology in NOG-Symphalangism Spectrum Disorder.
Quesnel AM, Nadol JB Jr, Nielsen GP, Curtin HD, Lesperance MM. Quesnel AM, et al. Among authors: lesperance mm. Otol Neurotol. 2015 Dec;36(10):1651-6. doi: 10.1097/MAO.0000000000000861. Otol Neurotol. 2015. PMID: 26474326 Free PMC article.
Clinical characterization of novel chromosome 22q13 microdeletions.
Ha JF, Ahmad A, Lesperance MM. Ha JF, et al. Among authors: lesperance mm. Int J Pediatr Otorhinolaryngol. 2017 Apr;95:121-126. doi: 10.1016/j.ijporl.2016.12.008. Epub 2016 Dec 23. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28576520
Proboscis lateralis: case report and review.
Thorne MC, Ruiz RE, Carvalho J, Lesperance MM. Thorne MC, et al. Among authors: lesperance mm. Arch Otolaryngol Head Neck Surg. 2007 Oct;133(10):1051-3. doi: 10.1001/archotol.133.10.1051. Arch Otolaryngol Head Neck Surg. 2007. PMID: 17938331 No abstract available.
Congenital cataracts in two siblings with Wolfram syndrome.
Mets RB, Emery SB, Lesperance MM, Mets MB. Mets RB, et al. Among authors: lesperance mm. Ophthalmic Genet. 2010 Dec;31(4):227-9. doi: 10.3109/13816810.2010.516056. Ophthalmic Genet. 2010. PMID: 21067485
41 results