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

Year Number of Results
1991 1
1992 1
1993 3
1994 5
1995 7
1997 7
1998 2
1999 5
2000 3
2002 4
2003 5
2004 7
2005 9
2006 3
2007 2
2008 5
2009 5
2010 5
2011 2
2012 9
2013 2
2014 3
2015 8
2016 6
2017 4
2018 8
2019 11
2020 15
2021 26
2022 15
2023 25
2024 10

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209 results

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Page 1
Current concepts in the pathogenesis and treatment of chronic suppurative otitis media.
Mittal R, Lisi CV, Gerring R, Mittal J, Mathee K, Narasimhan G, Azad RK, Yao Q, Grati M, Yan D, Eshraghi AA, Angeli SI, Telischi FF, Liu XZ. Mittal R, et al. Among authors: telischi ff. J Med Microbiol. 2015 Oct;64(10):1103-1116. doi: 10.1099/jmm.0.000155. Epub 2015 Aug 5. J Med Microbiol. 2015. PMID: 26248613 Free PMC article. Review.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations.
Rodan LH, Spillmann RC, Kurata HT, Lamothe SM, Maghera J, Jamra RA, Alkelai A, Antonarakis SE, Atallah I, Bar-Yosef O, Bilan F, Bjorgo K, Blanc X, Van Bogaert P, Bolkier Y, Burrage LC, Christ BU, Granadillo JL, Dickson P, Donald KA, Dubourg C, Eliyahu A, Emrick L, Engleman K, Gonfiantini MV, Good JM, Kalser J, Kloeckner C, Lachmeijer G, Macchiaiolo M, Nicita F, Odent S, O'Heir E, Ortiz-Gonzalez X, Pacio-Miguez M, Palomares-Bralo M, Pena L, Platzer K, Quinodoz M, Ranza E, Rosenfeld JA, Roulet-Perez E, Santani A, Santos-Simarro F, Pode-Shakked B, Skraban C, Slaugh R, Superti-Furga A, Thiffault I, van Jaabrsveld RH, Vincent M, Wang HG, Zacher P; Undiagnosed Diseases Network; Rush E, Pitt GS, Au PYB, Shashi V. Rodan LH, et al. Genet Med. 2021 Oct;23(10):1922-1932. doi: 10.1038/s41436-021-01232-8. Epub 2021 Jun 23. Genet Med. 2021. PMID: 34163037 Free PMC article.
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.
Remembering Dr. Giovana R. Thomas.
Telischi FF, Weed DT. Telischi FF, et al. Laryngoscope. 2023 Oct;133(10):2440-2442. doi: 10.1002/lary.30847. Epub 2023 Jul 12. Laryngoscope. 2023. PMID: 37435849 No abstract available.
Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Kozycki CT, Kodati S, Huryn L, Wang H, Warner BM, Jani P, Hammoud D, Abu-Asab MS, Jittayasothorn Y, Mattapallil MJ, Tsai WL, Ullah E, Zhou P, Tian X, Soldatos A, Moutsopoulos N, Kao-Hsieh M, Heller T, Cowen EW, Lee CR, Toro C, Kalsi S, Khavandgar Z, Baer A, Beach M, Long Priel D, Nehrebecky M, Rosenzweig S, Romeo T, Deuitch N, Brenchley L, Pelayo E, Zein W, Sen N, Yang AH, Farley G, Sweetser DA, Briere L, Yang J, de Oliveira Poswar F, Schwartz IVD, Silva Alves T, Dusser P, Koné-Paut I, Touitou I, Titah SM, van Hagen PM, van Wijck RTA, van der Spek PJ, Yano H, Benneche A, Apalset EM, Jansson RW, Caspi RR, Kuhns DB, Gadina M, Takada H, Ida H, Nishikomori R, Verrecchia E, Sangiorgi E, Manna R, Brooks BP, Sobrin L, Hufnagel RB, Beck D, Shao F, Ombrello AK, Aksentijevich I, Kastner DL; Undiagnosed Diseases Network. Kozycki CT, et al. Ann Rheum Dis. 2022 Oct;81(10):1453-1464. doi: 10.1136/annrheumdis-2022-222629. Epub 2022 Jul 22. Ann Rheum Dis. 2022. PMID: 35868845 Free PMC article.
Otosclerosis and Stapes Surgery.
Eshraghi AA, Telischi FF. Eshraghi AA, et al. Among authors: telischi ff. Otolaryngol Clin North Am. 2018 Apr;51(2):xvii-xix. doi: 10.1016/j.otc.2017.12.001. Otolaryngol Clin North Am. 2018. PMID: 29502732 No abstract available.
Tympanomeatal flaps.
Balkany TJ, Telischi FF, Angeli SI, Eshraghi AA. Balkany TJ, et al. Among authors: telischi ff. Laryngoscope. 2003 Jul;113(7):1266-8. doi: 10.1097/00005537-200307000-00028. Laryngoscope. 2003. PMID: 12838030 No abstract available.
Cochlear reimplantation.
Balkany TJ, Hodges AV, Gómez-Marín O, Bird PA, Dolan-Ash S, Butts S, Telischi FF, Lee D. Balkany TJ, et al. Among authors: telischi ff. Laryngoscope. 1999 Mar;109(3):351-5. doi: 10.1097/00005537-199903000-00002. Laryngoscope. 1999. PMID: 10089956
Advanced Otosclerosis: Stapes Surgery or Cochlear Implantation?
Eshraghi AA, Ila K, Ocak E, Telischi FF. Eshraghi AA, et al. Among authors: telischi ff. Otolaryngol Clin North Am. 2018 Apr;51(2):429-440. doi: 10.1016/j.otc.2017.11.012. Otolaryngol Clin North Am. 2018. PMID: 29502727 Review.
Macrocephaly and developmental delay caused by missense variants in RAB5C.
Koop K, Yuan W, Tessadori F, Rodriguez-Polanco WR, Grubbs J, Zhang B, Osmond M, Graham G, Sawyer S, Conboy E, Vetrini F, Treat K, Płoski R, Pienkowski VM, Kłosowska A, Fieg E, Krier J, Mallebranche C, Alban Z, Aldinger KA, Ritter D, Macnamara E, Sullivan B, Herriges J, Alaimo JT, Helbig C, Ellis CA, van Eyk C, Gecz J, Farrugia D, Osei-Owusu I, Adès L, van den Boogaard MJ, Fuchs S, Bakker J, Duran K, Dawson ZD, Lindsey A, Huang H, Baldridge D, Silverman GA, Grant BD, Raizen D; Undiagnosed Diseases Network; van Haaften G, Pak SC, Rehmann H, Schedl T, van Hasselt P. Koop K, et al. Hum Mol Genet. 2023 Oct 17;32(21):3063-3077. doi: 10.1093/hmg/ddad130. Hum Mol Genet. 2023. PMID: 37552066 Free PMC article.
209 results