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

Year Number of Results
2004 2
2006 2
2007 2
2008 1
2009 2
2010 1
2011 5
2012 6
2013 14
2014 13
2015 8
2016 6
2017 5
2018 7
2019 3
2020 4
2021 3
2022 3
2024 1

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76 results

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Page 1
Sleep Disorders in Adolescents.
Kansagra S. Kansagra S. Pediatrics. 2020 May;145(Suppl 2):S204-S209. doi: 10.1542/peds.2019-2056I. Pediatrics. 2020. PMID: 32358212 Review.
IRF2BPL Is Associated with Neurological Phenotypes.
Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Graham JM Jr, Ortiz D, Infante E, Steyaert W, Dermaut B, Poppe B, Chung HL, Zuo Z, Lee PT, Kanca O, Xia F, Yang Y, Smith EC, Jasien J, Kansagra S, Spiridigliozzi G, El-Dairi M, Lark R, Riley K, Koeberl DD, Golden-Grant K; Program for Undiagnosed Diseases (UD-PrOZA); Undiagnosed Diseases Network; Yamamoto S, Wangler MF, Mirzaa G, Hemelsoet D, Lee B, Nelson SF, Goldstein DB, Bellen HJ, Pena LDM. Marcogliese PC, et al. Among authors: kansagra s. Am J Hum Genet. 2018 Aug 2;103(2):245-260. doi: 10.1016/j.ajhg.2018.07.006. Epub 2018 Jul 26. Am J Hum Genet. 2018. PMID: 30057031 Free PMC article.
Alternating hemiplegia of childhood.
Kansagra S, Mikati MA, Vigevano F. Kansagra S, et al. Handb Clin Neurol. 2013;112:821-6. doi: 10.1016/B978-0-444-52910-7.00001-5. Handb Clin Neurol. 2013. PMID: 23622289 Review.
IRF2BPL Is Associated with Neurological Phenotypes.
Marcogliese PC, Shashi V, Spillmann RC, Stong N, Rosenfeld JA, Koenig MK, Martínez-Agosto JA, Herzog M, Chen AH, Dickson PI, Lin HJ, Vera MU, Salamon N, Graham JM Jr, Ortiz D, Infante E, Steyaert W, Dermaut B, Poppe B, Chung HL, Zuo Z, Lee PT, Kanca O, Xia F, Yang Y, Smith EC, Jasien J, Kansagra S, Spiridigliozzi G, El-Dairi M, Lark R, Riley K, Koeberl DD, Golden-Grant K; Program for Undiagnosed Diseases (UD-PrOZA); Undiagnosed Diseases Network; Yamamoto S, Wangler MF, Mirzaa G, Hemelsoet D, Lee B, Nelson SF, Goldstein DB, Bellen HJ, Pena LDM. Marcogliese PC, et al. Among authors: kansagra s. Am J Hum Genet. 2018 Sep 6;103(3):456. doi: 10.1016/j.ajhg.2018.08.010. Am J Hum Genet. 2018. PMID: 30193138 Free PMC article. No abstract available.
Epilepsy in neurofibromatosis type 1.
Pecoraro A, Arehart E, Gallentine W, Radtke R, Smith E, Pizoli C, Kansagra S, Abdelnour E, McLendon R, Mikati MA. Pecoraro A, et al. Among authors: kansagra s. Epilepsy Behav. 2017 Aug;73:137-141. doi: 10.1016/j.yebeh.2017.05.011. Epub 2017 Jul 18. Epilepsy Behav. 2017. PMID: 28633092
Epilepsy in KCNH1-related syndromes.
Mastrangelo M, Scheffer IE, Bramswig NC, Nair LD, Myers CT, Dentici ML, Korenke GC, Schoch K, Campeau PM, White SM, Shashi V, Kansagra S, Van Essen AJ, Leuzzi V. Mastrangelo M, et al. Among authors: kansagra s. Epileptic Disord. 2016 Jun 1;18(2):123-36. doi: 10.1684/epd.2016.0830. Epileptic Disord. 2016. PMID: 27267311
Polysomnographic findings in infantile Pompe disease.
Kansagra S, Austin S, DeArmey S, Kishnani PS, Kravitz RM. Kansagra S, et al. Am J Med Genet A. 2013 Dec;161A(12):3196-200. doi: 10.1002/ajmg.a.36227. Epub 2013 Oct 2. Am J Med Genet A. 2013. PMID: 24123966
76 results