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

Year Number of Results
1989 4
1990 3
1991 1
1992 2
1993 2
1994 1
1995 2
1996 3
1997 4
1998 1
1999 3
2000 2
2001 6
2002 5
2003 6
2004 8
2005 6
2006 3
2007 9
2008 4
2009 4
2010 8
2011 4
2012 7
2013 5
2014 4
2015 9
2016 6
2017 4
2018 5
2019 3
2020 3
2021 4
2022 8
2023 7
2024 4
2025 0

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148 results

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Page 1
KPTN-Related Disorder.
Rawlins LE, Crino PB, Iffland PH, Crosby AH, Baple EL. Rawlins LE, et al. Among authors: crino pb. 2024 Aug 1. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2024 Aug 1. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 39083632 Free Books & Documents. Review.
Tuberous sclerosis complex.
Hasbani DM, Crino PB. Hasbani DM, et al. Among authors: crino pb. Handb Clin Neurol. 2018;148:813-822. doi: 10.1016/B978-0-444-64076-5.00052-1. Handb Clin Neurol. 2018. PMID: 29478616 Review.
Focal Cortical Dysplasia.
Crino PB. Crino PB. Semin Neurol. 2015 Jun;35(3):201-8. doi: 10.1055/s-0035-1552617. Epub 2015 Jun 10. Semin Neurol. 2015. PMID: 26060899 Free PMC article. Review.
Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes.
Levitin MO, Rawlins LE, Sanchez-Andrade G, Arshad OA, Collins SC, Sawiak SJ, Iffland PH 2nd, Andersson MHL, Bupp C, Cambridge EL, Coomber EL, Ellis I, Herkert JC, Ironfield H, Jory L, Kretz PF, Kant SG, Neaverson A, Nibbeling E, Rowley C, Relton E, Sanderson M, Scott EM, Stewart H, Shuen AY, Schreiber J, Tuck L, Tonks J, Terkelsen T, van Ravenswaaij-Arts C, Vasudevan P, Wenger O, Wright M, Day A, Hunter A, Patel M, Lelliott CJ, Crino PB, Yalcin B, Crosby AH, Baple EL, Logan DW, Hurles ME, Gerety SS. Levitin MO, et al. Among authors: crino pb. Brain. 2023 Nov 2;146(11):4766-4783. doi: 10.1093/brain/awad231. Brain. 2023. PMID: 37437211 Free PMC article.
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, Von Allmen GK, Rodziyevska O, Bhattacharjee MB, Lidov HGW, Vogel H, Grant GA, Porter BE, Poduri AH, Crino PB, Heinzen EL. Lai D, et al. Among authors: crino pb. Brain. 2022 Aug 27;145(8):2704-2720. doi: 10.1093/brain/awac117. Brain. 2022. PMID: 35441233 Free PMC article.
Loss of Slc35a2 alters development of the mouse cerebral cortex.
Elziny S, Sran S, Yoon H, Corrigan RR, Page J, Ringland A, Lanier A, Lapidus S, Foreman J, Heinzen EL, Iffland P, Crino PB, Bedrosian TA. Elziny S, et al. Among authors: crino pb. Neurosci Lett. 2024 Jul 27;836:137881. doi: 10.1016/j.neulet.2024.137881. Epub 2024 Jun 22. Neurosci Lett. 2024. PMID: 38909838 Free article.
mTORopathies: A Road Well-Traveled.
Crino PB. Crino PB. Epilepsy Curr. 2020 Nov-Dec;20(6_suppl):64S-66S. doi: 10.1177/1535759720959320. Epub 2020 Oct 14. Epilepsy Curr. 2020. PMID: 33052752 Free PMC article. No abstract available.
The tuberous sclerosis complex.
Orlova KA, Crino PB. Orlova KA, et al. Among authors: crino pb. Ann N Y Acad Sci. 2010 Jan;1184:87-105. doi: 10.1111/j.1749-6632.2009.05117.x. Ann N Y Acad Sci. 2010. PMID: 20146692 Free PMC article. Review.
The tuberous sclerosis complex.
Crino PB, Nathanson KL, Henske EP. Crino PB, et al. N Engl J Med. 2006 Sep 28;355(13):1345-56. doi: 10.1056/NEJMra055323. N Engl J Med. 2006. PMID: 17005952 Review. No abstract available.
148 results