Crino P - Search Results

1

Hemimegalencephaly: foetal tauopathy with mTOR hyperactivation and neuronal lipidosis.

Sarnat H, Flores-Sarnat L, Crino P, Hader W, Bello-Espinosa L. Sarnat H, et al. Among authors: crino p. Folia Neuropathol. 2012;50(4):330-45. doi: 10.5114/fn.2012.32363. Folia Neuropathol. 2012. PMID: 23319189 Free article.

2

Fetal brain lesions in tuberous sclerosis complex: TORC1 activation and inflammation.

Prabowo AS, Anink JJ, Lammens M, Nellist M, van den Ouweland AM, Adle-Biassette H, Sarnat HB, Flores-Sarnat L, Crino PB, Aronica E. Prabowo AS, et al. Brain Pathol. 2013 Jan;23(1):45-59. doi: 10.1111/j.1750-3639.2012.00616.x. Epub 2012 Aug 30. Brain Pathol. 2013. PMID: 22805177 Free PMC article.

3

Fetal brain mTOR signaling activation in tuberous sclerosis complex.

Tsai V, Parker WE, Orlova KA, Baybis M, Chi AW, Berg BD, Birnbaum JF, Estevez J, Okochi K, Sarnat HB, Flores-Sarnat L, Aronica E, Crino PB. Tsai V, et al. Cereb Cortex. 2014 Feb;24(2):315-27. doi: 10.1093/cercor/bhs310. Epub 2012 Oct 18. Cereb Cortex. 2014. PMID: 23081885 Free PMC article.

4

Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility.

Leventer RJ, Jansen FE, Mandelstam SA, Ho A, Mohamed I, Sarnat HB, Kato M, Fukasawa T, Saitsu H, Matsumoto N, Itoh M, Kalnins RM, Chow CW, Harvey AS, Jackson GD, Crino PB, Berkovic SF, Scheffer IE. Leventer RJ, et al. Epilepsia. 2014 Mar;55(3):e22-6. doi: 10.1111/epi.12533. Epub 2014 Feb 6. Epilepsia. 2014. PMID: 24502525 Free article.

5

Co-expression of cyclin D1 and phosphorylated ribosomal S6 proteins in hemimegalencephaly.

Aronica E, Boer K, Baybis M, Yu J, Crino P. Aronica E, et al. Among authors: crino p. Acta Neuropathol. 2007 Sep;114(3):287-93. doi: 10.1007/s00401-007-0225-6. Epub 2007 May 5. Acta Neuropathol. 2007. PMID: 17483958

6

Deletion of 15q11.2-15q13.1 in isolated human hemimegalencephaly.

Baybis M, Aronica E, Nathanson KL, Crino PB. Baybis M, et al. Acta Neuropathol. 2009 Dec;118(6):821-3. doi: 10.1007/s00401-009-0603-3. Epub 2009 Oct 23. Acta Neuropathol. 2009. PMID: 19851776 No abstract available.

7

Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR.

Leventer RJ, Scerri T, Marsh AP, Pope K, Gillies G, Maixner W, MacGregor D, Harvey AS, Delatycki MB, Amor DJ, Crino P, Bahlo M, Lockhart PJ. Leventer RJ, et al. Among authors: crino p. Neurology. 2015 May 19;84(20):2029-32. doi: 10.1212/WNL.0000000000001594. Epub 2015 Apr 15. Neurology. 2015. PMID: 25878179 Free PMC article.

8

GATORopathies: The role of amino acid regulatory gene mutations in epilepsy and cortical malformations.

Iffland PH 2nd, Carson V, Bordey A, Crino PB. Iffland PH 2nd, et al. Epilepsia. 2019 Nov;60(11):2163-2173. doi: 10.1111/epi.16370. Epub 2019 Oct 17. Epilepsia. 2019. PMID: 31625153 Free PMC article. Review.

9

mTOR signaling in epilepsy: insights from malformations of cortical development.

Crino PB. Crino PB. Cold Spring Harb Perspect Med. 2015 Apr 1;5(4):a022442. doi: 10.1101/cshperspect.a022442. Cold Spring Harb Perspect Med. 2015. PMID: 25833943 Free PMC article. Review.

10

Evolving neurobiology of tuberous sclerosis complex.

Crino PB. Crino PB. Acta Neuropathol. 2013 Mar;125(3):317-32. doi: 10.1007/s00401-013-1085-x. Epub 2013 Feb 6. Acta Neuropathol. 2013. PMID: 23386324 Review.

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