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Page 1
Intracranial calcifications in childhood: Part 2.
Gonçalves FG, Caschera L, Teixeira SR, Viaene AN, Pinelli L, Mankad K, Alves CAPF, Ortiz-Gonzalez XR, Andronikou S, Vossough A. Gonçalves FG, et al. Pediatr Radiol. 2020 Sep;50(10):1448-1475. doi: 10.1007/s00247-020-04716-y. Epub 2020 Jul 8. Pediatr Radiol. 2020. PMID: 32642802 Review.
Intracranial calcifications in childhood: Part 1.
Gonçalves FG, Caschera L, Teixeira SR, Viaene AN, Pinelli L, Mankad K, Alves CAPF, Ortiz-Gonzalez XR, Andronikou S, Vossough A. Gonçalves FG, et al. Pediatr Radiol. 2020 Sep;50(10):1424-1447. doi: 10.1007/s00247-020-04721-1. Epub 2020 Jul 30. Pediatr Radiol. 2020. PMID: 32734340 Review.
Focal cortical dysplasia is more common in boys than in girls.
Ortiz-González XR, Poduri A, Roberts CM, Sullivan JE, Marsh ED, Porter BE. Ortiz-González XR, et al. Epilepsy Behav. 2013 Apr;27(1):121-3. doi: 10.1016/j.yebeh.2012.12.035. Epub 2013 Feb 13. Epilepsy Behav. 2013. PMID: 23416281 Free PMC article.
Obituary: Jessica Anne Panzer, MD, PhD.
Ortiz-Gonzalez X, Goldberg EM, Banwell B. Ortiz-Gonzalez X, et al. Pediatr Neurol. 2017 Oct;75:4-5. doi: 10.1016/j.pediatrneurol.2017.07.007. Epub 2017 Jul 14. Pediatr Neurol. 2017. PMID: 28823630 No abstract available.
ANKRD11 variants: KBG syndrome and beyond.
Parenti I, Mallozzi MB, Hüning I, Gervasini C, Kuechler A, Agolini E, Albrecht B, Baquero-Montoya C, Bohring A, Bramswig NC, Busche A, Dalski A, Guo Y, Hanker B, Hellenbroich Y, Horn D, Innes AM, Leoni C, Li YR, Lynch SA, Mariani M, Medne L, Mikat B, Milani D, Onesimo R, Ortiz-Gonzalez X, Prott EC, Reutter H, Rossier E, Selicorni A, Wieacker P, Wilkens A, Wieczorek D, Zackai EH, Zampino G, Zirn B, Hakonarson H, Deardorff MA, Gillessen-Kaesbach G, Kaiser FJ. Parenti I, et al. Clin Genet. 2021 Aug;100(2):187-200. doi: 10.1111/cge.13977. Epub 2021 May 14. Clin Genet. 2021. PMID: 33955014 Free article.
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes.
Gustafson MA, McCormick EM, Perera L, Longley MJ, Bai R, Kong J, Dulik M, Shen L, Goldstein AC, McCormack SE, Laskin BL, Leroy BP, Ortiz-Gonzalez XR, Ellington MG, Copeland WC, Falk MJ. Gustafson MA, et al. PLoS One. 2019 Sep 3;14(9):e0221829. doi: 10.1371/journal.pone.0221829. eCollection 2019. PLoS One. 2019. PMID: 31479473 Free PMC article.
Ganglioglioma arising from dysplastic cortex.
Ortiz-González XR, Venneti S, Biegel JA, Rorke-Adams LB, Porter BE. Ortiz-González XR, et al. Epilepsia. 2011 Sep;52(9):e106-8. doi: 10.1111/j.1528-1167.2011.03124.x. Epub 2011 Jun 10. Epilepsia. 2011. PMID: 21668439 Free article.
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Li D, Yuan H, Ortiz-Gonzalez XR, Marsh ED, Tian L, McCormick EM, Kosobucki GJ, Chen W, Schulien AJ, Chiavacci R, Tankovic A, Naase C, Brueckner F, von Stülpnagel-Steinbeis C, Hu C, Kusumoto H, Hedrich UB, Elsen G, Hörtnagel K, Aizenman E, Lemke JR, Hakonarson H, Traynelis SF, Falk MJ. Li D, et al. Am J Hum Genet. 2016 Oct 6;99(4):802-816. doi: 10.1016/j.ajhg.2016.07.013. Epub 2016 Sep 8. Am J Hum Genet. 2016. PMID: 27616483 Free PMC article.
Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
Straub J, Konrad EDH, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, Dubbs H, Douglas G, Jobling R, Johnson D, Krock B, Mikati MA, Nesbitt A, Nicolai J, Phillips M, Poduri A, Ortiz-Gonzalez XR, Powis Z, Santani A, Smith L, Stegmann APA, Stumpel C, Vreeburg M; Deciphering Developmental Disorders Study; Fliedner A, Gregor A, Sticht H, Zweier C. Straub J, et al. Am J Hum Genet. 2018 Jan 4;102(1):44-57. doi: 10.1016/j.ajhg.2017.11.008. Epub 2017 Dec 21. Am J Hum Genet. 2018. PMID: 29276004 Free PMC article.
48 results