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

Year Number of Results
2003 2
2004 1
2005 2
2011 1
2012 1
2013 1
2014 2
2015 7
2016 2
2017 6
2018 3
2019 1
2021 3
2023 2
2024 1

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30 results

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Page 1
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk.
Oliver KL, Trivisano M, Mandelstam SA, De Dominicis A, Francis DI, Green TE, Muir AM, Chowdhary A, Hertzberg C, Goldhahn K, Metreau J, Prager C, Pinner J, Cardamone M, Myers KA, Leventer RJ, Lesca G, Bahlo M, Hildebrand MS, Mefford HC, Kaindl AM, Specchio N, Scheffer IE. Oliver KL, et al. Among authors: mandelstam sa. Epilepsia. 2023 May;64(5):1351-1367. doi: 10.1111/epi.17542. Epub 2023 Mar 11. Epilepsia. 2023. PMID: 36779245 Free PMC article.
Aicardi Syndrome Is a Genetically Heterogeneous Disorder.
Ha TT, Burgess R, Newman M, Moey C, Mandelstam SA, Gardner AE, Ivancevic AM, Pham D, Kumar R, Smith N, Patel C, Malone S, Ryan MM, Calvert S, van Eyk CL, Lardelli M, Berkovic SF, Leventer RJ, Richards LJ, Scheffer IE, Gecz J, Corbett MA. Ha TT, et al. Among authors: mandelstam sa. Genes (Basel). 2023 Jul 31;14(8):1565. doi: 10.3390/genes14081565. Genes (Basel). 2023. PMID: 37628618 Free PMC article.
Pediatric ocular sonography.
Silva CT, Brockley CR, Crum A, Mandelstam SA. Silva CT, et al. Among authors: mandelstam sa. Semin Ultrasound CT MR. 2011 Feb;32(1):14-27. doi: 10.1053/j.sult.2010.09.005. Semin Ultrasound CT MR. 2011. PMID: 21277488 Review.
One-Stage, Limited-Resection Epilepsy Surgery for Bottom-of-Sulcus Dysplasia.
Macdonald-Laurs E, Maixner WJ, Bailey CA, Barton SM, Mandelstam SA, Yuan-Mou Yang J, Warren AEL, Kean MJ, Francis P, MacGregor D, D'Arcy C, Wrennall JA, Davidson A, Pope K, Leventer RJ, Freeman JL, Wray A, Jackson GD, Harvey AS. Macdonald-Laurs E, et al. Among authors: mandelstam sa. Neurology. 2021 Jul 13;97(2):e178-e190. doi: 10.1212/WNL.0000000000012147. Epub 2021 May 4. Neurology. 2021. PMID: 33947776
Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy.
Pederick DT, Richards KL, Piltz SG, Kumar R, Mincheva-Tasheva S, Mandelstam SA, Dale RC, Scheffer IE, Gecz J, Petrou S, Hughes JN, Thomas PQ. Pederick DT, et al. Among authors: mandelstam sa. Neuron. 2018 Jan 3;97(1):59-66.e5. doi: 10.1016/j.neuron.2017.12.005. Neuron. 2018. PMID: 29301106 Free article.
Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome.
Brown NJ, Ye Z, Stutterd C, Jayasinghe SI, Schneider A, Mullen S, Mandelstam SA, Hildebrand MS. Brown NJ, et al. Among authors: mandelstam sa. Cold Spring Harb Mol Case Stud. 2021 Dec 9;7(6):a006127. doi: 10.1101/mcs.a006127. Print 2021 Dec. Cold Spring Harb Mol Case Stud. 2021. PMID: 34588213 Free PMC article.
GRIN2A: an aptly named gene for speech dysfunction.
Turner SJ, Mayes AK, Verhoeven A, Mandelstam SA, Morgan AT, Scheffer IE. Turner SJ, et al. Among authors: mandelstam sa. Neurology. 2015 Feb 10;84(6):586-93. doi: 10.1212/WNL.0000000000001228. Epub 2015 Jan 16. Neurology. 2015. PMID: 25596506 Free PMC article.
30 results