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

Year Number of Results
1991 2
1993 2
1994 2
1995 1
1996 3
1997 2
2001 2
2003 2
2004 3
2005 5
2006 2
2007 2
2008 1
2009 8
2010 1
2011 8
2012 11
2013 4
2014 11
2015 6
2016 4
2017 2
2018 2
2020 5
2021 4
2022 2
2024 0

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83 results

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Page 1
Focal Epilepsy in Individuals with Laron Syndrome.
Goldberg L, Laron Z, Kornreich L, Scheuerman O, Goldberg-Stern H, Kraus D. Goldberg L, et al. Among authors: goldberg stern h. Horm Res Paediatr. 2022;95(3):286-290. doi: 10.1159/000524350. Epub 2022 Mar 31. Horm Res Paediatr. 2022. PMID: 35358968 Free PMC article.
[Infantile spasms and modified hypsarrhythmia].
Halevy A, Kiviti S, Goldberg-Stern H, Shuper A. Halevy A, et al. Among authors: goldberg stern h. Harefuah. 2011 Apr;150(4):373-7, 418, 417. Harefuah. 2011. PMID: 22164920 Review. Hebrew.
An emerging 1q21.1 deletion-associated neurodevelopmental phenotype.
Basel-Vanagaite L, Goldberg-Stern H, Mimouni-Bloch A, Shkalim V, Böhm D, Kohlhase J. Basel-Vanagaite L, et al. Among authors: goldberg stern h. J Child Neurol. 2011 Jan;26(1):113-6. doi: 10.1177/0883073810377658. J Child Neurol. 2011. PMID: 21212457
[Startle disorders].
Goldberg-Stern H, Gadoth N. Goldberg-Stern H, et al. Harefuah. 1991 Nov 1;121(9):348-9. Harefuah. 1991. PMID: 1800292 Review. Hebrew. No abstract available.
Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy.
Spinelli E, Christensen KR, Bryant E, Schneider A, Rakotomamonjy J, Muir AM, Giannelli J, Littlejohn RO, Roeder ER, Schmidt B, Wilson WG, Marco EJ, Iwama K, Kumada S, Pisano T, Barba C, Vetro A, Brilstra EH, van Jaarsveld RH, Matsumoto N, Goldberg-Stern H, Carney PW, Andrews PI, El Achkar CM, Berkovic S, Rodan LH; Undiagnosed Diseases Network (UDN); McWalter K, Guerrini R, Scheffer IE, Mefford HC, Mandelstam S, Laux L, Millichap JJ, Guemez-Gamboa A, Nairn AC, Carvill GL. Spinelli E, et al. Among authors: goldberg stern h. Ann Neurol. 2021 Aug;90(2):274-284. doi: 10.1002/ana.26147. Epub 2021 Jul 13. Ann Neurol. 2021. PMID: 34185323 Free PMC article.
Detection of copy number variations in epilepsy using exome data.
Tsuchida N, Nakashima M, Kato M, Heyman E, Inui T, Haginoya K, Watanabe S, Chiyonobu T, Morimoto M, Ohta M, Kumakura A, Kubota M, Kumagai Y, Hamano SI, Lourenco CM, Yahaya NA, Ch'ng GS, Ngu LH, Fattal-Valevski A, Weisz Hubshman M, Orenstein N, Marom D, Cohen L, Goldberg-Stern H, Uchiyama Y, Imagawa E, Mizuguchi T, Takata A, Miyake N, Nakajima H, Saitsu H, Miyatake S, Matsumoto N. Tsuchida N, et al. Among authors: goldberg stern h. Clin Genet. 2018 Mar;93(3):577-587. doi: 10.1111/cge.13144. Epub 2018 Jan 25. Clin Genet. 2018. PMID: 28940419
Immunoglobulin treatment for severe childhood epilepsy.
Geva-Dayan K, Shorer Z, Menascu S, Linder I, Goldberg-Stern H, Heyman E, Lerman-Sagie T, Ben Zeev B, Kramer U. Geva-Dayan K, et al. Among authors: goldberg stern h. Pediatr Neurol. 2012 Jun;46(6):375-81. doi: 10.1016/j.pediatrneurol.2012.03.015. Pediatr Neurol. 2012. PMID: 22633633
83 results