Zarate YA - Search Results

1

Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome.

Lewis H, Samanta D, Örsell JL, Bosanko KA, Rowell A, Jones M, Dale RC, Taravath S, Hahn CD, Krishnakumar D, Chagnon S, Keller S, Hagebeuk E, Pathak S, Bebin EM, Arndt DH, Alexander JJ, Mainali G, Coppola G, Maclean J, Sparagana S, McNamara N, Smith DM, Raggio V, Cruz M, Fernández-Jaén A, Kava MP, Emrick L, Fish JL, Vanderver A, Helman G, Pierson TM, Zarate YA. Lewis H, et al. Among authors: zarate ya. Pediatr Neurol. 2020 Nov;112:94-100. doi: 10.1016/j.pediatrneurol.2020.04.006. Epub 2020 Apr 13. Pediatr Neurol. 2020. PMID: 32446642

2

Description of the first case of adenomyomatosis of the gallbladder in an infant.

Zarate YA, Bosanko KA, Jarasvaraparn C, Vengoechea J, McDonough EM. Zarate YA, et al. Case Rep Pediatr. 2014;2014:248369. doi: 10.1155/2014/248369. Epub 2014 Jun 15. Case Rep Pediatr. 2014. PMID: 25024860 Free PMC article.

3

Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.

Zarate YA, Perry H, Ben-Omran T, Sellars EA, Stein Q, Almureikhi M, Simmons K, Klein O, Fish J, Feingold M, Douglas J, Kruer MC, Si Y, Mao R, McKnight D, Gibellini F, Retterer K, Slavotinek A. Zarate YA, et al. Am J Med Genet A. 2015 May;167A(5):1026-32. doi: 10.1002/ajmg.a.36849. Am J Med Genet A. 2015. PMID: 25885067

4

Phenotypic modifications of patients with full chromosome aneuploidies and concurrent suspected or confirmed second diagnoses.

Zarate YA, Bosanko KA, Bhoj E, Ganetzky R, Starr LJ, Zackai EH, Schaefer GB. Zarate YA, et al. Am J Med Genet A. 2015 Sep;167A(9):2168-75. doi: 10.1002/ajmg.a.37126. Epub 2015 Apr 25. Am J Med Genet A. 2015. PMID: 25914130 Free PMC article.

5

An infant with ash-leaf and café au lait spots: a case of double phakomatosis.

Samanta D, Bosanko KB, Zarate YA. Samanta D, et al. Among authors: zarate ya. Acta Neurol Belg. 2017 Mar;117(1):323-324. doi: 10.1007/s13760-016-0638-x. Epub 2016 Apr 4. Acta Neurol Belg. 2017. PMID: 27043227 No abstract available.

6

COL1A1 and COL1A2 sequencing results in cohort of patients undergoing evaluation for potential child abuse.

Zarate YA, Clingenpeel R, Sellars EA, Tang X, Kaylor JA, Bosanko K, Linam LE, Byers PH. Zarate YA, et al. Am J Med Genet A. 2016 Jul;170(7):1858-62. doi: 10.1002/ajmg.a.37664. Epub 2016 Apr 19. Am J Med Genet A. 2016. PMID: 27090748

7

First clinical report of an infant with microcephaly and CASC5 mutations.

Zarate YA, Kaylor JA, Bosanko K, Lau S, Vargas J, Gao H. Zarate YA, et al. Am J Med Genet A. 2016 Aug;170(8):2215-8. doi: 10.1002/ajmg.a.37726. Epub 2016 May 5. Am J Med Genet A. 2016. PMID: 27149178 No abstract available.

8

SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.

Zarate YA, Fish JL. Zarate YA, et al. Am J Med Genet A. 2017 Feb;173(2):327-337. doi: 10.1002/ajmg.a.38022. Epub 2016 Oct 24. Am J Med Genet A. 2017. PMID: 27774744 Free PMC article. Review.

9

Severe Metabolic Acidosis and Hepatopathy due to Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate.

Sellars EA, Balmakund T, Bosanko K, Nichols BL, Kahler SG, Zarate YA. Sellars EA, et al. Among authors: zarate ya. Neuropediatrics. 2017 Apr;48(2):108-110. doi: 10.1055/s-0036-1593984. Epub 2016 Nov 22. Neuropediatrics. 2017. PMID: 27875839

10

Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.

Zarate YA, Kalsner L, Basinger A, Jones JR, Li C, Szybowska M, Xu ZL, Vergano S, Caffrey AR, Gonzalez CV, Dubbs H, Zackai E, Millan F, Telegrafi A, Baskin B, Person R, Fish JL, Everman DB. Zarate YA, et al. Clin Genet. 2017 Oct;92(4):423-429. doi: 10.1111/cge.12982. Epub 2017 Mar 7. Clin Genet. 2017. PMID: 28139846

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