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

Year Number of Results
2005 1
2006 1
2009 1
2010 1
2012 2
2013 1
2014 1
2016 1
2021 0
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9 results
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Page 1
Analysis of EEG patterns and genotypes in patients with Angelman syndrome.
Vendrame M, Loddenkemper T, Zarowski M, Gregas M, Shuhaiber H, Sarco DP, Morales A, Nespeca M, Sharpe C, Haas K, Barnes G, Glaze D, Kothare SV. Vendrame M, et al. Among authors: morales a. Epilepsy Behav. 2012 Mar;23(3):261-5. doi: 10.1016/j.yebeh.2011.11.027. Epub 2012 Feb 16. Epilepsy Behav. 2012. PMID: 22341959
Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease.
Pierce SB, Gulsuner S, Stapleton GA, Walsh T, Lee MK, Mandell JB, Morales A, Klevit RE, King MC, Rogers RC. Pierce SB, et al. Among authors: morales a. Cold Spring Harb Mol Case Stud. 2016 Jul;2(4):a001107. doi: 10.1101/mcs.a001107. Cold Spring Harb Mol Case Stud. 2016. PMID: 27551684 Free PMC article.
Vagus nerve stimulation for the management of seizures in children: an 8-year experience.
Coykendall DS, Gauderer MW, Blouin RR, Morales A. Coykendall DS, et al. Among authors: morales a. J Pediatr Surg. 2010 Jul;45(7):1479-83. doi: 10.1016/j.jpedsurg.2010.02.066. J Pediatr Surg. 2010. PMID: 20638528
Congenital livedo reticularis and recurrent strokes in two unrelated young children.
Mathias G, Cowley R, Morales A, Rogers RC. Mathias G, et al. Among authors: morales a. Clin Pediatr (Phila). 2006 May;45(4):367-72. doi: 10.1177/000992280604500411. Clin Pediatr (Phila). 2006. PMID: 16703162 No abstract available.
Microcephaly and congenital grouped pigmentation of the retinal pigment epithelium associated with submicroscopic deletions of 13q33.3-q34 and 11p15.4.
Siddiqui AM, Everman DB, Rogers RC, DuPont BR, Smith BT, Seaver LH, Morales A, Varn M, Cohen B, Traboulsi EI. Siddiqui AM, et al. Among authors: morales a. Ophthalmic Genet. 2009 Sep;30(3):136-41. doi: 10.1080/13816810903085263. Ophthalmic Genet. 2009. PMID: 19941418
Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutations.
Tay SK, Sacconi S, Akman HO, Morales JF, Morales A, De Vivo DC, Shanske S, Bonilla E, DiMauro S. Tay SK, et al. Among authors: morales a. J Child Neurol. 2005 Aug;20(8):670-4. doi: 10.1177/08830738050200080701. J Child Neurol. 2005. PMID: 16225813
On the support of scientific workflows over Pub/Sub brokers.
Morales A, Robles T, Alcarria R, Cedeño E. Morales A, et al. Sensors (Basel). 2013 Aug 20;13(8):10954-80. doi: 10.3390/s130810954. Sensors (Basel). 2013. PMID: 23966191 Free PMC article.
Enhancing evacuation plans with a situation awareness system based on end-user knowledge provision.
Morales A, Alcarria R, Martin D, Robles T. Morales A, et al. Sensors (Basel). 2014 Jun 24;14(6):11153-78. doi: 10.3390/s140611153. Sensors (Basel). 2014. PMID: 24961212 Free PMC article.
Enabling flexible and continuous capability invocation in mobile prosumer environments.
Alcarria R, Robles T, Morales A, López-de-Ipiña D, Aguilera U. Alcarria R, et al. Among authors: morales a. Sensors (Basel). 2012;12(7):8930-54. doi: 10.3390/s120708930. Epub 2012 Jun 28. Sensors (Basel). 2012. PMID: 23012526 Free PMC article.