Flores-Sarnat L - Search Results

1

Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype.

Abdel-Salam GM, Flores-Sarnat L, El-Ruby MO, Parboosingh J, Bridge P, Eid MM, El-Badry TH, Effat L, Curatolo P, Temtamy SA. Abdel-Salam GM, et al. Am J Med Genet A. 2011 Jan;155A(1):207-14. doi: 10.1002/ajmg.a.33777. Am J Med Genet A. 2011. PMID: 21204234

2

Hemimegalencephaly syndrome.

Flores-Sarnat L. Flores-Sarnat L. Handb Clin Neurol. 2008;87:153-76. doi: 10.1016/S0072-9752(07)87010-2. Handb Clin Neurol. 2008. PMID: 18809024 No abstract available.

3

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.

Yu TW, Mochida GH, Tischfield DJ, Sgaier SK, Flores-Sarnat L, Sergi CM, Topçu M, McDonald MT, Barry BJ, Felie JM, Sunu C, Dobyns WB, Folkerth RD, Barkovich AJ, Walsh CA. Yu TW, et al. Nat Genet. 2010 Nov;42(11):1015-20. doi: 10.1038/ng.683. Epub 2010 Oct 3. Nat Genet. 2010. PMID: 20890278 Free PMC article.

4

Deletion of chromosome 21 disturbs human brain morphogenesis.

Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, Korenberg JR. Yao G, et al. Genet Med. 2006 Jan;8(1):1-7. doi: 10.1097/01.gim.0000195892.60506.3f. Genet Med. 2006. PMID: 16418593 Free article.

5

Neuroembryology and brain malformations: an overview.

Sarnat HB, Flores-Sarnat L. Sarnat HB, et al. Handb Clin Neurol. 2013;111:117-28. doi: 10.1016/B978-0-444-52891-9.00012-9. Handb Clin Neurol. 2013. PMID: 23622157 Review.

6

Axes and gradients of the neural tube for a morphological/molecular genetic classification of nervous system malformations.

Flores-Sarnat L, Sarnat HB. Flores-Sarnat L, et al. Handb Clin Neurol. 2008;87:1-11. doi: 10.1016/S0072-9752(07)87001-1. Handb Clin Neurol. 2008. PMID: 18809015 No abstract available.

7

Hemimegalencephaly: part 2. Neuropathology suggests a disorder of cellular lineage.

Flores-Sarnat L, Sarnat HB, Dávila-Gutiérrez G, Alvarez A. Flores-Sarnat L, et al. J Child Neurol. 2003 Nov;18(11):776-85. doi: 10.1177/08830738030180111101. J Child Neurol. 2003. PMID: 14696906

8

Phenotype/genotype correlations in epidermal nevus syndrome as a neurocristopathy.

Flores-Sarnat L, Sarnat HB. Flores-Sarnat L, et al. Handb Clin Neurol. 2015;132:9-25. doi: 10.1016/B978-0-444-62702-5.00002-0. Handb Clin Neurol. 2015. PMID: 26564069 Review.

9

Hemimegalencephaly: foetal tauopathy with mTOR hyperactivation and neuronal lipidosis.

Sarnat H, Flores-Sarnat L, Crino P, Hader W, Bello-Espinosa L. Sarnat H, et al. Folia Neuropathol. 2012;50(4):330-45. doi: 10.5114/fn.2012.32363. Folia Neuropathol. 2012. PMID: 23319189 Free article.

10

Neuropathology of pediatric epilepsy.

Sarnat HB, Flores-Sarnat L. Sarnat HB, et al. Handb Clin Neurol. 2013;111:399-416. doi: 10.1016/B978-0-444-52891-9.00044-0. Handb Clin Neurol. 2013. PMID: 23622189 Review.

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