Similar articles for PMID: 25612753

Year	Number of Results
1956	1
1984	1
1985	3
1988	1
1990	2
1991	1
1992	1
1994	2
1999	1
2002	2
2003	1
2004	1
2005	1
2006	2
2007	1
2008	7
2009	5
2010	6
2011	7
2012	5
2013	6
2014	4
2015	4
2016	2
2020	1
2024	0

1

A case of lissencephaly in a 5-month-old infant.

Syed AE. Syed AE. BMJ Case Rep. 2015 Jan 22;2015:bcr2014206522. doi: 10.1136/bcr-2014-206522. BMJ Case Rep. 2015. PMID: 25612753 Free PMC article. No abstract available.

2

Lissencephaly presenting with congenital hypothyroidism.

Kumar S, Suthar R, Panigrahi I, Marwaha RK. Kumar S, et al. J Pediatr Endocrinol Metab. 2013;26(11-12):1175-7. doi: 10.1515/jpem-2013-0102. J Pediatr Endocrinol Metab. 2013. PMID: 23751382

3

An 11-month-old boy with refractory epilepsy.

Chakrabarty B, Dubey R, Kumar A, Gulati S. Chakrabarty B, et al. J Clin Neurosci. 2014 May;21(5):835, 892. doi: 10.1016/j.jocn.2013.08.026. J Clin Neurosci. 2014. PMID: 24843868 No abstract available.

4

Re: Prenatal diagnosis of lissencephaly: a case report.

Gadodia A, Gupta P, Sharma R, Kumar S. Gadodia A, et al. J Clin Ultrasound. 2011 Feb;39(2):91-2. doi: 10.1002/jcu.20764. Epub 2010 Dec 6. J Clin Ultrasound. 2011. PMID: 21213334 No abstract available.

5

A case of isolated pachygyria with unusual clinical onset in the neonatal period.

Carpinato C, Palano GM, Sottile E, Di Bella D, Distefano G. Carpinato C, et al. Pediatr Med Chir. 2008 Jul-Aug;30(4):204-7. Pediatr Med Chir. 2008. PMID: 19216204

6

High frequency of genomic deletions--and a duplication--in the LIS1 gene in lissencephaly: implications for molecular diagnosis.

Mei D, Lewis R, Parrini E, Lazarou LP, Marini C, Pilz DT, Guerrini R. Mei D, et al. J Med Genet. 2008 Jun;45(6):355-61. doi: 10.1136/jmg.2007.056507. Epub 2008 Feb 19. J Med Genet. 2008. PMID: 18285425

7

Lissencephaly--not an uncommon cause of intractable seizure in children: report of 3 cases.

Ghosh T, Barik K, Nayek K, Ghosh M, Datta AK, Mitraniyogi S. Ghosh T, et al. J Indian Med Assoc. 2010 Feb;108(2):114-5. J Indian Med Assoc. 2010. PMID: 20839570

8

Large congenital melanocytic nevi presenting with lissencephaly with an absent corpus callosum.

Takano T, Morimoto M, Sakaue Y, Takeuchi Y, Aotani H, Ohno M. Takano T, et al. Congenit Anom (Kyoto). 2008 Jun;48(2):97-100. doi: 10.1111/j.1741-4520.2008.00186.x. Congenit Anom (Kyoto). 2008. PMID: 18452492

9

Severe semilobar holoprosencephaly and lissencephaly associated with cebocephaly in a newborn.

Oncel MY, Yurttutan N, Yurttutan S, Ozdemir R, Canpolat FE, Erdeve O, Oguz SS, Dilmen U. Oncel MY, et al. Genet Couns. 2012;23(3):341-6. Genet Couns. 2012. PMID: 23072180

10

Prenatal diagnosis of lissencephaly: a case report.

Aslan H, Gungorduk K, Yildirim D, Aslan O, Yildirim G, Ceylan Y. Aslan H, et al. J Clin Ultrasound. 2009 May;37(4):245-8. doi: 10.1002/jcu.20572. J Clin Ultrasound. 2009. PMID: 19260111

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