PubMed for id: 1644310

Year	Number of Results
1990	1
1991	2
1993	4
1994	5
1995	3
1996	2
1997	3
1998	13
1999	18
2000	13
2001	9
2002	10
2003	10
2004	10
2005	10
2006	12
2007	12
2008	18
2009	25
2010	28
2011	19
2012	17
2013	20
2014	13
2015	13
2016	13
2017	18
2018	10
2019	13
2020	13
2021	14
2022	16
2023	17
2024	6

1

X-linked neuronal migration disorders: Gender differences and insights for genetic screening.

Edey J, Soleimani-Nouri P, Dawson-Kavanagh A, Imran Azeem MS, Episkopou V. Edey J, et al. Int J Dev Neurosci. 2023 Nov;83(7):581-599. doi: 10.1002/jdn.10290. Epub 2023 Aug 13. Int J Dev Neurosci. 2023. PMID: 37574439 Review.

2

Double cortex syndrome (subcortical band heterotopia): A case report.

Afzal F, Tabassum S, Naeem A, Naeem F, Ahmad RU. Afzal F, et al. Radiol Case Rep. 2022 Dec 5;18(2):671-674. doi: 10.1016/j.radcr.2022.11.021. eCollection 2023 Feb. Radiol Case Rep. 2022. PMID: 36484065 Free PMC article.

3

[Combinatory use of central venous catheter and ethanol lock for a patient with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome].

Motoi H, Shimizu H, Fujiwara Y, Watanabe Y, Kato M, Takeshita S. Motoi H, et al. No To Hattatsu. 2016 Sep;48(5):347-50. No To Hattatsu. 2016. PMID: 30010278 Japanese.

4

Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndrome.

Damiano JA, Do H, Ozturk E, Burgess R, Kalnins R, Jones NC, Dobrovic A, Berkovic SF, Hildebrand MS. Damiano JA, et al. Epileptic Disord. 2017 Dec 1;19(4):450-455. doi: 10.1684/epd.2017.0944. Epileptic Disord. 2017. PMID: 29258966

5

[Subcortical laminar heterotopia 'double cortex syndrome'].

Teplyshova AM, Gaskin VV, Kustov GV, Gudkova AA, Luzin RV, Trifonov IS, Lebedeva AV. Teplyshova AM, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(9. Vyp. 2):75-79. doi: 10.17116/jnevro20171179275-79. Zh Nevrol Psikhiatr Im S S Korsakova. 2017. PMID: 29213043 Russian.

6

X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease.

Coman D, Fullston T, Shoubridge C, Leventer R, Wong F, Nazaretian S, Simpson I, Gecz J, McGillivray G. Coman D, et al. Child Neurol Open. 2017 Nov 7;4:2329048X17738625. doi: 10.1177/2329048X17738625. eCollection 2017 Jan-Dec. Child Neurol Open. 2017. PMID: 29152528 Free PMC article.

7

A Neonate with X-linked Lissencephaly with Ambiguous Genitalia.

Minocha P, Choudhary A, Shambhavi, Sitaraman S. Minocha P, et al. J Pediatr Neurosci. 2017 Jan-Mar;12(1):80-82. doi: 10.4103/jpn.JPN_122_16. J Pediatr Neurosci. 2017. PMID: 28553390 Free PMC article.

8

A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.

Tsai MH, Kuo PW, Myers CT, Li SW, Lin WC, Fu TY, Chang HY, Mefford HC, Chang YC, Tsai JW. Tsai MH, et al. Eur J Paediatr Neurol. 2016 Sep;20(5):788-94. doi: 10.1016/j.ejpn.2016.05.010. Epub 2016 May 30. Eur J Paediatr Neurol. 2016. PMID: 27292316

9

Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX.

Moey C, Topper S, Karn M, Johnson AK, Das S, Vidaurre J, Shoubridge C. Moey C, et al. Eur J Hum Genet. 2016 May;24(5):681-9. doi: 10.1038/ejhg.2015.176. Epub 2015 Aug 26. Eur J Hum Genet. 2016. PMID: 26306640 Free PMC article.

10

Double Cortex Syndrome (Subcortical Band Heterotopia): A Case Report.

Momen AA, Momen M. Momen AA, et al. Iran J Child Neurol. 2015 Spring;9(2):64-8. Iran J Child Neurol. 2015. PMID: 26221167 Free PMC article.

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