18671190 25173405 20117750 25797487 20803648 25260206 24326961 34232380 23932106 22859694 22228622 25467432 - Search Results

Year	Number of Results
2008	1
2010	2
2012	2
2013	3
2014	3
2015	3
2021	1
2022	0

1

Mega-corpus callosum, polymicrogyria, and psychomotor retardation: confirmation of a syndromic entity.

Pierson TM, Zimmerman RA, Tennekoon GI, Bönnemann CG. Pierson TM, et al. Neuropediatrics. 2008 Apr;39(2):123-7. doi: 10.1055/s-2008-1081218. Neuropediatrics. 2008. PMID: 18671190

2

Corpus callosum thickness in children: an MR pattern-recognition approach on the midsagittal image.

Andronikou S, Pillay T, Gabuza L, Mahomed N, Naidoo J, Hlabangana LT, du Plessis V, Prabhu SP. Andronikou S, et al. Pediatr Radiol. 2015 Feb;45(2):258-72. doi: 10.1007/s00247-014-2998-9. Epub 2014 Aug 31. Pediatr Radiol. 2015. PMID: 25173405 Review.

3

Mega-corpus callosum, polymicrogyria, and psychomotor retardation syndrome.

Bindu PS, Taly AB, Sinha S, Bharath RD. Bindu PS, et al. Pediatr Neurol. 2010 Feb;42(2):129-32. doi: 10.1016/j.pediatrneurol.2009.09.012. Pediatr Neurol. 2010. PMID: 20117750

4

Timing in neural maturation: arrest, delay, precociousness, and temporal determination of malformations.

Sarnat HB, Philippart M, Flores-Sarnat L, Wei XC. Sarnat HB, et al. Pediatr Neurol. 2015 May;52(5):473-86. doi: 10.1016/j.pediatrneurol.2015.01.020. Epub 2015 Feb 9. Pediatr Neurol. 2015. PMID: 25797487 Review.

5

Megalencephaly, mega corpus callosum, and complete lack of motor development: delineation of a rare syndrome.

Hengst M, Tücke J, Zerres K, Blaum M, Häusler M. Hengst M, et al. Am J Med Genet A. 2010 Sep;152A(9):2360-4. doi: 10.1002/ajmg.a.33577. Am J Med Genet A. 2010. PMID: 20803648

6

Polymicrogyria, Large Corpus Callosum and Psychomotor Retardation in Four-Year-Old Girl: Potential Association Based on MR Findings. A Case Report and Literature Review.

Budai C, Moscato G, Patruno F, Leonardi M, Maffei M. Budai C, et al. Neuroradiol J. 2014 Oct;27(5):590-4. doi: 10.15274/NRJ-2014-10065. Epub 2014 Sep 25. Neuroradiol J. 2014. PMID: 25260206 Free PMC article. Review.

7

Syndrome of megalencephaly, mega corpus callosum, and complete lack of motor development: exploring the phenotype.

Agarwal V, Mukherjee SB, Gulati P, Aneja S. Agarwal V, et al. Clin Dysmorphol. 2013 Oct;22(4):164-168. doi: 10.1097/MCD.0000000000000009. Clin Dysmorphol. 2013. PMID: 24326961 No abstract available.

8

Genomics of human congenital hydrocephalus.

Kundishora AJ, Singh AK, Allington G, Duy PQ, Ryou J, Alper SL, Jin SC, Kahle KT. Kundishora AJ, et al. Childs Nerv Syst. 2021 Nov;37(11):3325-3340. doi: 10.1007/s00381-021-05230-8. Epub 2021 Jul 7. Childs Nerv Syst. 2021. PMID: 34232380

9

Biallelic SZT2 mutations cause infantile encephalopathy with epilepsy and dysmorphic corpus callosum.

Basel-Vanagaite L, Hershkovitz T, Heyman E, Raspall-Chaure M, Kakar N, Smirin-Yosef P, Vila-Pueyo M, Kornreich L, Thiele H, Bode H, Lagovsky I, Dahary D, Haviv A, Hubshman MW, Pasmanik-Chor M, Nürnberg P, Gothelf D, Kubisch C, Shohat M, Macaya A, Borck G. Basel-Vanagaite L, et al. Am J Hum Genet. 2013 Sep 5;93(3):524-9. doi: 10.1016/j.ajhg.2013.07.005. Epub 2013 Aug 8. Am J Hum Genet. 2013. PMID: 23932106 Free PMC article.

10

Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome: a case report.

Kariminejad A, Radmanesh F, Rezayi AR, Tonekaboni SH, Gleeson JG. Kariminejad A, et al. J Child Neurol. 2013 May;28(5):651-7. doi: 10.1177/0883073812448530. Epub 2012 Aug 1. J Child Neurol. 2013. PMID: 22859694

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