Lyons MJ - Search Results

1

Transgenerational Inheritance of Familial Lipomyelomeningocele.

Larrew T, Eskandari R, Holden KR, Chen A, Spellicy CJ, Jones JR, Lee JA, Lyons MJ. Larrew T, et al. Among authors: lyons mj. J Child Neurol. 2017 Dec;32(14):1118-1122. doi: 10.1177/0883073817736701. J Child Neurol. 2017. PMID: 29129155

2

Early onset alpha-mannosidosis with slow progression in three Hispanic males.

Lyons MJ, Wood T, Espinoza L, Stensland HM, Holden KR. Lyons MJ, et al. Dev Med Child Neurol. 2007 Nov;49(11):854-7. doi: 10.1111/j.1469-8749.2007.00854.x. Dev Med Child Neurol. 2007. PMID: 17979865 Free article.

3

Two percent of patients suspected of having Angelman syndrome have TCF4 mutations.

Takano K, Lyons M, Moyes C, Jones J, Schwartz CE. Takano K, et al. Clin Genet. 2010 Sep;78(3):282-8. doi: 10.1111/j.1399-0004.2010.01380.x. Epub 2010 Feb 10. Clin Genet. 2010. PMID: 20184619

4

Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.

Lyons MJ, Duron R, Molinero I, Sangiuolo F, Holden KR. Lyons MJ, et al. Pediatr Neurol. 2010 May;42(5):365-8. doi: 10.1016/j.pediatrneurol.2010.01.014. Pediatr Neurol. 2010. PMID: 20399394

5

Autism in two females with duplications involving Xp11.22-p11.23.

Edens AC, Lyons MJ, Duron RM, Dupont BR, Holden KR. Edens AC, et al. Among authors: lyons mj. Dev Med Child Neurol. 2011 May;53(5):463-6. doi: 10.1111/j.1469-8749.2010.03909.x. Epub 2011 Mar 21. Dev Med Child Neurol. 2011. PMID: 21418194 Free article.

6

LIS1 duplication: expanding the phenotype.

Lockrow JP, Holden KR, Dwivedi A, Matheus MG, Lyons MJ. Lockrow JP, et al. Among authors: lyons mj. J Child Neurol. 2012 Jun;27(6):791-5. doi: 10.1177/0883073811425972. Epub 2011 Dec 21. J Child Neurol. 2012. PMID: 22190508

7

Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.

Lyons MJ, Fuller JD, Montoya Mdel C, DuPont BR, Holden KR. Lyons MJ, et al. J Child Neurol. 2013 Apr;28(4):524-6. doi: 10.1177/0883073812446309. Epub 2012 Jun 29. J Child Neurol. 2013. PMID: 22752474

8

Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion.

Dean SJ, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Dean SJ, et al. Among authors: lyons mj. Pediatr Neurol. 2014 Jun;50(6):636-9. doi: 10.1016/j.pediatrneurol.2014.01.055. Epub 2014 Feb 10. Pediatr Neurol. 2014. PMID: 24725350

9

Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.

Mooneyham KA, Holden KR, Cathey S, Dwivedi A, Dupont BR, Lyons MJ. Mooneyham KA, et al. Among authors: lyons mj. Am J Med Genet A. 2014 Nov;164A(11):2887-91. doi: 10.1002/ajmg.a.36708. Epub 2014 Aug 13. Am J Med Genet A. 2014. PMID: 25123844

10

Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment.

Smith AW, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Smith AW, et al. Among authors: lyons mj. J Child Neurol. 2015 Mar;30(4):517-21. doi: 10.1177/0883073814545113. Epub 2014 Oct 7. J Child Neurol. 2015. PMID: 25296922

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