Matalon R - Search Results

1

Cell-Based Therapy for Canavan Disease Using Human iPSC-Derived NPCs and OPCs.

Feng L, Chao J, Tian E, Li L, Ye P, Zhang M, Chen X, Cui Q, Sun G, Zhou T, Felix G, Qin Y, Li W, Meza ED, Klein J, Ghoda L, Hu W, Luo Y, Dang W, Hsu D, Gold J, Goldman SA, Matalon R, Shi Y. Feng L, et al. Among authors: matalon r. Adv Sci (Weinh). 2020 Oct 29;7(23):2002155. doi: 10.1002/advs.202002155. eCollection 2020 Dec. Adv Sci (Weinh). 2020. PMID: 33304759 Free PMC article.

2

Therapeutic development for Canavan disease using patient iPSCs introduced with the wild-type ASPA gene.

Chao J, Feng L, Ye P, Chen X, Cui Q, Sun G, Zhou T, Tian E, Li W, Hu W, Riggs AD, Matalon R, Shi Y. Chao J, et al. Among authors: matalon r. iScience. 2022 May 11;25(6):104391. doi: 10.1016/j.isci.2022.104391. eCollection 2022 Jun 17. iScience. 2022. PMID: 35637731 Free PMC article.

3

Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings.

Matalon RM, Michals-Matalon K. Matalon RM, et al. Front Biosci. 2000 Mar 1;5:D307-11. doi: 10.2741/matalon. Front Biosci. 2000. PMID: 10704428 Review.

4

Fragile X syndrome.

Hayes EW, Matalon R. Hayes EW, et al. Among authors: matalon r. Pediatrics. 2009 Aug;124(2):790-2. doi: 10.1542/peds.2009-0569. Epub 2009 Jul 5. Pediatrics. 2009. PMID: 19581265 No abstract available.

5

Gene therapy for metachromatic leukodystrophy.

Ohashi T, Watabe K, Sato Y, Saito I, Barranger JA, Matalon R, Eto Y. Ohashi T, et al. Among authors: matalon r. Acta Paediatr Jpn. 1996 Apr;38(2):193-201. doi: 10.1111/j.1442-200x.1996.tb03468.x. Acta Paediatr Jpn. 1996. PMID: 8677802

6

Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder.

Bhat G, LaGrave D, Millson A, Herriges J, Lamb AN, Matalon R. Bhat G, et al. Among authors: matalon r. Eur J Med Genet. 2016 Sep;59(9):470-3. doi: 10.1016/j.ejmg.2016.05.014. Epub 2016 May 27. Eur J Med Genet. 2016. PMID: 27238888

7

Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications.

Szafranski P, Golla S, Jin W, Fang P, Hixson P, Matalon R, Kinney D, Bock HG, Craigen W, Smith JL, Bi W, Patel A, Wai Cheung S, Bacino CA, Stankiewicz P. Szafranski P, et al. Among authors: matalon r. Eur J Hum Genet. 2015 Jul;23(7):915-21. doi: 10.1038/ejhg.2014.217. Epub 2014 Oct 15. Eur J Hum Genet. 2015. PMID: 25315662 Free PMC article.

8

When should children be tested for genetic diseases?

Trott AA, Matalon R. Trott AA, et al. Among authors: matalon r. Pediatrics. 2009 Oct;124(4):e807-8. doi: 10.1542/peds.2009-1498. Epub 2009 Sep 21. Pediatrics. 2009. PMID: 19770173 No abstract available.

9

Persistence of müllerian duct structures in a genetic male with distal monosomy 10q.

Tosur M, Geary CA, Matalon R, Radhakrishnan RS, Swischuk LE, Tarry WF, Dong J, Lee PD. Tosur M, et al. Among authors: matalon r. Am J Med Genet A. 2015 Apr;167A(4):791-6. doi: 10.1002/ajmg.a.37014. Am J Med Genet A. 2015. PMID: 25820398

10

Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly.

Meyertholen K, Ravnan JB, Matalon R. Meyertholen K, et al. Among authors: matalon r. Mol Syndromol. 2012 Jun;3(1):25-9. doi: 10.1159/000339177. Epub 2012 Jun 13. Mol Syndromol. 2012. PMID: 25759628 Free PMC article.

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