Scherer SS - Search Results

1

Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

Thomas FP, Guergueltcheva V, Gondim FA, Tournev I, Rao CV, Ishpekova B, Kinsella LJ, Pan Y, Geller TJ, Litvinenko I, De Jonghe P, Scherer SS, Jordanova A. Thomas FP, et al. Among authors: scherer ss. J Neurol. 2016 Mar;263(3):467-76. doi: 10.1007/s00415-015-7989-8. Epub 2016 Jan 2. J Neurol. 2016. PMID: 26725087

2

The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.

Taylor RA, Simon EM, Marks HG, Scherer SS. Taylor RA, et al. Among authors: scherer ss. Neurology. 2003 Dec 9;61(11):1475-8. doi: 10.1212/01.wnl.0000095960.48964.25. Neurology. 2003. PMID: 14663027 No abstract available.

3

Molecular genetics of X-linked Charcot-Marie-Tooth disease.

Kleopa KA, Scherer SS. Kleopa KA, et al. Among authors: scherer ss. Neuromolecular Med. 2006;8(1-2):107-22. doi: 10.1385/nmm:8:1-2:107. Neuromolecular Med. 2006. PMID: 16775370 Review.

4

A patient with neurofibromatosis type 1 and Charcot-Marie-Tooth disease type 1B.

Lancaster E, Elman LB, Scherer SS. Lancaster E, et al. Among authors: scherer ss. Muscle Nerve. 2010 Apr;41(4):555-8. doi: 10.1002/mus.21546. Muscle Nerve. 2010. PMID: 19918771 Free PMC article.

5

A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.

Yum SW, Zhang J, Mo K, Li J, Scherer SS. Yum SW, et al. Among authors: scherer ss. Ann Neurol. 2009 Dec;66(6):759-70. doi: 10.1002/ana.21728. Ann Neurol. 2009. PMID: 20039262 Free PMC article.

6

Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy.

Vavlitou N, Sargiannidou I, Markoullis K, Kyriacou K, Scherer SS, Kleopa KA. Vavlitou N, et al. Among authors: scherer ss. J Neuropathol Exp Neurol. 2010 Sep;69(9):945-58. doi: 10.1097/NEN.0b013e3181efa658. J Neuropathol Exp Neurol. 2010. PMID: 20720503 Free PMC article.

7

Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia.

Lancaster E, Huijbers MG, Bar V, Boronat A, Wong A, Martinez-Hernandez E, Wilson C, Jacobs D, Lai M, Walker RW, Graus F, Bataller L, Illa I, Markx S, Strauss KA, Peles E, Scherer SS, Dalmau J. Lancaster E, et al. Among authors: scherer ss. Ann Neurol. 2011 Feb;69(2):303-11. doi: 10.1002/ana.22297. Ann Neurol. 2011. PMID: 21387375 Free PMC article.

8

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Kleopa KA, Abrams CK, Scherer SS. Kleopa KA, et al. Among authors: scherer ss. Brain Res. 2012 Dec 3;1487:198-205. doi: 10.1016/j.brainres.2012.03.068. Epub 2012 Jul 6. Brain Res. 2012. PMID: 22771394 Free PMC article. Review.

9

X-linked Charcot-Marie-Tooth disease.

Scherer SS, Kleopa KA. Scherer SS, et al. J Peripher Nerv Syst. 2012 Dec;17 Suppl 3(0 3):9-13. doi: 10.1111/j.1529-8027.2012.00424.x. J Peripher Nerv Syst. 2012. PMID: 23279425 Free PMC article. Review.

10

A novel AARS mutation in a family with dominant myeloneuropathy.

Motley WW, Griffin LB, Mademan I, Baets J, De Vriendt E, De Jonghe P, Antonellis A, Jordanova A, Scherer SS. Motley WW, et al. Among authors: scherer ss. Neurology. 2015 May 19;84(20):2040-7. doi: 10.1212/WNL.0000000000001583. Epub 2015 Apr 22. Neurology. 2015. PMID: 25904691 Free PMC article.

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