Young P - Search Results

1

A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.

Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P. Warnecke T, et al. Among authors: young p. Mov Disord. 2010 Mar 15;25(4):413-20. doi: 10.1002/mds.22949. Mov Disord. 2010. PMID: 20108356

2

Specific pattern of early white-matter changes in pure hereditary spastic paraplegia.

Duning T, Warnecke T, Schirmacher A, Schiffbauer H, Lohmann H, Mohammadi S, Young P, Deppe M. Duning T, et al. Among authors: young p. Mov Disord. 2010 Sep 15;25(12):1986-92. doi: 10.1002/mds.23211. Mov Disord. 2010. PMID: 20669295

3

A novel form of autosomal recessive hereditary spastic paraplegia caused by a new SPG7 mutation.

Warnecke T, Duning T, Schwan A, Lohmann H, Epplen JT, Young P. Warnecke T, et al. Among authors: young p. Neurology. 2007 Jul 24;69(4):368-75. doi: 10.1212/01.wnl.0000266667.91074.fe. Neurology. 2007. PMID: 17646629

4

Report of a novel mutation in the PMP22 gene causing an axonal neuropathy.

Gess B, Jeibmann A, Schirmacher A, Kleffner I, Schilling M, Young P. Gess B, et al. Among authors: young p. Muscle Nerve. 2011 Apr;43(4):605-9. doi: 10.1002/mus.21973. Epub 2011 Feb 17. Muscle Nerve. 2011. PMID: 21337347

5

Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition.

List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A. List J, et al. Among authors: young p. Cereb Cortex. 2011 Dec;21(12):2774-87. doi: 10.1093/cercor/bhr071. Epub 2011 Apr 29. Cereb Cortex. 2011. PMID: 21531778

6

Brainstem involvement as a cause of central sleep apnea: pattern of microstructural cerebral damage in patients with cerebral microangiopathy.

Duning T, Deppe M, Brand E, Stypmann J, Becht C, Heidbreder A, Young P. Duning T, et al. Among authors: young p. PLoS One. 2013 Apr 23;8(4):e60304. doi: 10.1371/journal.pone.0060304. Print 2013. PLoS One. 2013. PMID: 23637744 Free PMC article.

7

Dysphagia in X-linked bulbospinal muscular atrophy (Kennedy disease).

Warnecke T, Oelenberg S, Teismann I, Suntrup S, Hamacher C, Young P, Ringelstein EB, Dziewas R. Warnecke T, et al. Among authors: young p. Neuromuscul Disord. 2009 Oct;19(10):704-8. doi: 10.1016/j.nmd.2009.06.371. Epub 2009 Jul 17. Neuromuscul Disord. 2009. PMID: 19616433

8

Neuroimaging in Susac's syndrome: focus on DTI.

Kleffner I, Deppe M, Mohammadi S, Schwindt W, Sommer J, Young P, Ringelstein EB. Kleffner I, et al. Among authors: young p. J Neurol Sci. 2010 Dec 15;299(1-2):92-6. doi: 10.1016/j.jns.2010.08.028. Epub 2010 Sep 17. J Neurol Sci. 2010. PMID: 20850137

9

Excessive Daytime Sleepiness Is a Common Symptom in Fabry Disease.

Duning T, Deppe M, Keller S, Schiffbauer H, Stypmann J, Böntert M, Schaefer R, Young P. Duning T, et al. Among authors: young p. Case Rep Neurol. 2009 Jul 22;1(1):33-40. doi: 10.1159/000226792. Case Rep Neurol. 2009. PMID: 20847834 Free PMC article.

10

Early microstructural white matter changes in patients with HIV: a diffusion tensor imaging study.

Stubbe-Drger B, Deppe M, Mohammadi S, Keller SS, Kugel H, Gregor N, Evers S, Young P, Ringelstein EB, Arendt G, Knecht S, Husstedt IW; German Competence Network HIV/AIDS. Stubbe-Drger B, et al. Among authors: young p. BMC Neurol. 2012 May 1;12:23. doi: 10.1186/1471-2377-12-23. BMC Neurol. 2012. PMID: 22548835 Free PMC article.

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