Young P - Search Results

1

Clinical features and molecular genetics of hereditary peripheral neuropathies.

Kuhlenbäumer G, Young P, Hünermund G, Ringelstein B, Stögbauer F. Kuhlenbäumer G, et al. Among authors: young p. J Neurol. 2002 Dec;249(12):1629-50. doi: 10.1007/s00415-002-0946-3. J Neurol. 2002. PMID: 12529785 Review.

2

A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.

Young P, Wiebusch H, Stögbauer F, Ringelstein B, Assmann G, Funke H. Young P, et al. Neurology. 1997 Feb;48(2):450-2. doi: 10.1212/wnl.48.2.450. Neurology. 1997. PMID: 9040737

3

Autosomal dominant burning feet syndrome.

Stögbauer F, Young P, Kuhlenbäumer G, Kiefer R, Timmerman V, Ringelstein EB, Wang JF, Schröder JM, Van Broeckhoven C, Weis J. Stögbauer F, et al. Among authors: young p. J Neurol Neurosurg Psychiatry. 1999 Jul;67(1):78-81. doi: 10.1136/jnnp.67.1.78. J Neurol Neurosurg Psychiatry. 1999. PMID: 10369826 Free PMC article.

4

Hereditary recurrent focal neuropathies: clinical and molecular features.

Stögbauer F, Young P, Kuhlenbäumer G, De Jonghe P, Timmerman V. Stögbauer F, et al. Among authors: young p. Neurology. 2000 Feb 8;54(3):546-51. doi: 10.1212/wnl.54.3.546. Neurology. 2000. PMID: 10680781

5

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.

Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: young p. J Neurol. 2001 Oct;248(10):861-5. doi: 10.1007/s004150170070. J Neurol. 2001. PMID: 11697522

6

Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene.

Kuhlenbäumer G, Young P, Oberwittler C, Hünermund G, Schirmacher A, Domschke K, Ringelstein B, Stögbauer F. Kuhlenbäumer G, et al. Among authors: young p. Neurology. 2002 Apr 23;58(8):1273-6. doi: 10.1212/wnl.58.8.1273. Neurology. 2002. PMID: 11971098

7

Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.

Kuhlenbäumer G, Lüdemann P, Schirmacher A, De Vriendt E, Hünermund G, Young P, Hund-Georgiadis M, Schuierer G, Möller H, Ringelstein EB, Van Broeckhoven C, Timmerman V, Stögbauer F. Kuhlenbäumer G, et al. Among authors: young p. Neurology. 2004 Jun 22;62(12):2203-8. doi: 10.1212/01.wnl.0000130485.89814.10. Neurology. 2004. PMID: 15210883

8

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy.

Hünermund G, Schirmacher A, Ringelstein B, Young P, Watts GD, Meuleman J, Nelis E, Chance PF, Timmerman V, Stögbauer F, Kuhlenbäumer G. Hünermund G, et al. Among authors: young p. Muscle Nerve. 2004 Apr;29(4):601-4. doi: 10.1002/mus.20009. Muscle Nerve. 2004. PMID: 15052627

9

Absence of mutations in the prion-protein gene in a large cohort of HMSN patients.

Koop O, Timmerman V, de Jonghe P, Ringelstein B, Young P, Kuhlenbäumer G. Koop O, et al. Among authors: young p. Neuromuscul Disord. 2005 Aug;15(8):549-51. doi: 10.1016/j.nmd.2005.06.007. Neuromuscul Disord. 2005. PMID: 16009550

10

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF. Kuhlenbäumer G, et al. Among authors: young p. Nat Genet. 2005 Oct;37(10):1044-6. doi: 10.1038/ng1649. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186812

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