Epplen JT - Search Results

1

Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literature.

Koch R, Scholz M, Nelen MR, Schwechheimer K, Epplen JT, Harders AG. Koch R, et al. Among authors: epplen jt. J Neurosurg. 1999 Apr;90(4):776-9. doi: 10.3171/jns.1999.90.4.0776. J Neurosurg. 1999. PMID: 10193626 Review.

2

Association of serotonin-1A and -2A receptor promoter polymorphisms with depressive symptoms, functional recovery, and pain in patients 6 months after lumbar disc surgery.

Lebe M, Hasenbring MI, Schmieder K, Jetschke K, Harders A, Epplen JT, Hoffjan S, Kötting J. Lebe M, et al. Among authors: epplen jt. Pain. 2013 Mar;154(3):377-384. doi: 10.1016/j.pain.2012.11.017. Epub 2012 Dec 7. Pain. 2013. PMID: 23318131

3

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.

Schöls L, Krüger R, Amoiridis G, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: epplen jt. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):67-73. doi: 10.1136/jnnp.64.1.67. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436730 Free PMC article.

4

Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Schöls L, Amoiridis G, Epplen JT, Langkafel M, Przuntek H, Riess O. Schöls L, et al. Among authors: epplen jt. J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):466-70. doi: 10.1136/jnnp.61.5.466. J Neurol Neurosurg Psychiatry. 1996. PMID: 8937340 Free PMC article.

5

Autonomic nervous system function in Huntington's disease.

Andrich J, Schmitz T, Saft C, Postert T, Kraus P, Epplen JT, Przuntek H, Agelink MW. Andrich J, et al. Among authors: epplen jt. J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):726-31. doi: 10.1136/jnnp.72.6.726. J Neurol Neurosurg Psychiatry. 2002. PMID: 12023413 Free PMC article.

6

Apolipoprotein E genotypes do not influence the age of onset in Huntington's disease.

Saft C, Andrich JE, Brune N, Gencik M, Kraus PH, Przuntek H, Epplen JT. Saft C, et al. Among authors: epplen jt. J Neurol Neurosurg Psychiatry. 2004 Dec;75(12):1692-6. doi: 10.1136/jnnp.2003.022756. J Neurol Neurosurg Psychiatry. 2004. PMID: 15548484 Free PMC article.

7

Molecular genetics of inherited diseases involving human chromosome 4.

Riess O, Schulz H, Träger T, Schmitt I, Epplen JT. Riess O, et al. Among authors: epplen jt. Cas Lek Cesk. 1995 Feb 15;134(4):108-16. Cas Lek Cesk. 1995. PMID: 7712535

8

Genetic background of apparently idiopathic sporadic cerebellar ataxia.

Schöls L, Szymanski S, Peters S, Przuntek H, Epplen JT, Hardt C, Riess O. Schöls L, et al. Among authors: epplen jt. Hum Genet. 2000 Aug;107(2):132-7. doi: 10.1007/s004390000346. Hum Genet. 2000. PMID: 11030410

9

Novel KIF7 Mutation in a Tunisian Boy with Acrocallosal Syndrome: Case Report and Review of the Literature.

Ibisler A, Hehr U, Barth A, Koch M, Epplen JT, Hoffjan S. Ibisler A, et al. Among authors: epplen jt. Mol Syndromol. 2015 Oct;6(4):173-80. doi: 10.1159/000439414. Epub 2015 Oct 7. Mol Syndromol. 2015. PMID: 26648833 Free PMC article.

10

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O. Schöls L, et al. Among authors: epplen jt. Ann Neurol. 1997 Dec;42(6):924-32. doi: 10.1002/ana.410420615. Ann Neurol. 1997. PMID: 9403486

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