Epplen C - Search Results

1

[Promoting remyelination as a future therapeutic principle in multiple sclerosis?].

Pöhlau D, Aktas O, Epplen C, Hartung HP, Hoffmann V, Przuntek H. Pöhlau D, et al. Among authors: epplen c. Nervenarzt. 1998 Oct;69(10):841-50. doi: 10.1007/s001150050352. Nervenarzt. 1998. PMID: 9834472 Review. German.

2

Genetic predisposition to multiple sclerosis as revealed by immunoprinting.

Epplen C, Jäckel S, Santos EJ, D'Souza M, Poehlau D, Dotzauer B, Sindern E, Haupts M, Rüde KP, Weber F, Stöver J, Poser S, Gehler W, Malin JP, Przuntek H, Epplen JT. Epplen C, et al. Among authors: epplen jt. Ann Neurol. 1997 Mar;41(3):341-52. doi: 10.1002/ana.410410309. Ann Neurol. 1997. PMID: 9066355 Clinical Trial.

3

Friedreich's ataxia. Revision of the phenotype according to molecular genetics.

Schöls L, Amoiridis G, Przuntek H, Frank G, Epplen JT, Epplen C. Schöls L, et al. Among authors: epplen jt, epplen c. Brain. 1997 Dec;120 ( Pt 12):2131-40. doi: 10.1093/brain/120.12.2131. Brain. 1997. PMID: 9448568

4

[Genetic components in autoimmune diseases].

Epplen C. Epplen C. Internist (Berl). 1999 May;40(5):469-75. doi: 10.1007/s001080050360. Internist (Berl). 1999. PMID: 10407756 Review. German. No abstract available.

5

Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?

Epplen JT, Buitkamp J, Epplen C, Mäueler W, Riess O. Epplen JT, et al. Among authors: epplen c. Electrophoresis. 1995 May;16(5):683-90. doi: 10.1002/elps.11501601111. Electrophoresis. 1995. PMID: 7588545 Review.

6

On simple repetitive DNA sequences and complex diseases.

Epplen C, Santos EJ, Mäueler W, van Helden P, Epplen JT. Epplen C, et al. Among authors: epplen jt. Electrophoresis. 1997 Aug;18(9):1577-85. doi: 10.1002/elps.1150180916. Electrophoresis. 1997. PMID: 9378125 Review.

7

Immunoprinting reveals different genetic bases for (auto)immuno diseases.

Epplen C, Buitkamp J, Rumpf H, D'Souza M, Epplen JT. Epplen C, et al. Among authors: epplen jt. Electrophoresis. 1995 Sep;16(9):1693-7. doi: 10.1002/elps.11501601281. Electrophoresis. 1995. PMID: 8582358 Review.

8

Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes.

Jaeckel S, Epplen JT, Kauth M, Miterski B, Tschentscher F, Epplen C. Jaeckel S, et al. Among authors: epplen c. Electrophoresis. 1998 Dec;19(18):3055-61. doi: 10.1002/elps.1150191802. Electrophoresis. 1998. PMID: 9932793 Review.

9

An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene.

Ristow M, Giannakidou E, Hebinck J, Busch K, Vorgerd M, Kotzka J, Knebel B, Mueller-Berghaus J, Epplen C, Pfeiffer A, Kahn CR, Doria A, Krone W, Mueller-Wieland D. Ristow M, et al. Among authors: epplen c. Diabetes. 1998 May;47(5):851-4. doi: 10.2337/diabetes.47.5.851. Diabetes. 1998. PMID: 9588463

10

Towards a fingerprint method covering the immunological genome.

Gomolka M, Schwaiger W, Weyers E, Epplen C, Buitkamp J, Epplen JT. Gomolka M, et al. Among authors: epplen jt, epplen c. Electrophoresis. 1992 Sep-Oct;13(9-10):623-5. doi: 10.1002/elps.11501301127. Electrophoresis. 1992. PMID: 1459078 No abstract available.

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