Huehne K - Search Results

1

Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations.

Brockmann K, Dreha-Kulaczewski S, Dechent P, Bönnemann C, Helms G, Kyllerman M, Brück W, Frahm J, Huehne K, Gärtner J, Rautenstrauss B. Brockmann K, et al. Among authors: huehne k. J Neurol. 2008 Jul;255(7):1049-58. doi: 10.1007/s00415-008-0847-1. Epub 2008 Apr 21. J Neurol. 2008. PMID: 18425620 Free article.

2

A novel mutation of myelin protein zero associated with late-onset predominantly axonal Charcot-Marie-Tooth disease.

Marttila M, Rautenstrauss B, Huehne K, Laitinen V, Majamaa K, Kärppä M. Marttila M, et al. Among authors: huehne k. J Neurol. 2012 Aug;259(8):1585-9. doi: 10.1007/s00415-011-6382-5. Epub 2012 Jan 6. J Neurol. 2012. PMID: 22222859

3

Novel human pathological mutations. Gene symbol: PMP22. Disease: Charcot-Marie-Tooth syndrome type 1A.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):545. Hum Genet. 2007. PMID: 18380017 No abstract available.

4

Novel human pathological mutations. Gene symbol: MPZ. Disease: Charcot-Marie-Tooth syndrome type 1B.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):545-6. Hum Genet. 2007. PMID: 18380018 No abstract available.

5

Novel human pathological mutations. Gene symbol: GJB1. Disease: Charcot-Marie-Tooth syndrome type X.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):546. Hum Genet. 2007. PMID: 18380019 No abstract available.

6

Novel human pathological mutations. Gene symbol: GJB1. Disease: Charcot-Marie-Tooth syndrome type X.

Rautenstrauss B, Huehne K, Kraus C, Thiel C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):548. Hum Genet. 2007. PMID: 18380022 No abstract available.

7

Novel human pathological mutations. Gene symbol: MPZ. Disease: Charcot-Marie-Tooth syndrome type X.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):547. Hum Genet. 2007. PMID: 18380024 No abstract available.

8

Novel human pathological mutations. Gene symbol: GJB1. Disease: Charcot-Marie-Tooth syndrome type 1B.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):547. Hum Genet. 2007. PMID: 18380026 No abstract available.

9

Novel human pathological mutations. Gene symbol: GJB1. Disease: Charcot-Marie-Tooth syndrome type X.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):547. Hum Genet. 2007. PMID: 18380028 No abstract available.

10

Novel human pathological mutations. Gene symbol: GJB1. Disease: Charcot-Marie-Tooth syndrome type X.

Rautenstrauss B, Huehne K, Thiel C, Kraus C. Rautenstrauss B, et al. Among authors: huehne k. Hum Genet. 2007 Dec;122(5):547. Hum Genet. 2007. PMID: 18380031 No abstract available.

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