Russell MB - Search Results

1

Herrmann A, Braathen GJ, Russell MB. Herrmann A, et al. Among authors: russell mb. Tidsskr Nor Laegeforen. 2005 Aug 11;125(15):2005-7. Tidsskr Nor Laegeforen. 2005. PMID: 16100538 Free article. Review. Norwegian.

2

Hereditary peripheral neuropathies diagnosed by next-generation sequencing.

Høyer H, Busk ØL, Holla ØL, Strand L, Russell MB, Skjelbred CF, Braathen GJ. Høyer H, et al. Among authors: russell mb. Tidsskr Nor Laegeforen. 2015 Nov 3;135(20):1838-44. doi: 10.4045/tidsskr.14.1002. eCollection 2015 Nov 3. Tidsskr Nor Laegeforen. 2015. PMID: 26534810 Free article. English, Norwegian.

3

[Cerebral cavernous malformations].

Koht J, Braathen GJ, Neubert D, Russell MB. Koht J, et al. Among authors: russell mb. Tidsskr Nor Laegeforen. 2005 Aug 11;125(15):2008-10. Tidsskr Nor Laegeforen. 2005. PMID: 16100539 Free article. Review. Norwegian.

4

Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing.

Høyer H, Braathen GJ, Busk ØL, Holla ØL, Svendsen M, Hilmarsen HT, Strand L, Skjelbred CF, Russell MB. Høyer H, et al. Among authors: russell mb. Biomed Res Int. 2014;2014:210401. doi: 10.1155/2014/210401. Epub 2014 Jun 16. Biomed Res Int. 2014. PMID: 25025039 Free PMC article.

5

Copy number variations in a population-based study of Charcot-Marie-Tooth disease.

Høyer H, Braathen GJ, Eek AK, Nordang GB, Skjelbred CF, Russell MB. Høyer H, et al. Among authors: russell mb. Biomed Res Int. 2015;2015:960404. doi: 10.1155/2015/960404. Epub 2015 Jan 8. Biomed Res Int. 2015. PMID: 25648254 Free PMC article.

6

Two novel connexin32 mutations cause early onset X-linked Charcot-Marie-Tooth disease.

Braathen GJ, Sand JC, Bukholm G, Russell MB. Braathen GJ, et al. Among authors: russell mb. BMC Neurol. 2007 Jul 9;7:19. doi: 10.1186/1471-2377-7-19. BMC Neurol. 2007. PMID: 17620124 Free PMC article.

7

MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.

Braathen GJ, Sand JC, Lobato A, Høyer H, Russell MB. Braathen GJ, et al. Among authors: russell mb. BMC Med Genet. 2010 Mar 29;11:48. doi: 10.1186/1471-2350-11-48. BMC Med Genet. 2010. PMID: 20350294 Free PMC article.

8

Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome.

Braathen GJ, Sand JC, Russell MB. Braathen GJ, et al. Among authors: russell mb. BMC Res Notes. 2010 Apr 12;3:99. doi: 10.1186/1756-0500-3-99. BMC Res Notes. 2010. PMID: 20385006 Free PMC article.

9

Corrigendum to "Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing".

Høyer H, Braathen GJ, Busk ØL, Holla ØL, Svendsen M, Hilmarsen HT, Strand L, Skjelbred CF, Russell MB. Høyer H, et al. Among authors: russell mb. Biomed Res Int. 2015;2015:314651. doi: 10.1155/2015/314651. Epub 2015 Oct 8. Biomed Res Int. 2015. PMID: 26558264 Free PMC article. No abstract available.

10

Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation.

Høyer H, Busk ØL, Esbensen QY, Røsby O, Hilmarsen HT, Russell MB, Nyman TA, Braathen GJ, Nilsen HL. Høyer H, et al. Among authors: russell mb. BMC Neurol. 2022 Aug 15;22(1):299. doi: 10.1186/s12883-022-02828-6. BMC Neurol. 2022. PMID: 35971119 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

232 results

Search Page

Filters