Holmberg M - Search Results

1

Adult onset idiopathic torsion dystonia is excluded from the DYT 1 region (9q34) in a Swedish family.

Holmgren G, Ozelius L, Forsgren L, Almay BG, Holmberg M, Kramer P, Fahn S, Breakefield XO. Holmgren G, et al. Among authors: holmberg m. J Neurol Neurosurg Psychiatry. 1995 Aug;59(2):178-81. doi: 10.1136/jnnp.59.2.178. J Neurol Neurosurg Psychiatry. 1995. PMID: 7629534 Free PMC article.

2

Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.

Johansson J, Forsgren L, Sandgren O, Brice A, Holmgren G, Holmberg M. Johansson J, et al. Among authors: holmberg m. Hum Mol Genet. 1998 Feb;7(2):171-6. doi: 10.1093/hmg/7.2.171. Hum Mol Genet. 1998. PMID: 9425223

3

Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1.

Carlsson A, Forsgren L, Nylander PO, Hellman U, Forsman-Semb K, Holmgren G, Holmberg D, Holmberg M. Carlsson A, et al. Among authors: holmberg d, holmberg m. Neurology. 2002 Dec 10;59(11):1804-7. doi: 10.1212/01.wnl.0000036617.04943.96. Neurology. 2002. PMID: 12473779

4

Exclusion of the juvenile myoclonic epilepsy gene EFHC1 as the cause of migraine on chromosome 6, but association to two rare polymorphisms in MEP1A and RHAG.

Norberg A, Forsgren L, Holmberg D, Holmberg M. Norberg A, et al. Among authors: holmberg d, holmberg m. Neurosci Lett. 2006 Mar 27;396(2):137-42. doi: 10.1016/j.neulet.2005.11.039. Epub 2005 Dec 27. Neurosci Lett. 2006. PMID: 16378686

5

A family with a hereditary form of torsion dystonia from northern Sweden treated with bilateral pallidal deep brain stimulation.

Blomstedt P, Hariz MI, Tisch S, Holmberg M, Bergenheim TA, Forsgren L. Blomstedt P, et al. Among authors: holmberg m. Mov Disord. 2009 Dec 15;24(16):2415-9. doi: 10.1002/mds.22842. Mov Disord. 2009. PMID: 19890997

6

A high-penetrance form of late-onset torsion dystonia maps to a novel locus (DYT21) on chromosome 2q14.3-q21.3.

Norgren N, Mattson E, Forsgren L, Holmberg M. Norgren N, et al. Among authors: holmberg m. Neurogenetics. 2011 May;12(2):137-43. doi: 10.1007/s10048-011-0274-9. Epub 2011 Feb 8. Neurogenetics. 2011. PMID: 21301909

7

Localization of autosomal dominant cerebellar ataxia associated with retinal degeneration and anticipation to chromosome 3p12-p21.1.

Holmberg M, Johansson J, Forsgren L, Heijbel J, Sandgren O, Holmgren G. Holmberg M, et al. Hum Mol Genet. 1995 Aug;4(8):1441-5. doi: 10.1093/hmg/4.8.1441. Hum Mol Genet. 1995. PMID: 7581386

8

Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study.

Drugge U, Holmberg M, Holmgren G, Almay BG, Linderholm H. Drugge U, et al. Among authors: holmberg m. J Med Genet. 1995 May;32(5):344-7. doi: 10.1136/jmg.32.5.344. J Med Genet. 1995. PMID: 7616539 Free PMC article.

9

Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1.

Forsgren L, Libelius R, Holmberg M, von Döbeln U, Wibom R, Heijbel J, Sandgren O, Holmgren G. Forsgren L, et al. Among authors: holmberg m. J Neurol Sci. 1996 Dec;144(1-2):91-8. doi: 10.1016/s0022-510x(96)00187-6. J Neurol Sci. 1996. PMID: 8994109

10

[Growing genes cause neurological diseases].

Johansson J, Holmgren G, Forsgren L, Holmberg M. Johansson J, et al. Among authors: holmberg m. Lakartidningen. 1999 Feb 24;96(8):897-900. Lakartidningen. 1999. PMID: 10089735 Review. Swedish.

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

532 results

Search Page

Filters