Forsgren L - Search Results

1

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: forsgren l. 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

2

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: forsgren l. Neurology. 2002 Dec 10;59(11):1804-7. doi: 10.1212/01.wnl.0000036617.04943.96. Neurology. 2002. PMID: 12473779

3

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: forsgren l. Neurogenetics. 2011 May;12(2):137-43. doi: 10.1007/s10048-011-0274-9. Epub 2011 Feb 8. Neurogenetics. 2011. PMID: 21301909

4

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. Among authors: forsgren l. Hum Mol Genet. 1995 Aug;4(8):1441-5. doi: 10.1093/hmg/4.8.1441. Hum Mol Genet. 1995. PMID: 7581386

5

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: forsgren l. 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.

6

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: forsgren l. Hum Mol Genet. 1998 Feb;7(2):171-6. doi: 10.1093/hmg/7.2.171. Hum Mol Genet. 1998. PMID: 9425223

7

A role for both wild-type and expanded ataxin-7 in transcriptional regulation.

Ström AL, Forsgren L, Holmberg M. Ström AL, et al. Among authors: forsgren l. Neurobiol Dis. 2005 Dec;20(3):646-55. doi: 10.1016/j.nbd.2005.04.018. Epub 2005 Jun 3. Neurobiol Dis. 2005. PMID: 15936949

8

Identification and characterization of Spinocerebellar Ataxia Type 7 (SCA7) isoform SCA7b in mice.

Ström AL, Forsgren L, Holmberg M. Ström AL, et al. Among authors: forsgren l. Biochim Biophys Acta. 2005 Dec 20;1731(3):149-53. doi: 10.1016/j.bbaexp.2005.10.004. Epub 2005 Nov 2. Biochim Biophys Acta. 2005. PMID: 16297465

9

Cloning and expression analysis of the murine homolog of the spinocerebellar ataxia type 7 (SCA7) gene.

Ström AL, Jonasson J, Hart P, Brännström T, Forsgren L, Holmberg M. Ström AL, et al. Among authors: forsgren l. Gene. 2002 Feb 20;285(1-2):91-9. doi: 10.1016/s0378-1119(02)00399-2. Gene. 2002. PMID: 12039035

10

[Growing genes cause neurological diseases].

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

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