Holmgren G - Search Results

1

A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.

Klein C, Schilling K, Saunders-Pullman RJ, Garrels J, Breakefield XO, Brin MF, deLeon D, Doheny D, Fahn S, Fink JS, Forsgren L, Friedman J, Frucht S, Harris J, Holmgren G, Kis B, Kurlan R, Kyllerman M, Lang AE, Leung J, Raymond D, Robishaw JD, Sanner G, Schwinger E, Tabamo RE, Tagliati M. Klein C, et al. Among authors: holmgren g. Am J Hum Genet. 2000 Nov;67(5):1314-9. Epub 2000 Oct 5. Am J Hum Genet. 2000. PMID: 11022010 Free PMC article.

2

The gene for familial dystonia with myoclonic jerks responsive to alcohol is not located on the distal end of 9q.

Wahlström J, Ozelius L, Kramer P, Kyllerman M, Schuback D, Forsgren L, Holmgren G, Drugge U, Sanner G, Fahn S, et al. Wahlström J, et al. Among authors: holmgren g. Clin Genet. 1994 Feb;45(2):88-92. doi: 10.1111/j.1399-0004.1994.tb04000.x. Clin Genet. 1994. PMID: 8004804

3

Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.

Klein C, Gurvich N, Sena-Esteves M, Bressman S, Brin MF, Ebersole BJ, Fink S, Forsgren L, Friedman J, Grimes D, Holmgren G, Kyllerman M, Lang AE, de Leon D, Leung J, Prioleau C, Raymond D, Sanner G, Saunders-Pullman R, Vieregge P, Wahlström J, Breakefield XO, Kramer PL, Ozelius LJ, Sealfon SC. Klein C, et al. Among authors: holmgren g. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258

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

7

Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.

Schuback D, Kramer P, Ozelius L, Holmgren G, Forsgren L, Kyllerman M, Wahlström J, Craft CM, Nygaard T, Brin M, et al. Schuback D, et al. Among authors: holmgren g. Hum Genet. 1991 Jul;87(3):311-6. doi: 10.1007/BF00200910. Hum Genet. 1991. PMID: 1677923

8

Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation.

Kyllerman M, Forsgren L, Sanner G, Holmgren G, Wahlström J, Drugge U. Kyllerman M, et al. Among authors: holmgren g. Mov Disord. 1990;5(4):270-9. doi: 10.1002/mds.870050403. Mov Disord. 1990. PMID: 2259350

9

Early onset dystonia decreasing with development. Case report of two children with familial myoclonic dystonia.

Kyllerman M, Sanner G, Forsgren L, Holmgren G, Wahlström J. Kyllerman M, et al. Among authors: holmgren g. Brain Dev. 1993 Jul-Aug;15(4):295-8. doi: 10.1016/0387-7604(93)90027-6. Brain Dev. 1993. PMID: 8250153

10

Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

Dahl N, Goonewardena P, Malmgren H, Gustavson KH, Holmgren G, Seemanova E, Annerén G, Flood A, Pettersson U. Dahl N, et al. Among authors: holmgren g. Am J Hum Genet. 1989 Aug;45(2):304-9. Am J Hum Genet. 1989. PMID: 2569270 Free PMC article.

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