Sanner G - Search Results

1

Detailed clinical description of four patients with 1.3 and 2.1 Mb chromosome imbalances derived from a familial t(12;17)(q24.33;q25.3).

Schoumans J, Sanner G, Nordenskjöld M, Anderlid BM. Schoumans J, et al. Among authors: sanner g. Am J Med Genet A. 2005 Apr 30;134(3):254-8. doi: 10.1002/ajmg.a.30611. Am J Med Genet A. 2005. PMID: 15704131

2

[A renaissance for physical therapy in the treatment of cerebral palsy. Therapeutic methods in cerebral palsy].

Forssberg H, Sanner G, Rösblad B. Forssberg H, et al. Among authors: sanner g. Lakartidningen. 1998 Apr 8;95(15):1660-4. Lakartidningen. 1998. PMID: 9599470 Review. Swedish. No abstract available.

3

[In spite of a new law about support to persons with certain physical disabilities. "Adult rehabilitation is necessary for young adults"].

Sanner G, Lagerkvist B. Sanner G, et al. Lakartidningen. 1994 May 4;91(18):1835-8, 1843. Lakartidningen. 1994. PMID: 8189929 Review. Swedish. No abstract available.

4

[Deficient care of children with functional disabilities. Insecure relationship between child health services and parents].

Janson S, Risberg K, Sanner G. Janson S, et al. Among authors: sanner g. Lakartidningen. 1996 May 22;93(21):2057-60. Lakartidningen. 1996. PMID: 8649097 Swedish. No abstract available.

5

[Joint hypermobility, skin hyper-elasticity, connective tissue fragility: classical symptoms of Ehlers-Danlos syndrome].

Häggblom L, Sanner G. Häggblom L, et al. Among authors: sanner g. Lakartidningen. 1995 Dec 13;92(50):4809-13. Lakartidningen. 1995. PMID: 8538298 Swedish. No abstract available.

6

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: sanner 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.

7

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: sanner g. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258

8

[The remineralization of the vertebral metastases of breast carcinoma after radiotherapy].

Wachenfeld I, Sanner G, Böttcher HD, Kollath J. Wachenfeld I, et al. Among authors: sanner g. Strahlenther Onkol. 1996 Jun;172(6):332-41. Strahlenther Onkol. 1996. PMID: 8677507 German.

9

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: sanner g. Clin Genet. 1994 Feb;45(2):88-92. doi: 10.1111/j.1399-0004.1994.tb04000.x. Clin Genet. 1994. PMID: 8004804

10

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: sanner g. Brain Dev. 1993 Jul-Aug;15(4):295-8. doi: 10.1016/0387-7604(93)90027-6. Brain Dev. 1993. PMID: 8250153

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