Klein C - Search Results

1

Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene Review.

Weissbach A, Pauly MG, Herzog R, Hahn L, Halmans S, Hamami F, Bolte C, Camargos S, Jeon B, Kurian MA, Opladen T, Brüggemann N, Huppertz HJ, König IR, Klein C, Lohmann K. Weissbach A, et al. Among authors: klein c. Mov Disord. 2022 Feb;37(2):237-252. doi: 10.1002/mds.28874. Epub 2021 Dec 15. Mov Disord. 2022. PMID: 34908184 Review.

2

Paroxysmal choreoathetosis in a patient with idiopathic basal ganglia calcification, chorea, and dystonia.

Klein C, Vieregge P, Kömpf D. Klein C, et al. Mov Disord. 1997 Mar;12(2):254-5. doi: 10.1002/mds.870120223. Mov Disord. 1997. PMID: 9087991 No abstract available.

3

Concordant late onset of craniocervical dystonia in a pair of monozygotic twins.

Sieberer MG, Vieregge P, Klein C, Ozelius LJ, Wandinger KP. Sieberer MG, et al. Among authors: klein c. Mov Disord. 1999 Nov;14(6):1040-3. doi: 10.1002/1531-8257(199911)14:6<1040::aid-mds1025>3.0.co;2-9. Mov Disord. 1999. PMID: 10584687 No abstract available.

4

Genetics of primary dystonia.

Klein C, Breakefield XO, Ozelius LJ. Klein C, et al. Semin Neurol. 1999;19(3):271-80. doi: 10.1055/s-2008-1040843. Semin Neurol. 1999. PMID: 12194383 Review.

5

Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia.

Klein C, Hedrich K, Kabakçi K, Mohrmann K, Wiegers K, Landt O, Hagenah J, Schwinger E, Pramstaller PP, Ozelius LJ, Gucuyener K, Aysun S, Demir E. Klein C, et al. Neurology. 2002 Dec 10;59(11):1783-6. doi: 10.1212/01.wnl.0000035629.04791.3f. Neurology. 2002. PMID: 12473771

6

Focal dystonia as a presenting sign of spinocerebellar ataxia 17.

Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C. Hagenah JM, et al. Among authors: klein c. Mov Disord. 2004 Feb;19(2):217-20. doi: 10.1002/mds.10600. Mov Disord. 2004. PMID: 14978680

7

Genetic heterogeneity in ten families with myoclonus-dystonia.

Schüle B, Kock N, Svetel M, Dragasevic N, Hedrich K, De Carvalho Aguiar P, Liu L, Kabakci K, Garrels J, Meyer EM, Berisavac I, Schwinger E, Kramer PL, Ozelius LJ, Klein C, Kostic V. Schüle B, et al. Among authors: klein c. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1181-5. doi: 10.1136/jnnp.2003.027177. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258227 Free PMC article.

8

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.

Hagenah J, Saunders-Pullman R, Hedrich K, Kabakci K, Habermann K, Wiegers K, Mohrmann K, Lohnau T, Raymond D, Vieregge P, Nygaard T, Ozelius LJ, Bressman SB, Klein C. Hagenah J, et al. Among authors: klein c. Neurology. 2005 Mar 8;64(5):908-11. doi: 10.1212/01.WNL.0000152839.50258.A2. Neurology. 2005. PMID: 15753436

9

Co-occurrence of restless legs syndrome and Parkin mutations in two families.

Adel S, Djarmati A, Kabakci K, Pichler I, Eskelson C, Lohnau T, Kock N, Hagenah J, Hedrich K, Schwinger E, Kramer PL, Pramstaller PP, Klein C. Adel S, et al. Among authors: klein c. Mov Disord. 2006 Feb;21(2):258-63. doi: 10.1002/mds.20690. Mov Disord. 2006. PMID: 16161156

10

Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?

Djarmati A, Hedrich K, Svetel M, Lohnau T, Schwinger E, Romac S, Pramstaller PP, Kostić V, Klein C. Djarmati A, et al. Among authors: klein c. Mov Disord. 2006 Sep;21(9):1526-30. doi: 10.1002/mds.20977. Mov Disord. 2006. PMID: 16755580

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