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SNCA variants are associated with increased risk for multiple system atrophy.
Ann Neurol. 2009 May;65(5):610-4. doi: 10.1002/ana.21685.
Ann Neurol. 2009.
PMID: 19475667
Free PMC article.
Mutational analysis of parkin and PINK1 in multiple system atrophy.
Brooks JA, Houlden H, Melchers A, Islam AJ, Ding J, Li A, Paudel R, Revesz T, Holton JL, Wood N, Lees A, Singleton AB, Scholz SW.
Brooks JA, et al. Among authors: melchers a.
Neurobiol Aging. 2011 Mar;32(3):548.e5-7. doi: 10.1016/j.neurobiolaging.2009.11.020. Epub 2010 Jan 19.
Neurobiol Aging. 2011.
PMID: 20034704
Free PMC article.
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THAP1 mutations (DYT6) are an additional cause of early-onset dystonia.
Houlden H, Schneider SA, Paudel R, Melchers A, Schwingenschuh P, Edwards M, Hardy J, Bhatia KP.
Houlden H, et al. Among authors: melchers a.
Neurology. 2010 Mar 9;74(10):846-50. doi: 10.1212/WNL.0b013e3181d5276d.
Neurology. 2010.
PMID: 20211909
Free PMC article.
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Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.
Dale RC, Melchers A, Fung VS, Grattan-Smith P, Houlden H, Earl J.
Dale RC, et al. Among authors: melchers a.
Dev Med Child Neurol. 2010 Jun;52(6):583-6. doi: 10.1111/j.1469-8749.2010.03619.x. Epub 2010 Feb 19.
Dev Med Child Neurol. 2010.
PMID: 20187889
Free article.
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An Aboriginal-led consortium approach to chronic disease action for health equity and holistic wellbeing.
Morey K, Pearson O, Sivak L, Brown K, Mejia G, Colmer K, Melchers A, Keech W, Brown A.
Morey K, et al. Among authors: melchers a.
Health Promot J Austr. 2023 Jul;34(3):634-643. doi: 10.1002/hpja.765. Epub 2023 Jun 29.
Health Promot J Austr. 2023.
PMID: 37386720
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A systematic proteomic study of irradiated DNA repair deficient Nbn-mice.
Melchers A, Stöckl L, Radszewski J, Anders M, Krenzlin H, Kalischke C, Scholz R, Jordan A, Nebrich G, Klose J, Sperling K, Digweed M, Demuth I.
Melchers A, et al.
PLoS One. 2009;4(5):e5423. doi: 10.1371/journal.pone.0005423. Epub 2009 May 1.
PLoS One. 2009.
PMID: 19412544
Free PMC article.
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An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.
Demuth I, Frappart PO, Hildebrand G, Melchers A, Lobitz S, Stöckl L, Varon R, Herceg Z, Sperling K, Wang ZQ, Digweed M.
Demuth I, et al. Among authors: melchers a.
Hum Mol Genet. 2004 Oct 15;13(20):2385-97. doi: 10.1093/hmg/ddh278. Epub 2004 Aug 27.
Hum Mol Genet. 2004.
PMID: 15333589
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