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Low frequency of RET mutations in Hirschsprung disease in Sweden.
Svensson PJ, Molander ML, Eng C, Anvret M, Nordenskjöld A. Svensson PJ, et al. Among authors: anvret m. Clin Genet. 1998 Jul;54(1):39-44. doi: 10.1111/j.1399-0004.1998.tb03691.x. Clin Genet. 1998. PMID: 9727738
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
Buervenich S, Carmine A, Galter D, Shahabi HN, Johnels B, Holmberg B, Ahlberg J, Nissbrandt H, Eerola J, Hellström O, Tienari PJ, Matsuura T, Ashizawa T, Wüllner U, Klockgether T, Zimprich A, Gasser T, Hanson M, Waseem S, Singleton A, McMahon FJ, Anvret M, Sydow O, Olson L. Buervenich S, et al. Among authors: anvret m. Arch Neurol. 2005 Jan;62(1):74-8. doi: 10.1001/archneur.62.1.74. Arch Neurol. 2005. PMID: 15642852
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's disease.
Belin AC, Ran C, Anvret A, Paddock S, Westerlund M, Håkansson A, Nissbrandt H, Söderkvist P, Dizdar N, Ahmadi A, Anvret M, Willows T, Sydow O, Galter D. Belin AC, et al. Among authors: anvret m. Neurosci Lett. 2012 Jul 26;522(1):30-5. doi: 10.1016/j.neulet.2012.06.007. Epub 2012 Jun 13. Neurosci Lett. 2012. PMID: 22704918
NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
Carmine A, Buervenich S, Galter D, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Chowdari KV, Nimgaonkar VL, Anvret M, Sydow O, Olson L. Carmine A, et al. Among authors: anvret m. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):51-7. doi: 10.1002/ajmg.b.20033. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12815740
Two NOTCH4 polymorphisms and their relation to schizophrenia susceptibility and different personality traits.
Carmine A, Chheda MG, Jönsson EG, Sedvall GC, Farde L, Gustavsson JP, Bergman H, Anvret M, Buervenich S, Olson L. Carmine A, et al. Among authors: anvret m. Psychiatr Genet. 2003 Mar;13(1):23-8. doi: 10.1097/00041444-200303000-00004. Psychiatr Genet. 2003. PMID: 12605097
Further evidence for an association of the paraoxonase 1 (PON1) Met-54 allele with Parkinson's disease.
Carmine A, Buervenich S, Sydow O, Anvret M, Olson L. Carmine A, et al. Among authors: anvret m. Mov Disord. 2002 Jul;17(4):764-6. doi: 10.1002/mds.10172. Mov Disord. 2002. PMID: 12210872
CTLA4 dimorphisms and the multiple sclerosis phenotype.
Masterman T, Ligers A, Zhang Z, Hellgren D, Salter H, Anvret M, Hillert J. Masterman T, et al. Among authors: anvret m. J Neuroimmunol. 2002 Oct;131(1-2):208-12. doi: 10.1016/s0165-5728(02)00274-6. J Neuroimmunol. 2002. PMID: 12458054
Effects of the mutant von Willebrand factor gene in von Willebrand disease.
Zhang Z, Lindstedt M, Blombäck M, Anvret M. Zhang Z, et al. Among authors: anvret m. Hum Genet. 1995 Oct;96(4):388-94. doi: 10.1007/BF00191794. Hum Genet. 1995. PMID: 7557958
Characterization and regulation of the nonerythroid porphobilinogen deaminase promoter.
Lundin G, Anvret M. Lundin G, et al. Among authors: anvret m. Biochem Biophys Res Commun. 1997 Feb 13;231(2):409-11. doi: 10.1006/bbrc.1997.6114. Biochem Biophys Res Commun. 1997. PMID: 9070289
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria.
Lee JS, Anvret M, Lindsten J, Lannfelt L, Gellerfors P, Wetterberg L, Floderus Y, Thunell S. Lee JS, et al. Among authors: anvret m. Hum Genet. 1988 Aug;79(4):379-81. doi: 10.1007/BF00282182. Hum Genet. 1988. PMID: 2900803
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