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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1981 4
1982 1
1983 1
1984 1
1985 1
1986 2
1987 2
1988 5
1989 5
1990 7
1991 11
1992 15
1993 10
1994 13
1995 9
1996 4
1997 14
1998 9
1999 9
2000 5
2001 7
2002 4
2003 4
2005 2
2012 1
2023 0

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Search Results

146 results

Results by year

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Page 1
Welander distal myopathy--an overview.
Borg K, Ahlberg G, Anvret M, Edström L. Borg K, et al. Among authors: anvret m. Neuromuscul Disord. 1998 Apr;8(2):115-8. doi: 10.1016/s0960-8966(98)00008-x. Neuromuscul Disord. 1998. PMID: 9608565 Review.
394delTT: a Nordic cystic fibrosis mutation.
Schwartz M, Anvret M, Claustres M, Eiken HG, Eiklid K, Schaedel C, Stolpe L, Tranebjaerg L. Schwartz M, et al. Among authors: anvret m. Hum Genet. 1994 Feb;93(2):157-61. doi: 10.1007/BF00210602. Hum Genet. 1994. PMID: 7509310
Genetics of the Rett syndrome.
Anvret M, Wahlström J. Anvret M, et al. Brain Dev. 1992 May;14 Suppl:S101-3. Brain Dev. 1992. PMID: 1626621 Review.
Alcohol dehydrogenase alleles in Parkinson's disease.
Buervenich S, Sydow O, Carmine A, Zhang Z, Anvret M, Olson L. Buervenich S, et al. Among authors: anvret m. Mov Disord. 2000 Sep;15(5):813-8. doi: 10.1002/1531-8257(200009)15:5<813::aid-mds1008>;2-y. Mov Disord. 2000. PMID: 11009184
Mutation screening in Rett syndrome patients.
Xiang F, Buervenich S, Nicolao P, Bailey ME, Zhang Z, Anvret M. Xiang F, et al. Among authors: anvret m. J Med Genet. 2000 Apr;37(4):250-5. doi: 10.1136/jmg.37.4.250. J Med Genet. 2000. PMID: 10745042 Free PMC article.
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
Parental exposure to hydrocarbons in Prader-Willi syndrome.
Akefeldt A, Anvret M, Grandell U, Nordlinder R, Gillberg C. Akefeldt A, et al. Among authors: anvret m. Dev Med Child Neurol. 1995 Dec;37(12):1101-9. doi: 10.1111/j.1469-8749.1995.tb11971.x. Dev Med Child Neurol. 1995. PMID: 8566468
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
X chromosome linkage studies in familial Rett syndrome.
Curtis AR, Headland S, Lindsay S, Thomas NS, Boye E, Kamakari S, Roustan P, Anvret M, Wahlstrom J, McCarthy G, et al. Curtis AR, et al. Among authors: anvret m. Hum Genet. 1993 Jan;90(5):551-5. doi: 10.1007/BF00217457. Hum Genet. 1993. PMID: 8094068
146 results