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                             13 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Comment on the article “Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri” by van den Munckhof et al. Prescott, Trine E.
2011
13 1 p. 103-104
artikel
2 Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort Maher, B. H.
2012
13 1 p. 97-101
artikel
3 Distinct DNA binding and transcriptional repression characteristics related to different ARX mutations Cho, Ginam
2012
13 1 p. 23-29
artikel
4 Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1 Kaut, Oliver
2012
13 1 p. 87-91
artikel
5 Genotype–phenotype correlation in interstitial 6q deletions: a report of 12 new cases Rosenfeld, Jill A.
2011
13 1 p. 31-47
artikel
6 Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri Munckhof, Pepijn van den
2011
13 1 p. 1-7
artikel
7 Independent replication of STAT3 association with multiple sclerosis risk in a large German case–control sample Lill, Christina M.
2011
13 1 p. 83-86
artikel
8 Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Bauer, Peter
2012
13 1 p. 73-76
artikel
9 Neuroferritinopathy: a new inborn error of iron metabolism Keogh, Michael J.
2012
13 1 p. 93-96
artikel
10 New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseases Beyer, Katrin
2011
13 1 p. 61-72
artikel
11 Pathomechanistic characterization of two exonic L1CAM variants located in trans in an obligate carrier of X-linked hydrocephalus Marx, Mariola
2011
13 1 p. 49-59
artikel
12 Restriction of trophic factors and nutrients induces PARKIN expression Klinkenberg, M.
2011
13 1 p. 9-21
artikel
13 Vincristine exacerbates asymptomatic Charcot–Marie–Tooth disease with a novel EGR2 mutation Nakamura, Tomonori
2012
13 1 p. 77-82
artikel
                             13 gevonden resultaten
 
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