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 |