| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22
|
Ouled Amar Ben Cheikh, Bouchra
|
|
2008
|
10 |
1 |
p. 35-42
|
artikel
|
| 2 |
Alzheimer’s disease risk variants show association with cerebrospinal fluid amyloid beta
|
Kauwe, John S. K.
|
|
2008
|
10 |
1 |
p. 13-17
|
artikel
|
| 3 |
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis
|
Stogmann, E.
|
|
2008
|
10 |
1 |
p. 73-77
|
artikel
|
| 4 |
Assessment of Alzheimer’s disease case–control associations using family-based methods
|
Schjeide, Brit-Maren M.
|
|
2008
|
10 |
1 |
p. 19-25
|
artikel
|
| 5 |
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis
|
Filonzi, Laura
|
|
2008
|
10 |
1 |
p. 65-72
|
artikel
|
| 6 |
Erratum to ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia
|
Vermeer, Sascha
|
|
2008
|
10 |
1 |
p. 87
|
artikel
|
| 7 |
Expression analysis of genes lying in the NF1 microdeletion interval points to four candidate modifiers for neurofibroma formation
|
Bartelt-Kirbach, B.
|
|
2008
|
10 |
1 |
p. 79-85
|
artikel
|
| 8 |
Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation
|
Skoglund, Lena
|
|
2008
|
10 |
1 |
p. 27-34
|
artikel
|
| 9 |
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization
|
Bauer, Peter
|
|
2008
|
10 |
1 |
p. 43-48
|
artikel
|
| 10 |
Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9–2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)
|
Herzfeld, Thilo
|
|
2008
|
10 |
1 |
p. 59-64
|
artikel
|
| 11 |
Molecular and functional analysis of the HEXB gene in Italian patients affected with Sandhoff disease: identification of six novel alleles
|
Zampieri, Stefania
|
|
2008
|
10 |
1 |
p. 49-58
|
artikel
|
| 12 |
MS and autoimmune disorders
|
Ebers, G. C.
|
|
2008
|
10 |
1 |
p. 1-3
|
artikel
|
| 13 |
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions
|
Hemminki, Kari
|
|
2008
|
10 |
1 |
p. 5-11
|
artikel
|
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