| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A lung cancer gene GPC5 could also be crucial in breast cancer
|
Zhang, Changwen
|
|
2011
|
103 |
1 |
p. 104-105
2 p.
|
artikel
|
| 2 |
A polymorphism in the angiotensin II type 1 receptor gene has different effects on the risk of diabetic nephropathy in men and women
|
Möllsten, Anna
|
|
2011
|
103 |
1 |
p. 66-70
5 p.
|
artikel
|
| 3 |
Association study of MC4R with complex obesity and replication of the rs17782313 association signal
|
Beckers, Sigri
|
|
2011
|
103 |
1 |
p. 71-75
5 p.
|
artikel
|
| 4 |
Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice
|
Liegel, R.
|
|
2011
|
103 |
1 |
p. 51-59
9 p.
|
artikel
|
| 5 |
−1227C>T polymorphism in the pleiotrophin gene promoter influences bone mineral density in postmenopausal women
|
Mencej-Bedrač, Simona
|
|
2011
|
103 |
1 |
p. 76-80
5 p.
|
artikel
|
| 6 |
Editorial Board
|
|
|
2011
|
103 |
1 |
p. IFC-
1 p.
|
artikel
|
| 7 |
Genetic variation in the matrix metalloproteinase genes and diabetic nephropathy in type 1 diabetes
|
Kure, Masahiko
|
|
2011
|
103 |
1 |
p. 60-65
6 p.
|
artikel
|
| 8 |
Genetic variation of the ATP-binding cassette transporter A1 and susceptibility to coronary heart disease
|
Jiang, Zhihui
|
|
2011
|
103 |
1 |
p. 81-88
8 p.
|
artikel
|
| 9 |
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption
|
Shin, Daniel Sanghoon
|
|
2011
|
103 |
1 |
p. 33-37
5 p.
|
artikel
|
| 10 |
Improved assay for differential diagnosis between Pompe disease and acid α-glucosidase pseudodeficiency on dried blood spots
|
Shigeto, Shohei
|
|
2011
|
103 |
1 |
p. 12-17
6 p.
|
artikel
|
| 11 |
Maternal medium-chain acyl-CoA dehydrogenase deficiency identified by newborn screening
|
Leydiker, K.B.
|
|
2011
|
103 |
1 |
p. 92-95
4 p.
|
artikel
|
| 12 |
MicroRNA profiling of cystic fibrosis intestinal disease in mice
|
Bazett, Mark
|
|
2011
|
103 |
1 |
p. 38-43
6 p.
|
artikel
|
| 13 |
Molecular mechanism for stabilization of a mutant α-galactosidase A involving M51I amino acid substitution by imino sugars
|
Tsukimura, Takahiro
|
|
2011
|
103 |
1 |
p. 26-32
7 p.
|
artikel
|
| 14 |
Natural course of glutamine synthetase deficiency in a 3year old patient
|
Häberle, Johannes
|
|
2011
|
103 |
1 |
p. 89-91
3 p.
|
artikel
|
| 15 |
Neuroinflammatory and oxidative stress phenomena in MPS IIIA mouse model: The positive effect of long-term aspirin treatment
|
Arfi, Audrey
|
|
2011
|
103 |
1 |
p. 18-25
8 p.
|
artikel
|
| 16 |
Oral administration of recombinant human acid α-glucosidase reduces specific antibody formation against enzyme in mouse
|
Ohashi, T.
|
|
2011
|
103 |
1 |
p. 98-100
3 p.
|
artikel
|
| 17 |
Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency
|
Vellekoop, P.
|
|
2011
|
103 |
1 |
p. 96-97
2 p.
|
artikel
|
| 18 |
Pompe disease: Design, methodology, and early findings from the Pompe Registry
|
Byrne, Barry J.
|
|
2011
|
103 |
1 |
p. 1-11
11 p.
|
artikel
|
| 19 |
Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic)
|
Miller, Bradley S.
|
|
2011
|
103 |
1 |
p. 101-103
3 p.
|
artikel
|
| 20 |
Table of Contents
|
|
|
2011
|
103 |
1 |
p. iii-iv
nvt p.
|
artikel
|
| 21 |
Vascular pathology of medial arterial calcifications in NT5E deficiency: Implications for the role of adenosine in pseudoxanthoma elasticum
|
Markello, Thomas C.
|
|
2011
|
103 |
1 |
p. 44-50
7 p.
|
artikel
|
Tijdschrift beschrijving