| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Analysis of linkage disequilibrium between the 5′ and 3′ haplotypes of the β-globin gene cluster in Mexican afromestizos
|
Magaña, María Teresa
|
|
2010
|
44 |
2 |
p. 89-94
6 p.
|
artikel
|
| 2 |
CD31+ T cells represent a functionally distinct vascular T cell phenotype
|
Kushner, Erich J.
|
|
2010
|
44 |
2 |
p. 74-78
5 p.
|
artikel
|
| 3 |
Compounds of the anthracycline family of antibiotics elevate human γ-globin expression both in erythroid cultures and in a transgenic mouse model
|
Spyrou, Pandelis
|
|
2010
|
44 |
2 |
p. 100-106
7 p.
|
artikel
|
| 4 |
Directed sibling donor cord blood banking for children with β-thalassemia major in Greece: Usage rate and outcome of transplantation for HLA-matched units
|
Goussetis, Evgenios
|
|
2010
|
44 |
2 |
p. 107-110
4 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2010
|
44 |
2 |
p. IFC-
1 p.
|
artikel
|
| 6 |
Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation
|
Neishabury, Maryam
|
|
2010
|
44 |
2 |
p. 95-99
5 p.
|
artikel
|
| 7 |
Glucose-6-phosphate dehydrogenase (G6PD) molecular variant deficiency: Identification in Panama pediatric population
|
Cossio – Gurrola, G.
|
|
2010
|
44 |
2 |
p. 115-116
2 p.
|
artikel
|
| 8 |
Guidelines for the restart of imiglucerase in patients with Gaucher disease: Recommendations from the European Working Group on Gaucher disease
|
Hollak, Carla E.M.
|
|
2010
|
44 |
2 |
p. 86-87
2 p.
|
artikel
|
| 9 |
Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region—A comparison of the bilirubin plasmatic levels in the different clinical forms
|
Rocha, Susana
|
|
2010
|
44 |
2 |
p. 117-119
3 p.
|
artikel
|
| 10 |
Molecular identification of the HLA-DRB1-DQB1 for diagnosis and follow-up of acute leukemias
|
Fernandes, Tania Aparecida Rodrigues
|
|
2010
|
44 |
2 |
p. 69-73
5 p.
|
artikel
|
| 11 |
Novel mutations of the DKC1 gene in individuals affected with dyskeratosis congenita
|
Rostamiani, K.
|
|
2010
|
44 |
2 |
p. 88-
1 p.
|
artikel
|
| 12 |
Perinatal lethal form of Gaucher disease. Clinical and molecular characterization of a Greek case
|
Michelakakis, Helen
|
|
2010
|
44 |
2 |
p. 82-83
2 p.
|
artikel
|
| 13 |
Prenatal diagnosis of hemophilia A, presenting a new mutation in the FVIII gene
|
He, Zhihui
|
|
2010
|
44 |
2 |
p. 124-125
2 p.
|
artikel
|
| 14 |
Proteinase-activated receptor (PAR1) polymorphic variant correlates with thrombocytopenia in Gaucher disease
|
Altarescu, Gheona
|
|
2010
|
44 |
2 |
p. 79-81
3 p.
|
artikel
|
| 15 |
Reaction of nitrite with human fetal oxyhemoglobin: A model simulation study with implications for blood flow regulation in sickle cell disease (SCD)
|
Salhany, James M.
|
|
2010
|
44 |
2 |
p. 111-114
4 p.
|
artikel
|
| 16 |
Recommendations for treating patients with Gaucher disease with emerging enzyme products
|
Cox, Timothy M.
|
|
2010
|
44 |
2 |
p. 84-85
2 p.
|
artikel
|
| 17 |
Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency
|
Abdallah, Hejer Elmahmoudi
|
|
2010
|
44 |
2 |
p. 120-123
4 p.
|
artikel
|
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