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                             15 results found
no title author magazine year volume issue page(s) type
1 Ablation of the Kell/Xk complex alters erythrocyte divalent cation homeostasis Rivera, Alicia
2013
50 2 p. 80-85
6 p.
article
2 A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone Ney-Garcia, Daniela Ribeiro
2013
50 2 p. 131-133
3 p.
article
3 A historical perspective on the development of the cytarabine (7days) and daunorubicin (3days) treatment regimen for acute myelogenous leukemia: 2013 the 40th anniversary of 7+3 Lichtman, Marshall A.
2013
50 2 p. 119-130
12 p.
article
4 Alpha Thalassaemia and extended alpha globin genes in Sri Lanka Suresh, Sasikala
2013
50 2 p. 93-98
6 p.
article
5 Ambroxol as a pharmacological chaperone for mutant glucocerebrosidase Bendikov-Bar, Inna
2013
50 2 p. 141-145
5 p.
article
6 Analysis of the genetic variants of glucose-6-phosphate dehydrogenase in inhabitants of the 4th Nile cataract region in Sudan Kempinska-Podhorodecka, Agnieszka
2013
50 2 p. 115-118
4 p.
article
7 Biological validation of bio-engineered red blood cell productions Giarratana, Marie-Catherine
2013
50 2 p. 69-79
11 p.
article
8 Combined chelation therapy with deferasirox and deferoxamine in thalassemia Lal, Ashutosh
2013
50 2 p. 99-104
6 p.
article
9 Commentary on “Pilot study using ambroxol as a pharmacological chaperone in type 1 Gaucher disease” by Zimran et al. Goker-Alpan, Ozlem
2013
50 2 p. 138-139
2 p.
article
10 Editorial Board 2013
50 2 p. IFC-
1 p.
article
11 ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic level Brown, Fiona C.
2013
50 2 p. 86-92
7 p.
article
12 Evolving features in type 3 Gaucher disease on long-term enzyme replacement therapy Elstein, Deborah
2013
50 2 p. 140-
1 p.
article
13 Pilot study using ambroxol as a pharmacological chaperone in type 1 Gaucher disease Zimran, Ari
2013
50 2 p. 134-137
4 p.
article
14 Two new class III G6PD variants [G6PD Tunis (c.920A>C: p.307Gln>Pro) and G6PD Nefza (c.968T>C: p.323 Leu>Pro)] and overview of the spectrum of mutations in Tunisia Benmansour, Ikbel
2013
50 2 p. 110-114
5 p.
article
15 Unexplained extreme hyperbilirubinemia among neonates in a multihospital healthcare system Christensen, Robert D.
2013
50 2 p. 105-109
5 p.
article
                             15 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands