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1
Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin
Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin
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Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin

Harteveld, Cornelis L. ; Pissard, Serge ; Korver, Anna M. H. ; Riou, Jean ; Legac, Eric ; Lansbergen, Gideon ; Pardijs, Inge L. ; Giordano, Piero C. ; Versteegh, Florens G. A.

Hemoglobin, 2016-09, Vol.40 (5), p.349-352 [Periódico revisado por pares]

England: Taylor & Francis

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2
Comments on "UV and UV/H2O2 Treatment: The Silver Bullet for By-product and Genotoxicity Formation in Water Production"
Comments on "UV and UV/H2O2 Treatment: The Silver Bullet for By-product and Genotoxicity Formation in Water Production"
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Comments on "UV and UV/H2O2 Treatment: The Silver Bullet for By-product and Genotoxicity Formation in Water Production"

Heringa, Minne B. ; Janssen, Paul J.C.M. ; van Benthem, Jan ; Versteegh, Ans F.M.

Ozone: science & engineering, 2013-11, Vol.35 (6), p.519-520 [Periódico revisado por pares]

Abingdon: Taylor & Francis

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3
The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant
The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant
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The First Case of Hb Groene Hart [α119(H2)Pro→Ser, CCT→TCT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant

Giordano, Piero C. ; Zweegman, Sonja ; Akkermans, Nicole ; Arkesteijn, Sandra G.J. ; van Delft, Peter ; Versteegh, Florens G.A. ; Wajcman, Henri ; Harteveld, Cornelis L.

Hemoglobin, 2007-01, Vol.31 (2), p.179-182 [Periódico revisado por pares]

England: Informa UK Ltd

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4
Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype
Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype
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Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype

Harteveld, Cornelis L. ; Versteegh, Florens G.A. ; Kok, Peter J.M.J. ; van Rooijen-Nijdam, Irene H. ; van Delft, Peter ; Giordano, Piero C.

Hemoglobin, 2006, Vol.30 (3), p.349-354 [Periódico revisado por pares]

England: Informa UK Ltd

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5
Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: A New α2 Chain Variant Observed in a Morrocan Family
Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: A New α2 Chain Variant Observed in a Morrocan Family
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Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: A New α2 Chain Variant Observed in a Morrocan Family

Versteegh, Florens G.A. ; Arkesteijn, Sandra G.J. ; Bakker-Verweij, Margreet ; Haanappel, Karola ; Delft, Peter van ; Phylipsen, Marion ; Kaufmann, Judith O. ; Kok, Peter J.M.J. ; Lansbergen, Gideon W.A. ; Giordano, Piero C. ; Harteveld, Cornelis L.

Hemoglobin, 2011-04, Vol.35 (2), p.97-102 [Periódico revisado por pares]

England: Informa Healthcare

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6
A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α-Thalassemia Deletions, in Three Independent Asian Cases
A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α-Thalassemia Deletions, in Three Independent Asian Cases
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A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α-Thalassemia Deletions, in Three Independent Asian Cases

Harteveld, Cornelis L. ; Wijermans, Pierre W. ; de Ree, Juliette E. L. M. ; Ter Hal, Pauline ; Van Delft, Peter ; Van Rooijen-Nijdam, Irene H. ; Rasp, Ellen ; Kok, Peter J. M. J. ; Souverijn, John H. M. ; Versteegh, Florens G. A. ; Giordano, Piero C.

Hemoglobin, 2004-01, Vol.28 (1), p.1-5 [Periódico revisado por pares]

England: Informa UK Ltd

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7
Hb Buffalo [α89(FG1)His→Gln (α1)], Observed Solely and in the Presence of an Hb S [β6(A3)Glu→Val] Heterozygosity
Hb Buffalo [α89(FG1)His→Gln (α1)], Observed Solely and in the Presence of an Hb S [β6(A3)Glu→Val] Heterozygosity
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Hb Buffalo [α89(FG1)His→Gln (α1)], Observed Solely and in the Presence of an Hb S [β6(A3)Glu→Val] Heterozygosity

Harteveld, Cornelis L. ; Van Delft, Peter ; Akkermans, Nicole ; Arkesteijn, Sandra ; Van Rooijen-Nijdam, Irene H. ; Kok, Peter J.M.J. ; Versteegh, Florens G.A. ; Giordano, Piero C.

Hemoglobin, 2004-01, Vol.28 (3), p.223-227 [Periódico revisado por pares]

England: Informa UK Ltd

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8
Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion
Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion
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Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion

Harteveld, Cornelis L ; Versteegh, Florens G A ; van Leer, Eduard H G ; Starreveld, Jaap S ; Kok, Peter J M J ; van Rooijen-Nijdam, Irene ; van Delft, Peter ; Zanella-Cleon, Isabelle ; Becchi, Michel ; Wajcman, Henri ; Giordano, Piero C

Hemoglobin, 2007, Vol.31 (3), p.313-323 [Periódico revisado por pares]

England: Informa Healthcare

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9
Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THE α 1-GLOBIN CHAIN IS ASSOCIATED WITH A MILD α -THALASSEMIA PHENOTYPE
Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THE α 1-GLOBIN CHAIN IS ASSOCIATED WITH A MILD α -THALASSEMIA PHENOTYPE
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Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THE α 1-GLOBIN CHAIN IS ASSOCIATED WITH A MILD α -THALASSEMIA PHENOTYPE

Harteveld, Cornelis L. ; Delft, Peter van ; Plug, Rob ; Versteegh, Florens G.A. ; Hagen, Balt ; Rooijen, Irene van ; Kok, Peter J.M.J. ; Wajcman, Henri ; Kister, Jean ; Giordano, Piero C.

Hemoglobin, 2002-01, Vol.26 (3), p.255-260 [Periódico revisado por pares]

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10
Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion
Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion

Harteveld, Cornelis L. ; Versteegh, Florens G.A. ; van Leer, Eduard H.G. ; Starreveld, Jaap S. ; Kok, Peter J.M.J. ; van Rooijen-Nijdam, Irene ; van Delft, Peter ; Zanella-Cleon, Isabelle ; Becchi, Michel ; Wajcman, Henri ; Giordano, Piero C.

Hemoglobin, 2007, Vol.31 (3), p.313-323 [Periódico revisado por pares]

Informa UK Ltd

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