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  1. Pubblicazioni

HEMOGLOBIN

Rivista
Codice:
E075890
ISSN:
0363-0269
  • Dati Generali

Dati Generali

Pubblicazioni (32)

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A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A)
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A new electrophoretically silent, fetal hemoglobin variant: Hb F-Calabria [Ggamma118(GH1)Phe->Leu]
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A search for anomalies in the zeta, alpha, beta, and gamma-globin gene arrangement in normal Black, Italian, Turkish, and Spanish newborns. Hemoglobin, 13:45-65, 1989.
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A simple approach to the determination of the gamma chain composition of Hb F in adult human blood samples
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A simple approach to the determination of the gamma chain composition of Hb F in adult human samples.
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A study of the switch of fetal hemoglobin in newborn erythrocytes fractionated by density gradient
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A study of the switch of fetal hemoglobin in newborn erytrocytes fractionated by density gradient.
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Abnormal gamma globin gene arrangements in Sardinians.
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Biochemical and molecular aspects of beta-thalassemia types in North Sardinia.
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Characterization by DNA sequencing of the Hb F-Columbus-GA [Ggamma94(FG1)Asp->Asn] observed in Sardinian Newborn
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Haematological and biosynthetic features of beta°-thalassemia with an associated alpha-thalassemia heterozygosity in Sardinia
Articolo
Hb F-Avellino [Gγ41(C7)Phe → Leu; HBG2: c.124 T > C]: A New Hemoglobin Variant Observed In A Healthy Newborn.
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Hb F-Emirates [GGAMMA59(E3)Lys->Glu] observed in a family of Sardinian ancestry and characterized by DNA sequencing
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Hb F-Porto Torres [Aγ75(E19)Ile Thr, 136(H14)Ala Ser]: A novel variant of the Aγ chain having two substitutions, one being that of Hb F-Sardinia
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Hb Hamilton [beta11(A8)Val->Ile] in Sardinia.
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Hb Sassari or [alpha126(H9)Asp->His] observed in a family from Northern Sardinia.
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Hb TIGRAYE [B79(EF3)aSP--His] IN A CAUCASIAN FAMILY FROM SARDINIA
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Hb Tigraye [beta79(EF3)Asp®His)] in a Caucasian Family from Sardinia
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Hematological and biosynthetic features of betao-thalassemia with an associated beta-thalassemia heterozygosity in Sardinia.
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Hemoglobin F-Sassari: a novel Ggamma variant with a threonine residue in position gamma75 characterized by mass spectrometric techniques
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Hemoglobin G-Waimanalo [alpha64(E13Asp->Asn] observed in a Caucasian family
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Hemoglobin Hamilton [β11(A8)Val→Ile] in Sardinia
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Hemoglobin Lepore-Baltimore in a Sardinian family
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Hemoglobinopathies in Sardinia
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Homozygous for the betao39 mutation with thalassemia intermedia in Northern-Sardinia.
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Identification of Hb J-Sardegna [alpha50(CE8)His->Asp] by HPLC and its incidence in Northern Sardinia. Hemoglobin, 13:33-44, 1989.
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Molecular Characterization of β-Thalassemia Mutations in Central Vietnam
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Pistidda P., Cherchi L., Corda M., Hb Tigraye [beta79(EF3)Asp->His)] in a Caucasian Family from Sardinia
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Sheep Hb I variant, or betaB13(A10)Gly-Ser, in breeds from Corsica: detection by gene sequencing
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The gamma globin chain heterogeneity of the Sardinian newborn baby
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The gamma globin chain heterogeneity of the Sardinian newborn baby. Hemoglobin, 10:519-528, 1986.
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Two abnormal fetal hemoglobins found in the Sardinian population: the new Hb F-Osilo [Aγ119(GH2)Gly→Ser, GGC→AGC] and the Hb F-Paulinia [Gγ80(EF4)Asp→Tyr, GAT→ TAT] already described in the Brazilian population
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