LASTING HB-F REACTIVATION AND HB-A2 REDUCTION INDUCED BY THE TREATMENT OF HODGKINS-DISEASE IN A WOMAN HETEROZYGOUS FOR BETA-THALASSEMIA AND THE SWISS TYPE OF THE HETEROCELLULAR HEREDITARY PERSISTENCE OF HB F

被引：1

|

作者：

CECH, P ^{[1
]}

TESTA, U ^{[1
]}

DUBART, A ^{[1
]}

SCHNEIDER, P ^{[1
]}

BACHMANN, F ^{[1
]}

GUERRASIO, A ^{[1
]}

BEUZARD, Y ^{[1
]}

SCHMIDT, PM ^{[1
]}

CLEMENT, F ^{[1
]}

ROSA, J ^{[1
]}

机构：

[1] HOP HENRI MONDOR,INSERM,UNITE RECH ANEMIES 91,F-94010 CRETEIL,FRANCE

来源：

ACTA HAEMATOLOGICA | 1982年 / 67卷 / 04期

关键词：

D O I：

10.1159/000207075

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：275 / 284

页数：10

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ALTAY, C
GURGEY, A
[J]. JOURNAL OF MEDICAL GENETICS, 1985, 22 (03) : 205 - 212
[2] HETEROGENEITY OF DELTA,BETA-THALASSEMIA AND HEREDITARY PERSISTENCE OF HB F IN THE MEDITERRANEAN AREA
OTTOLENGHI, S
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GUIDA, S
CASINI, C
MERLI, S
MANTOVANI, R
TERRAGNI, F
AGHIB, D
SAGLIO, G
CAMASCHELLA, C
MAZZA, U
[J]. ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 445 (JUN) : 170 - 176
[3] CLINICAL AND HEMATOLOGICAL EVALUATION OF BETA-THALASSEMIA INTERMEDIA CHARACTERIZED BY UNUSUALLY LOW HB-F AND INCREASED HB-A2-BETA-THALASSEMIA INTERMEDIA-II
GURGEY, A
KAYIN, S
KANSU, E
ALTAY, C
[J]. JOURNAL OF MEDICAL GENETICS, 1985, 22 (03) : 213 - 221
[4] BETA-THALASSEMIA ASSOCIATED WITH INCREASED HB F-PRODUCTION - EVIDENCE FOR THE EXISTENCE OF A HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN (HPFH) DETERMINANT LINKED TO BETA-THALASSEMIA IN A SOUTHERN ITALIAN POPULATION
MARINUCCI, M
GABBIANELLI, M
ZORINI, CO
LAMBERTI, E
PALAZZOLO, A
LANZO, D
[J]. HEMOGLOBIN, 1981, 5 (01) : 1 - 17