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Results: 1-15 |
Results: 15
TRADE-OFFS IN PRENATAL DETECTION OF DOWN-SYNDROME
Authors: SERRAPRAT M GALLO P JOVELL AJ AYMERICH M ESTRADA MD
Citation: M. Serraprat et al., TRADE-OFFS IN PRENATAL DETECTION OF DOWN-SYNDROME, American journal of public health, 88(4), 1998, pp. 551-557
2 NEW MUTATIONS OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) GENE ASSOCIATED WITH HEMOLYTIC-ANEMIA - CLINICAL, BIOCHEMICAL AND MOLECULARRELATIONSHIPS
Authors: ZARZA R PUJADES A ROVIRA A SAAVEDRA R FERNANDEZ J AYMERICH M CORRONS JLV
Citation: R. Zarza et al., 2 NEW MUTATIONS OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) GENE ASSOCIATED WITH HEMOLYTIC-ANEMIA - CLINICAL, BIOCHEMICAL AND MOLECULARRELATIONSHIPS, British Journal of Haematology, 98(3), 1997, pp. 578-582
FIRST DESCRIPTION OF A FRAMESHIFT MUTATION IN THE ALPHA(1)-GLOBIN GENE ASSOCIATED WITH ALPHA-THALASSEMIA
Authors: AYALA S COLOMER D AYMERICH M ABELLA E CORRONS JLV
Citation: S. Ayala et al., FIRST DESCRIPTION OF A FRAMESHIFT MUTATION IN THE ALPHA(1)-GLOBIN GENE ASSOCIATED WITH ALPHA-THALASSEMIA, British Journal of Haematology, 98(1), 1997, pp. 47-50
CONGENITAL 6-PHOSPHOGLUCONATE DEHYDROGENASE (6PGD) DEFICIENCY ASSOCIATED WITH CHRONIC HEMOLYTIC-ANEMIA IN A SPANISH FAMILY
Authors: CORRONS JLV COLOMER D PUJADES A ROVIRA A AYMERICH M MERINO A BASCOMPTE JLAI
Citation: Jlv. Corrons et al., CONGENITAL 6-PHOSPHOGLUCONATE DEHYDROGENASE (6PGD) DEFICIENCY ASSOCIATED WITH CHRONIC HEMOLYTIC-ANEMIA IN A SPANISH FAMILY, American journal of hematology, 53(4), 1996, pp. 221-227
NONDELETIONAL ALPHA-THALASSEMIA - FIRST DESCRIPTION OF ALPHA(HPH)ALPHA AND ALPHA(NCO)ALPHA MUTATIONS IN A SPANISH POPULATION
Authors: AYALA S COLOMER D AYMERICH M PUJADES A VIVESCORRONS JL
Citation: S. Ayala et al., NONDELETIONAL ALPHA-THALASSEMIA - FIRST DESCRIPTION OF ALPHA(HPH)ALPHA AND ALPHA(NCO)ALPHA MUTATIONS IN A SPANISH POPULATION, American journal of hematology, 52(3), 1996, pp. 144-149
HEMOGLOBIN LLEIDA - A NEW ALPHA(2)-GLOBIN VARIANT(12 BP DELETION) WITH MILD THALASSEMIC PHENOTYPE
Authors: AYALA S COLOMER D PUJADES A AYMERICH M CORRONS JLV
Citation: S. Ayala et al., HEMOGLOBIN LLEIDA - A NEW ALPHA(2)-GLOBIN VARIANT(12 BP DELETION) WITH MILD THALASSEMIC PHENOTYPE, British Journal of Haematology, 94(4), 1996, pp. 639-644
MOLECULAR-GENETICS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD)DEFICIENCY IN SPAIN
Authors: CORRONS JLV AYMERICH M CARRERA A COLOMER D FERNANDEZ MJM DEMENDIGUEREN BP PUJADES MA REMACHA A ROVIRA A SAAVEDRA R ZARZA R
Citation: Jlv. Corrons et al., MOLECULAR-GENETICS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD)DEFICIENCY IN SPAIN, Blood, 88(10), 1996, pp. 2756-2756
ALPHA-THALASSEMIA IN SPAIN - FIRST DESCRIPTION OF NON DELETIONAL MUTATIONS AND OF A NEW GLOBIN VARIANT
Authors: CORRONS JLV AYALA S COLOMER D PUJADES MA AYMERICH M
Citation: Jlv. Corrons et al., ALPHA-THALASSEMIA IN SPAIN - FIRST DESCRIPTION OF NON DELETIONAL MUTATIONS AND OF A NEW GLOBIN VARIANT, Blood, 88(10), 1996, pp. 2837-2837
HIGHER INCIDENCE OF ISOLATED OR COMBINED DEFICIENCY OF BAND-3 AND OR BAND-4.2 IN HEREDITARY SPHEROCYTOSIS (HS)/
Authors: AYALA S BESSON I AYMERICH M BERGA L CORRONS JLV
Citation: S. Ayala et al., HIGHER INCIDENCE OF ISOLATED OR COMBINED DEFICIENCY OF BAND-3 AND OR BAND-4.2 IN HEREDITARY SPHEROCYTOSIS (HS)/, International journal of hematology, 62(1), 1995, pp. 53-54
ABNORMALITIES OF RED-BLOOD-CELL MEMBRANE- PROTEINS IN HEREDITARY SPHEROCYTOSIS AND THEIR RELATIONSHIP WITH CLINICAL AND BIOLOGICAL ASPECTS OF THE DISEASE
Authors: AYALA S BESSON I AYMERICH M BERGA L CORRONS JLV
Citation: S. Ayala et al., ABNORMALITIES OF RED-BLOOD-CELL MEMBRANE- PROTEINS IN HEREDITARY SPHEROCYTOSIS AND THEIR RELATIONSHIP WITH CLINICAL AND BIOLOGICAL ASPECTS OF THE DISEASE, Medicina Clinica, 105(2), 1995, pp. 45-49
HEREDITARY XEROCYTOSIS - A REPORT OF 6 UNRELATED SPANISH FAMILIES WITH LEAKY RED-CELL SYNDROME AND INCREASED HEAT-STABILITY OF THE ERYTHROCYTE-MEMBRANE
Authors: CORRONS JLV BESSON I AYMERICH M AYALA S ALLOISIO N DELAUNAY J GONZALEZ I MANRUBIA E
Citation: Jlv. Corrons et al., HEREDITARY XEROCYTOSIS - A REPORT OF 6 UNRELATED SPANISH FAMILIES WITH LEAKY RED-CELL SYNDROME AND INCREASED HEAT-STABILITY OF THE ERYTHROCYTE-MEMBRANE, British Journal of Haematology, 90(4), 1995, pp. 817-822
THE IDENTIFICATION OF MOLECULAR VARIANTS OF THE ENZYME GLUCOSE-6-PHOSPHATE-DEHYDROGENASE BY THE POLYMERASE CHAIN-REACTION TECHNIQUE
Authors: ROVIRA A CORRONS JLV ESTRADA M GUTIERREZ A PUJADES MA COLOMER D CORBELLA M AYMERICH M
Citation: A. Rovira et al., THE IDENTIFICATION OF MOLECULAR VARIANTS OF THE ENZYME GLUCOSE-6-PHOSPHATE-DEHYDROGENASE BY THE POLYMERASE CHAIN-REACTION TECHNIQUE, Medicina Clinica, 102(8), 1994, pp. 281-284
THE DIAGNOSIS OF PAROXYSMAL-NOCTURNAL HEM OGLOBINURIA BY CYTOFLUOROMETRIC ANALYSIS OF MOLECULES BOUND TO THE MEMBRANE BY GLYCOSYL-PHOSPHATIDYLINOSITOL GROUPS
Authors: VILLAMOR N MARIN P AYMERICH M ARRIOLS R ROVIRA M BOSCH F VILELLA R ROZMAN C VIVESCORRONS JL
Citation: N. Villamor et al., THE DIAGNOSIS OF PAROXYSMAL-NOCTURNAL HEM OGLOBINURIA BY CYTOFLUOROMETRIC ANALYSIS OF MOLECULES BOUND TO THE MEMBRANE BY GLYCOSYL-PHOSPHATIDYLINOSITOL GROUPS, Medicina Clinica, 102(13), 1994, pp. 481-484
ELLIPTOPOIKILOCYTOSIS ASSOCIATED WITH THE ALPHA-469 HIS -] PRO MUTATION IN SPECTRIN BARCELONA (ALPHA-I 50-46B)/
Authors: DALLAVENEZIA N ALLOISIO N FORISSIER A DENOROY L AYMERICH M VIVESCORRONS JL BESALDUCH J BESSON I DELAUNAY J
Citation: N. Dallavenezia et al., ELLIPTOPOIKILOCYTOSIS ASSOCIATED WITH THE ALPHA-469 HIS -] PRO MUTATION IN SPECTRIN BARCELONA (ALPHA-I 50-46B)/, Blood, 82(5), 1993, pp. 1661-1665
CONGENITAL XEROCYTOSIS - CLINICAL, HEMATOLOGICAL AND GENETIC-STUDIES OF 7 UNRELATED FAMILIES (12 CASES) FOUND IN SPAIN
Authors: VIVESCORRONS JL BESSON I GONZALEZ I AYALA S MANRUBIA E AYMERICH M
Citation: Jl. Vivescorrons et al., CONGENITAL XEROCYTOSIS - CLINICAL, HEMATOLOGICAL AND GENETIC-STUDIES OF 7 UNRELATED FAMILIES (12 CASES) FOUND IN SPAIN, Blood, 82(10), 1993, pp. 10000088-10000088
Risultati: 1-15 |