Pujades MA - Search Results

1

[Molecular analysis of glucose-6-dehydrogenase deficiency in Spain].

Vives Corrons JL, Zarza R, Aymerich JM, Boixadera J, Carrera A, Colomer D, Corbella M, Castro M, Crespo JM, Del Arco A, Erkiaga S, Font L, González I, Juncá J, Lausin A, Manrubia E, Martín Núñez G, Murga MJ, Oliva E, Pérez de Mendiguren B, Pujades MA, Remacha A, Rovira A, Villegas A. Vives Corrons JL, et al. Among authors: pujades ma. Sangre (Barc). 1997 Oct;42(5):391-8. Sangre (Barc). 1997. PMID: 9424740 Spanish.

2

Molecular genetics of the glucose-6-phosphate dehydrogenase (G6PD) Mediterranean variant and description of a new G6PD mutant, G6PD Andalus1361A.

Vives-Corrons JL, Kuhl W, Pujades MA, Beutler E. Vives-Corrons JL, et al. Among authors: pujades ma. Am J Hum Genet. 1990 Sep;47(3):575-9. Am J Hum Genet. 1990. PMID: 2393028 Free PMC article.

3

Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum.

Vives-Corrons JL, Pujades MA, Petit J, Colomer D, Corbella M, Aguilar i Bascompte JL, Merino A. Vives-Corrons JL, et al. Among authors: pujades ma. Hum Genet. 1989 Jan;81(2):161-4. doi: 10.1007/BF00293894. Hum Genet. 1989. PMID: 2912886

4

[Cytochemical study of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) and its usefulness in the detection of a heterozygotic deficiency of G6PD].

Vives Corrons JL, Merino A, Pujades MA. Vives Corrons JL, et al. Among authors: pujades ma. Sangre (Barc). 1986;31(4):467-75. Sangre (Barc). 1986. PMID: 3787415 Spanish. No abstract available.

5

[Molecular aspects of an asymptomatic deficit of glucose-6-phosphate dehydrogenase].

Vives Corrons JL, Pujades MA. Vives Corrons JL, et al. Among authors: pujades ma. Sangre (Barc). 1984;29(6):1030-6. Sangre (Barc). 1984. PMID: 6533835 Spanish. No abstract available.

6

Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD gene.

Rovira A, Vulliamy T, Pujades MA, Luzzatto L, Corrons JL. Rovira A, et al. Among authors: pujades ma. Br J Haematol. 1995 Sep;91(1):66-71. doi: 10.1111/j.1365-2141.1995.tb05246.x. Br J Haematol. 1995. PMID: 7577654

7

[Identification of molecular variants of the enzyme glucose-6-phosphate dehydrogenase by the polymerase chain reaction technique].

Rovira A, Vives Corrons JL, Estrada M, Gutiérrez A, Pujades MA, Colomer D, Corbella M, Aymerich M. Rovira A, et al. Among authors: pujades ma. Med Clin (Barc). 1994 Mar 5;102(8):281-4. Med Clin (Barc). 1994. PMID: 8170224 Spanish.

8

[Chronic non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency in a Costa Rican family carrying hemoglobin C disease].

Chaves M, Vives-Corrons JL, Sáenz GF, Pujades MA, Briceño J, Colomer D. Chaves M, et al. Among authors: pujades ma. Sangre (Barc). 1990 Apr;35(2):128-33. Sangre (Barc). 1990. PMID: 2363093 Spanish.

9

A sensitive cytochemical staining method for glucose-6-phosphate dehydrogenase (G6PD) activity in individual erythrocytes.

Vives Corrons JL, Merino A, Pujades MA. Vives Corrons JL, et al. Among authors: pujades ma. Br J Haematol. 1986 Jun;63(2):400-2. doi: 10.1111/j.1365-2141.1986.tb05569.x. Br J Haematol. 1986. PMID: 2424489 No abstract available.

10

Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.

Vives-Corrons JL, Pujades MA, Miguel-García A, Miguel-Sosa A, Cambiazzo S. Vives-Corrons JL, et al. Among authors: pujades ma. Blood. 1992 Sep 15;80(6):1582-5. Blood. 1992. PMID: 1520881 Free article.

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