Cabello ML - Search Results

1

An asymptomatic variant of maple syrup urine disease without organic aciduria.

Cabello ML, Garcia AM, Dalmau J, Dominguez C, Conde C. Cabello ML, et al. J Inherit Metab Dis. 1994;17(1):115-6. doi: 10.1007/BF00735409. J Inherit Metab Dis. 1994. PMID: 8051917 No abstract available.

2

Improved identification of heterozygotes for phenylketonuria using blood neopterin and biopterin.

Alós T, Bel Y, Cabello ML, Catalá JL, Dalmau J, Ferré J, García AM, Ruiz-Vázquez P. Alós T, et al. Among authors: cabello ml. J Inherit Metab Dis. 1993;16(2):457-64. doi: 10.1007/BF00710298. J Inherit Metab Dis. 1993. PMID: 8412006

3

[Genetic and molecular study of cystinuria in the Valencian community].

Guillén M, Corella D, Cabello ML, García AM, Sáiz C, González JI, Hernández-Yago J. Guillén M, et al. Among authors: cabello ml. Med Clin (Barc). 1999 Sep 25;113(9):321-6. Med Clin (Barc). 1999. PMID: 10562926 Spanish.

4

Reference values of urinary excretion of cystine and dibasic aminoacids: classification of patients with cystinuria in the Valencian Community, Spain.

Guillén M, Corella D, Cabello ML, García AM, Hernández-Yago J. Guillén M, et al. Among authors: cabello ml. Clin Biochem. 1999 Feb;32(1):25-30. doi: 10.1016/s0009-9120(98)00087-3. Clin Biochem. 1999. PMID: 10074888

5

Association between M467T and 114 C-->A variants within the SLC3A1 gene and some phenotypical traits in cystinuria patients from Spain.

Guillén M, Corella D, Cabello ML, García AM, Portolés O, Hernández-Yago J. Guillén M, et al. Among authors: cabello ml. Hum Genet. 2000 Mar;106(3):314-20. doi: 10.1007/s004390051044. Hum Genet. 2000. PMID: 10798361

6

Identification of novel SLC3A1 gene mutations in Spanish cystinuria families and association with clinical phenotypes.

Guillén M, Corella D, Cabello ML, González JI, Sabater A, Chaves JF, Hernández-Yago J. Guillén M, et al. Among authors: cabello ml. Clin Genet. 2005 Mar;67(3):240-51. doi: 10.1111/j.1399-0004.2004.00393.x. Clin Genet. 2005. PMID: 15691362

7

[Sensitivity, specificity and predictive value of the genetic analysis of SLC3A1 gene variants used for the diagnosis of cystinuria among the spanish population].

Guillén M, Corella D, Cabello ML, Saiz C, Hernández-Yago J. Guillén M, et al. Among authors: cabello ml. Rev Clin Esp. 2001 May;201(5):256-9. doi: 10.1016/s0014-2565(01)70812-0. Rev Clin Esp. 2001. PMID: 11458794 Spanish.

8

Genetic and phenotypic aspects of phenylalanine hydroxylase deficiency in Spain: molecular survey by regions.

Desviat LR, Pérez B, Gámez A, Sánchez A, García MJ, Martínez-Pardo M, Marchante C, Bóveda D, Baldellou A, Arena J, Sanjurjo P, Fernández A, Cabello ML, Ugarte M. Desviat LR, et al. Among authors: cabello ml. Eur J Hum Genet. 1999 Apr;7(3):386-92. doi: 10.1038/sj.ejhg.5200312. Eur J Hum Genet. 1999. PMID: 10234516

9

Anonymous testing of newborn infants for HIV antibodies as a basis for estimating prevalence of HIV in childbearing women: the 1991-1994 study in Spain.

Canosa CA, Grady GF, Cabello ML, Comeau AM, Schwerzler ME, Contreras MT, Fraga JM, Gomez de los Terreros I, Pena J. Canosa CA, et al. Among authors: cabello ml. Acta Paediatr Suppl. 1997 Jun;421:67-71. doi: 10.1111/j.1651-2227.1997.tb18324.x. Acta Paediatr Suppl. 1997. PMID: 9240862

10

Separation and identification of sugars and maltodextrines by thin layer chromatography: Application to biological fluids and human milk.

Bosch-Reig F, Marcote MJ, Minana MD, Cabello ML. Bosch-Reig F, et al. Among authors: cabello ml. Talanta. 1992 Nov;39(11):1493-8. doi: 10.1016/0039-9140(92)80131-v. Talanta. 1992. PMID: 18965559

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