Detalhe da pesquisa
1.
Abnormalities in subsets of B and T cells in Mexican patients with inborn errors of propionate metabolism: observations from a single-center case series.
Allergol Immunopathol (Madr)
; 49(1): 101-106, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33528936
2.
Phenylalanine hydroxylase deficiency in Mexico: genotype-phenotype correlations, BH4 responsiveness and evidence of a founder effect.
Clin Genet
; 88(1): 62-7, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24941924
3.
Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference center.
Front Genet
; 13: 993612, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36313470
4.
Thiopurine S-methyltransferase (TPMT) genetic polymorphisms in Mexican newborns.
J Clin Pharm Ther
; 34(6): 703-8, 2009 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-20175804
5.
Low allelic heterogeneity in a sample of Mexican patients with classical galactosaemia.
J Inherit Metab Dis
; 31 Suppl 2: S333-7, 2008 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-18956253
6.
Composition of gut microbiota in obese and normal-weight Mexican school-age children and its association with metabolic traits.
Pediatr Obes
; 13(6): 381-388, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29388394
7.
Abnormalities in subsets of B and T cells in Mexican patients with inborn errors of propionate metabolism: observations from a single-center case series
Allergol. immunopatol
; 49(1): 101-106, ene.-feb. 2021. graf, tab
Artigo
Inglês
| IBECS (Espanha) | ID: ibc-199232
8.
Diagnosis of inborn errors of metabolism.
Arch Med Res
; 31(2): 145-50, 2000.
Artigo
Inglês
| MEDLINE | ID: mdl-10880718
9.
[Pearl S. Buck, Literature Nobel Price, and phenylketonuria: a moving relationship]. / Pearl S. Buck, premio Nobel de Literatura y la fenilcetonuria: una conmovedora relación.
Rev Invest Clin
; 53(6): 573-5, 2001.
Artigo
Espanhol
| MEDLINE | ID: mdl-11921532
10.
[Characterization of inborn errors of intermediary metabolism in mexican patients]. / Caracterización de errores innatos del metabolismo intermediario en pacientes mexicanos.
An Pediatr (Barc)
; 80(5): 310-6, 2014 May.
Artigo
Espanhol
| MEDLINE | ID: mdl-24140120
11.
Tandem mass spectrometry newborn screening for inborn errors of intermediary metabolism: abnormal profile interpretation.
Curr Med Chem
; 19(26): 4511-22, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22934775
12.
Causes of delay in referral of patients with phenylketonuria to a specialized reference centre in Mexico.
J Med Screen
; 18(3): 115-20, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-22045819
13.
Caracterización de errores innatos del metabolismo intermediario en pacientes mexicanos / Characterization of inborn errors of intermediary metabolism in mexican patients
An. pediatr. (2003, Ed. impr.)
; 80(5): 310-316, mayo 2014. tab, graf
Artigo
Espanhol
| IBECS (Espanha) | ID: ibc-122031