Detalhe da pesquisa
1.
Hyperphenylalaninemia in the Philippines.
Southeast Asian J Trop Med Public Health
; 34 Suppl 3: 182-4, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-15906731
2.
6-pyruvoyl tetrahydropterin synthase deficiency: a case report.
Southeast Asian J Trop Med Public Health
; 34 Suppl 3: 186-8, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-15906733
3.
Initial versus confirmatory thyroid stimulating hormone (TSH) levels: is there a correlation?
Southeast Asian J Trop Med Public Health
; 34 Suppl 3: 154-7, 2003.
Artigo
Inglês
| MEDLINE | ID: mdl-15906724
4.
Classical hemocystinuria in two Filipino patients
Acta Medica Philippina
; : 81-83, 2011.
Artigo
Inglês
| WPRIM | ID: wpr-631858
5.
Early diagnosis and specialist care in the management of congenital hypothyroidism
Acta Medica Philippina
; : 40-45, 2011.
Artigo
Inglês
| WPRIM | ID: wpr-631847
6.
Detection of maple syrup urine disease on newborn screening second tier testing for phenylketonuria
Acta Medica Philippina
; : 26-28, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633838
7.
Improved screening efficiency for phenylketonuria using a modified bacterial inhibition assay protocol- Autoclaving the bloodspot
Acta Medica Philippina
; : 29-31, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633839
8.
Galactosemia in three Filipino patients - The importance of newborn screening
Acta Medica Philippina
; : 15-17, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633835
9.
Cost-benefit analysis of the newborn screening program of the Philippines
Acta Medica Philippina
; : 46-52, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633843
10.
Mutations of the phenylalanine hydroxylase (PAH) gene in Filipino patients with phenylketonuria
Acta Medica Philippina
; : 36-39, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633841
11.
Mutations of the steroid 21-hydroxylase gene among Filipino patients with congenital adrenal hyperplasia
Acta Medica Philippina
; : 32-35, 2009.
Artigo
Inglês
| WPRIM | ID: wpr-633840