Results of search for 'au:"Estrada, Sylvia"' › Department of Health Elibrary catalog

1.

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Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / Ethel M. Estanislao [and three others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000001.

2.

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Profile of Filipino infants with 21-hydroxylase deficiency congenital adrenal hyperplasia detected by the Philippine newborn screening program / Sylvia C. Estrada [and two others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000044.

3.

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Gaucher disease in six Filipino children: a case series / Mary Anne D. Chiong [and three others] by

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Availability: Items available for loan: DOH Central Library (1)Call number: J000067.

4.

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Molecular analysis of the MUT gene in Filipino patients with methylmalonic acidemia / Catherine Lynn T. Sila [and six others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000093.

5.

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Enzyme replacement therapy in Filipino patients with Gaucher disease and Pompe disease / Mary Anne D. Chiong [and four others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000094.

6.

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Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / Ethel M. Estanislao [and four others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000100.

7.

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Galactosemia in three Filipino patients - The importance of newborn screening / John Karl de Dios [and two others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000103.

8.

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Detection of maple syrup urine disease on newborn screening second tier testing for phenylketonuria / Sylvia Capistrano-Estrada, Charity M. Jomento by

Availability: Items available for loan: DOH Central Library (1)Call number: J000106.

9.

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Improved screening efficiency for phenylketonuria using a modified bacterial inhibition assay protocol- Autoclaving the bloodspot / Acta Medica Philippina, 2009 vol 43 (2) pages: 29-31 by

Availability: Items available for loan: DOH Central Library (1)Call number: J000107.

10.

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Mutations of the steroid 21-hydroxylase gene among Filipino patients with congenital adrenal hyperplasia / Eva Maria Cutiongco-de la Paz [and four others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000108.

11.

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Mutations of the phenylalanine hydroxylase (PAH) gene in Filipino patients with phenylketonuria / Catherine Lynn T. Silao [and five others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000109.

12.

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Cost-benefit analysis of the newborn screening program of the Philippines / Carmencita David-Padilla [and six others] by

Availability: Items available for loan: DOH Central Library (1)Call number: J000111.

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