<![CDATA[Department of Health Elibrary Search for 'au:"Estrada, Sylvia"']]>

<![CDATA[Department of Health Elibrary Search for 'au:"Estrada, Sylvia"']]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-search.pl?q=ccl=au%3A%22Estrada%2C%20Sylvia%22&sort_by=relevance&format=rss 12 0 50 Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2742

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2742 Profile of Filipino infants with 21-hydroxylase deficiency congenital adrenal hyperplasia detected by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2939

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2939 Gaucher disease in six Filipino children: a case series / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2972

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=2972 Molecular analysis of the MUT gene in Filipino patients with methylmalonic acidemia / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3009

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3009 Enzyme replacement therapy in Filipino patients with Gaucher disease and Pompe disease / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3010

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3010 Etiology of congenital hypothyroidism among infants screen by the Philippine newborn screening program / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3016

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3016 Galactosemia in three Filipino patients - The importance of newborn screening / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3111

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3111 Detection of maple syrup urine disease on newborn screening second tier testing for phenylketonuria / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3114

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3114 Improved screening efficiency for phenylketonuria using a modified bacterial inhibition assay protocol- Autoclaving the bloodspot / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3115

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3115 Mutations of the steroid 21-hydroxylase gene among Filipino patients with congenital adrenal hyperplasia / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3116

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3116 Mutations of the phenylalanine hydroxylase (PAH) gene in Filipino patients with phenylketonuria / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3118

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3118 Cost-benefit analysis of the newborn screening program of the Philippines / ISBN: https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3280

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]]> https://doh.onstrike.com.ph/cgi-bin/koha/opac-detail.pl?biblionumber=3280