Genetics Issue 3: Volume 43 No. 2

Feature Article

Newborn Screening: Research to Policy
Padilla C, Basilio J, Oliveros Y. [PDF]

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Case Reports

Galactosemia in three Filipino patients - the importance of Newborn Screening
de Dios J, Capistrano-Estrada S, Chiong M. [PDF]

Two Filipino patients with 6-Pyruvoyltetrahydropterin Synthase Deficiency
de Dios J, Chiong M. [PDF]

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Original Articles

Glucose-6-Phosphate Dehydrogenase Deficiency in Filipino Neonates with Jaundice
Silao C, Padilla C, Uy E, et al. [PDF]

Detection of Maple Syrup Urine Disease on Newborn Screening second tier testing for Phenylketonuria
Capistrano-Estrada S, Jomento C. [PDF]

Improved screening efficiency for Phenylketonuria using a Modified Bacterial Inhibition Assay Protocol – Autoclaving the Bloodspot
Carillo C, Tirona J, Capistrano-Estrada S, et al. [PDF]

Mutations of the Steroid 21-Hydroxylase gene among Filipino patients with Congenital Adrenal Hyperplasia
Cutiongco-dela Paz E, Abaya E, Silao C, et al.  [PDF]

Mutations of the Phenylalanine Hydroxylase (PAH) gene in Filipino patients with Phenylketonuria
Silao C, Canson D, Hernandez K, et al. [PDF]

Cost-benefit analysis of a Neonatal Screening Program for Congenital Hypothyroidism in Metro Manila
Dans L, Padilla C for the Newborn Screening Study Group [PDF]

Cost-benefit analysis of the Newborn Screening Program of the Philippines
Padilla C, Dans L, Tamondong M, et al. [PDF]

Models for increasing the Newborn Screening performance of health facilities
Padilla C, Reyes E. [PDF]

A Performance Evaluation and Assessment Scheme (PEAS) for improving the Philippine Newborn Screening Program
Padilla C, Basilio J, Therrell B. [PDF]

Republic Act 9288 or the Newborn Screening Act of 2004 [PDF]

PhilHealth Circular No. 67, s-2009: Clarification on the Newborn Care Package and Normal Spontaneous Delivery and Maternity Care Package [PDF]

Frequently Asked Questions on PhilHealth’s Newborn Care Package [PDF]