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ACTA MEDICA PHILIPPINA
Vol 54 No 4 (2020): Genetics Issue 6
ORIGINAL ARTICLE
Clinical, Biochemical, and Radiologic Characteristics of Filipino Patients with Glutaric Aciduria Type 1
Clinical and Biochemical Profiles of Filipino Patients with Distal Urea Cycle Disorders Detected by Abnormal Expanded Newborn Screening
Gaps in the Newborn Screening Process: Using Maple Syrup Urine Disease as a Case
Filipino Midwives’ Knowledge, Self-perceived Role and Experiences in Educating Parents of Families with Newborns who are Confirmed Cases of Glucose 6 Phosphate Dehydrogenase Deficiency
Vol 51 No 3 (2017)
ORIGINAL ARTICLE
Clinical, Biochemical and Molecular Profile of Variant Galactosemia in Children Detected by National Newborn Screening: A Pilot Study
Parent-Child Communication about Congenital Adrenal Hyperplasia: Filipino Mothers’ Experience
Volume 47 Number 1 Jan-Mar 2013
Volume 46 Number 4 Oct-Dec 2012
ORIGINAL ARTICLE
Enhancing Case Detection of Selected Inherited Disorders through Expanded Newborn Screening in the Philippines
Volume 45 Number 4 Oct-Dec 2011
FEATURE ARTICLE
A Master of Science in Genetic Counseling Program in the Philippines
ORIGINAL ARTICLE
Early Diagnosis and Specialist Care in the Management of Congenital Hypothyroidism
Characterization of Mutations and Polymorphisms in the G6PD Gene among Filipino Newborns with Glucose-6-Phospate Dehydrogenase Deficiency
Volume 43 Number 2 2009
FEATURE ARTICLE
Newborn Screening: Research to Policy
CASE REPORTS
Galactosemia in Three Filipino Patients - The Importance of Newborn Screening
Two Filipino Patients with 6-Pyruvoyltetrahydropterin Synthase Deficiency
ORIGINAL ARTICLES
Glucose-6-Phosphate Dehydrogenase Deficiency in Filipino Neonates with Jaundice
Incidental Detection of Maple Syrup Urine Disease on Newborn Screening Second Tier Testing for Phenylketonuria
Improved Screening Efficiency for Phenylketonuria using a Modified Bacterial Inhibition Assay Protocol - Autoclaving the Bloodspot
Mutations of the Steroid 21-Hydroxylase Gene among Filipino Patients with Congenital Adrenal Hyperplasia
Mutations of the Phenylalanine Hydroxylase (PAH) Gene in Filipino Patients with Phenylketonuria
Cost-Benefit Analysis of a Neonatal Screening Program for Congenital Hypothyroidism in Metro Manila
Cost-Benefit Analysis of the Newborn Screening Program of the Philippines
Models for Increasing the Newborn Screening Performance of Health Facilities
A Performance Evaluation and Assessment Scheme (PEAS) for Improving the Philippine Newborn Screening Program
PHILIPPINE JOURNAL OF HEALTH RESEARCH AND DEVELOPMENT
Vol 22, No 3 (2018)
Facilitating Factors and Barriers to Newborn Screening Uptake in the Cordillera Administrative Region and Region V
PHILIPPINE JOURNAL OF SCIENCCE
Vol. 150 No. 2, April 2021
Common Alpha Globin Genes (HBA1 and HBA2) Mutations in Filipino Patients with Alpha Thalassemia
INTERNATIONAL JOURNAL OF NEONATAL SCREENING
2022; 8(1): 8
Successful Implementation of Expanded Newborn Screening in the Philippines Using Tandem Mass Spectrometry
2021, 7(2): 30
Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines
2020, 6(4): 95
Philippine Performance Evaluation and Assessment Scheme (PPEAS): Experiences in Newborn Screening System Quality Improvement
MOLECULAR GENETICS AND METABOLISM REPORTS
27 (2021) 100745
Pregnancy in an adolescent with maple syrup urine disease: Case report
BMJ JOURNALS
BMJ Case Reports CP 2021;14:e242689
Maple syrup urine disease associated with nephrotic syndrome in a Filipino child
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