Publications - Ā mātou whakaputa
We publish a range of information, from strategies and plans to guidance for clinicians and other health service providers.
Pātiki and Waharua Kōpito patterns
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Position statement regarding newborn screening for muscular dystrophy
The National Screening Unit's position on screening for muscular dystrophy. -
Screening, Diagnosis and Management of Gestational Diabetes in New Zealand: A clinical practice guideline
This clinical guideline gives detailed recommendations for screening and diagnosis of probable undiagnosed type 2 diabetes and gestational diabetes. -
Autosomal recessive inheritance
The information in this resource will help you understand more about autosomal recessive inheritance and answer some of your questions. -
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency and your baby
The information in this resource will help you understand more about medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. -
Cost-effectiveness of Newborn Screening for Severe Combined Immune Deficiency
Report on testing for severe combined immune deficiency (SCID) in New Zealand. -
What is mild hearing loss?
A factsheet for parents whose children have been diagnosed with mild hearing loss. -
What is unilateral hearing loss?
A factsheet for parents whose children have been diagnosed with unilateral hearing loss. -
NCSP Monitoring and Evaluation: Cervical Cancer Case Reviews
Background and external link to the New Zealand Medical Journal article. -
Screening for Severe Combined Immune Deficiency – Literature Review
An economic analysis of the cost-effectiveness of including testing for Severe Combined Immune Deficiency (SCID) in Newborn Metabolic Screening. -
SNOMED Coding for Histology
SNOMED Coding for Histology.