Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany *

An evidence development process for newborn screening

(2010) James M Perrin et al.   GENETICS IN MEDICINE

Newborn Population Screening for Classic Homocystinuria by Determination of Total Homocysteine from Guthrie Cards

(2009) Hongying Gan-Schreier et al.   JOURNAL OF PEDIATRICS

Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years

(2009) B. Wilcken et al.   PEDIATRICS

Guiding Policy Decisions for Genetic Screening: Developing a Systematic and Transparent Approach

(2009) A. Andermann et al.   Public Health Genomics

Revisting wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years

(2008) Anne Andermann   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Developing a national collaborative study system for rare genetic diseases

(2008) Michael S Watson et al.   GENETICS IN MEDICINE

Duarte (DG) galactosemia: A pilot study of biochemical and neurodevelopmental assessment in children detected by newborn screening

(2008) Can Ficicioglu et al.   MOLECULAR GENETICS AND METABOLISM

Clinical research for rare disease: Opportunities, challenges, and solutions

(2008) Robert C. Griggs et al.   MOLECULAR GENETICS AND METABOLISM