Last Posted: May 23, 2019
- A consensus statement on birth defects surveillance, prevention, and care in Latin America and the Caribbean.
Zarante Ignacio et al. Revista panamericana de salud publica = Pan American journal of public health 2019 43e2 - Ethical issues with testing and treatment for Krabbe disease.
Ehmann Paul et al. Developmental medicine and child neurology 2019 May - Health outcomes and services in children with sickle cell trait, sickle cell anemia, and normal hemoglobin.
Reeves Sarah L et al. Blood advances 2019 May 3(10) 1574-1580 - Maximizing the Benefit of Life-Saving Treatments for Pompe Disease, Spinal Muscular Atrophy, and Duchenne Muscular Dystrophy Through Newborn Screening: Essential Steps.
Baker Mei et al. JAMA neurology 2019 May - Implementation of public health genomics in Pakistan.
Riaz Moeen et al. European journal of human genetics : EJHG 2019 May - Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians' current practices.
Yuskiv Nataliya et al. Orphanet journal of rare diseases 2019 14(1) 7 - A report on state-wide implementation of newborn screening for X-linked Adrenoleukodystrophy.
Wiens Katie et al. American journal of medical genetics. Part A 2019 May - Newborn screening for Pompe disease in Japan: report and literature review of mutations in the GAA gene in Japanese and Asian patients.
Momosaki Ken et al. Journal of human genetics 2019 May - Newborn Screening for Congenital Hypothyroidism in India: Let's Just Do It!
Therrell Bradford L et al. Indian pediatrics 2019 Apr 56(4) 275-276 - Association between newborn screening analyte profiles and infant mortality.
Fell Deshayne et al. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2019 May 1-121
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