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Publications by Yasutsugu Chinen
A New Mutation Found in Newborn Screening for Fabry Disease Evaluated by Plasma Globotriaosylsphingosine Levels
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Related publications
Newborn Screening for Fabry Disease in Japan: Prevalence and Genotypes of Fabry Disease in a Pilot Study
Journal of Human Genetics
Genetics
High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening*
American Journal of Human Genetics
Genetics
Vascular Aspects of Fabry Disease in Relation to Clinical Manifestations and Elevations in Plasma Globotriaosylsphingosine * Novelty and Significance
Hypertension
Internal Medicine
Screening for Fabry Disease in Patients With Chronic Kidney Disease: Limitations of Plasma -Galactosidase Assay as a Screening Test
Clinical Journal of the American Society of Nephrology
Epidemiology
Nephrology
Critical Care
Transplantation
Intensive Care Medicine
Screening, Diagnosis and Treatment of Fabry Disease
Clinical pharmacology and therapy
Newborn Screening for Sickle Cell Disease in St. Vincent and the Grenadines: Results of a Pilot Newborn Screening Program
Global Pediatric Health
Child Health
Pediatrics
Perinatology
Update: Newborn Screening for Sickle Cell Disease—California, Illinois, and New York, 1998
JAMA - Journal of the American Medical Association
Medicine
Mass Screening of the Newborn for Metabolic Disease.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Cognitive Impairment and Fabry Disease: A Case Report With Mutation S126G
Neuropsychological Trends
Molecular Neuroscience
Physiological Psychology
Neuropsychology
Cellular