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Galactosemia
Clinical Applications and Implications of Common and Founder Mutations in Indian Subpopulations
Incidence of Inborn Errors of Metabolism by Expanded Newborn
Hereditary Galactokinase Deficiency J
Mild Galactosemia General Overview
Metabolic Liver Diseases Presenting As Acute Liver Failure in Children
Galactosemia, Or Galactose Diabetes
Review Galactokinase: Structure, Function and Role in Type II
The Interrelationships Between Lactose Intolerance and the Modern Dairy Industry: Global Perspectives in Evolutional and Historical Backgrounds
Association of Escherichia Coli Sepsis and Galactosemia in Neonates
Inability to Convert Galactose to Glucose 2 Galactosemia
Fermentation, Fermented Foods and Lactose Intolerance
Classical Galactosemia Information for Parents
Classic Galactosemia and Clinical Variant Galactosemia Synonyms: GALT Deficiency, Galactose-1-Phosphate Uridylyltranserase Deficiency
Glucose 6-Phosphate Dehydrogenase Enzyme Deficiency Among Infants: an Eye Opener to Parents and Would Be Parents”
Galactosemia, Diet and Dairy Products
Point-Of-Care Testing for G6PD Deficiency
Lactose Intolerance: Information for Health Care Providers
Laboratory Diagnosis of Galactosemia: a Technical Standard and Guideline of the American College of Medical Genetics and Genomics (ACMG)
Top View
Newborn Screening ACT Sheet
Hypoallergenic Formulas for Infants
Understanding Galactosemia a Diet Guide
Suggested Follow-Up for Classical Galactosemia Deficient GALT with Normal Total Galactose
Fructose-Induced Hyperuricemia Hereditary Fructose Intolerance Galactosemia Hyperuricemia
The Molecular Basis of Galactosemia - Past, Present and Future
Inborn Errors of Carbohydrate Metabolism
Galactosemia Screening Using Tandem Mass Spectrometry
Development of an Oral Treatment for Galactosemia EDUCATIONAL EVENT
Galactosemia Physician/Health Care Professional Information
Classic Galactosemia General Overview
Carrier Screening Disease & Gene List
NGS-Based Expanded Carrier Screening
Incidence of Inborn Errors of Metabolism in British Columbia, 1969–1996
Dietary Management of Galactosaemia
FRONTIERS in NEPHROLOGY Renal Tubular Acidosis: the Clinical Entity
Galactosemia
Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland by Nina A
Provider Minnesota Newborn Fact Sheetpositive Result: Screening Program Blood Spot Screen Result Notification
Galactokinase, Blood
Galactosemia ACT Sheet
Unit 12 Inborn Errors of Metabolism
Galactosemia, GALT-Related
Galactose-1-Phosphate Uridyl Transferase (GALT) and Galactosemia
Current and Future Treatments for Classic Galactosemia
Galactosaemia Feature Interview with Louise and Is a Member of the Galactosaemia Robertson RD
Diagnosis of Galactosemia by Simple Technique in a Resource-Constraint Country Md
Inborn Errors of Carbohydrate Metabolism
Galactosemia(Galt)
Galactosemia: Towards Pharmacological Chaperones
GALT Deficiency
A Guide to Fluorescent Spot Testing for G6PD Deficiency
Galactosemia: When Is It a Newborn Screening Emergency?☆
Inborn Errors of Metabolism with Hepatopathy Metabolism Defects of Galactose, Fructose, and Tyrosine
Galactose-1- Phosphate Uridylytransferase Sensitive to Product Inhibition by Glucose 1-Phosphate
Galactosemia Galactosemia Galactosemia Newborn Screening (NBS) Panels in All 50 States Include Galactosemia
Invitae Carrier Screening (Continued)
Galactosemia Columbus, OH 43231 Tel: 614/839-3040 PEDIATRIC ENDOCRINOLOGY Fax: 614/839-3041
Galactosemia Information for Physicians and Other Health Care Professionals
Pitfalls in the Diagnosis of Hereditary Fructose Intolerance Alexander Y
A Generalist's Approach to Inborn Errors of Metabolism