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Argininosuccinic acid
Endogenous Metabolites: JHU NIMH Center Page 1
Argininosuccinate Lyase Deficiency
The First Neonatal Case of Neonatal Argininosuccinic Aciduria in Korea
Molecular Docking Studies of Natural Compounds of Naringin on Enzymes Involved in the Urea Cycle Pathway in Hyperammonemia
Quantitative Amino Acids Analysis for the Diagnosis and Follow up of Inborn Errors of Metabolism
Enzymologic and Metabolic Studies in Two Families Affected by Argininosuccinic Aciduria
Argininosuccinic Aciduria Exclude Antecedent Rheumatic Carditis
The Molecular Basis and Pathology of Phenotypic Variability in Urea Cycle Disorders
Mass Spectrometry – a Powerful Tool for Metabolomics Sandy Nargund Manager, MS & Chromato Shimadzu [Asia-Pacific] Pte Ltd
Next-Generation Metabolic Screening: Targeted and Untargeted Metabolomics for the Diagnosis of Inborn Errors of Metabolism in Individual Patients
The Metabolism of L-Arginine and Its Significance for the Biosynthesis Of
Supplemental Information Table S1, Related to Figure 1. Summary Characteristics of the Leigh Syndrome Patient Derived Fibroblast
Wo 2012/058621 A2
Reliability of Neonatal Screening Results
A Mouse Model of Argininosuccinic Aciduria: Biochemical Characterization
Irritability, Poor Feeding and Respiratory Alkalosis in Newborns: Think About Metabolic Emergencies
Argininosuccinic Acidemia Information for Health Professionals
Neonatal Onset Argininosuccinic Acidemia in a Set of Twins: a Case Report
Top View
A Gene Therapy Approach for Argininosuccinic Aciduria
Argininosuccinic Aciduria an Inborn Error of Amino Acid Metabolism
Alterations in Serum-Free Amino Acid Profiles in Childhood Asthma
20 Disorders of the Urea Cycle and Related Enzymes
Urea Cycle Related Amino Acids Measured in Dried Bloodspots Enable Long-Term in Vivo Monitoring and Therapeutic Adjustment
Questions Health Care Providers Frequently Ask
Bacterial Metabolism of Arginine Mitchell Korzenovsky Iowa State College
Nitrogen Fixation Urea Cycle
Argininosuccinate Lyase Deficiency
MYC Regulates Ribosome Biogenesis and Mitochondrial Gene Expression
Hyperammonaemia: a Deficiency of Liver Ornithine Transcarbamylase Occurrence in Mother and Child B
Newborn Screening ACT Sheet [Increased Citrulline]
Citrullinemia/Argininosuccinic Aciduria – Amino Acid Disorders
UCD GUIDELINE – 1St REVISION 2018
Amino Acid Profiles of Serum and Urine in Search for Prostate Cancer Biomarkers: a Pilot Study Paweł Dereziński1, Agnieszka Klupczynska1, Wojciech Sawicki2, Jerzy A
Protein and Amino Acids
Argininosuccinic Aciduria: Identification and Reactions of The
Study Protocol and Statistical Analysis Plan