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Transaldolase deficiency
Mitochondrial Involvement and Erythronic Acid As a Novel Biomarker in Transaldolase Deficiency Udo F.H
Table S1. Disease Classification and Disease-Reaction Association
Inborn Defects in the Antioxidant Systems of Human Red Blood Cells
Pentose Phosphate Pathway in Health and Disease: from Metabolic
Pentose Phosphate Pathway Biochemistry, Metabolism and Inherited Defects
Diagnose a Broad Range of Metabolic Disorders with a Single Test, Global
SSIEM Classification of Inborn Errors of Metabolism 2011
1 a Clinical Approach to Inherited Metabolic Diseases
Genetic Disorders
Liver Disorders in Inherited Metabolic Disorders
Metabolic Disorders (Children)
Clinical, Biochemical, and Molecular Overview of Transaldolase Deficiency and Evaluation of the Endocrine Function: Update of 34 Patients
Severe Infantile Transaldolase Deficiency
Transaldolase 1 Is Required for Neutrophil Extracellular Trap (NET) Formation
Transaldolase Deficiency a Case Report
The Pentose Phosphate Pathway in Yeasts–More Than a Poor Cousin of Glycolysis
Disorders of the Pentose Phosphate Pathway
Blueprint Genetics Comprehensive Metabolism Panel
Top View
Molecular Characterization of Ribose 5-Phosphate Isomerase Deficiency
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Metabolic Disorders (Laboratory Services)
Report Ribose-5-Phosphate Isomerase Deficiency
Metabolske Sykdommer V02
Novel Neuropathological Features of a Child with an Epileptic Encephalopathy Due to Presumed Polyol Dysmetabolism
1174 Oxidative Stress and Neurodegeneration: the Yeast
Clinical, Biochemical, and Molecular Overview of Transaldolase Deficiency and Evaluation of the Endocrine Function: Update of 34 Patients
Source: State: 12.06.2018 ORPHA68367 10507
Table S4. Disease Prevalence
Individual Genome Sequence Gene List (By Disease)
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Transaldolase Deficiency a Case Report
The Pentose Phosphate Pathway Dynamics in Cancer and Its Dependency on Intracellular Ph
Molecular Genetics and Metabolism 117 (2016) 221–298
A Generalist's Approach to Inborn Errors of Metabolism