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Hyperlysinemia
Effect of Propionic Acid on Fatty Acid Oxidation and U Reagenesis
Inherited Metabolic Disease
Metabolomic Analysis Reveals That the Drosophila Gene Lysine Influences Diverse Aspects of Metabolism
Amino Acid Disorders
Table S1. Disease Classification and Disease-Reaction Association
23 Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism
Intestinal Phosphate Transport in Familial ~~~O~Hos~Haternicrickets
Attachment a Rare and Expensive Disease List As of December 27, 2010 ICD-9 Age Disease Guidelines Code Group 042
Familial Hyperlysinemia
Sudden Unexpected Fatal Encephalopathy in Adults with OTC
1 a Clinical Approach to Inherited Metabolic Diseases
12 Disorders of Ornithine, Lysine, and Tryptophan Georg F
The Prognosis of Hyperlysinemia: an Interim Report
Familial Hyperlysinemia with Lysine-Ketoglutarate Reductase Insufficiency
Ketoadipic Aciduria: a Description of a New Metabolic Error in Lysine - Tryptophan Degradation
The Use of Gas Chromatography-Mass Spectrometry for the Diagnosis and Study of Metabolic Disorders I
WES Gene Package Metabolic Disorders.Xlsx
289.Full.Pdf
Top View
Biomarkers Identified in Inborn Errors for Lysine, Arginine, and Ornithine
Catabolism of Carbon Skeletons of Amino Acids and Related Disorders-III
Letter to the Editor: Lysine Intolerance in Methylmalonic Acidemia
How Does Protein Nutrition Affect the Epigenetic Changes in Pig? a Review
Pyruvate Carboxylase Deficiency: Mechanisms, Mimics and Anaplerosis
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
US 2016/0076021 A1 Stojanovic Et Al
Volume 4 (Numbers Followed by Asterisk Refer to Society Abstracts)
Letters to the Editor
Descriptions of Phenotypes
Diagnosed Cases of Rare Diseases at CENTOGENE January 2012 to June 2016
Disorders of Amino Acid Metabolism 1971
Consensus Guidelines for Management of Hyperammonaemia in Paediatric Patients Receiving Continuous Kidney Replacement Therapy
An Inherited Disorder of Ammo Acid Transport1,[34]
Metabolske Sykdommer V02
Urinary Purines and Pyr~Idines in Patients with ~Yper~~One~~ of Various Origins
Supplemental Information
Disorders Affecting Protein Metabolism
Source: State: 12.06.2018 ORPHA68367 10507
Table S4. Disease Prevalence
Six Month Competency for 5600 Techs (New Trainees)
List of Rare Diseases and Synonyms
Differential Diagnosis of (Inherited) Amino Acid Metabolism Or Transport Disorders
The Ophthalmological Manifestations of Various Inborn Errors of Metabolism: a Narrative Review
Genetic Basis of Hyperlysinemia
Pathway Analysis of Metabolic Activities Gabriele Sales 2018-05-21
Hyperlysinemia
Health Care Resource Book
OMIM Mendelian Gene List V2.0
Institute of Anatomy and Biology, Philadelphia, Pennsylvania. Fusion
Nutritional Aspects of Inborn Errors of Metabolism
Amino Acids Support Guide Contents
Recessive Gene List V2.0
Anaplerotic Therapy in Propionic Acidemia