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Publications by David Coman
Defective Protein Prenylation in a Spectrum of Patients With Mevalonate Kinase Deficiency
Frontiers in Immunology
Allergy
Immunology
International Clinical Guidelines for the Management of Phosphomannomutase 2-Congenital Disorders of Glycosylation: Diagnosis, Treatment and Follow Up
Journal of Inherited Metabolic Disease
Genetics
Related publications
Mevalonate Kinase Deficiency: Current Perspectives
The Application of Clinical Genetics
Genetics
PW03-021 - HSCT in Mevalonate Kinase Deficiency
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
Identification of an Active Site Alanine in Mevalonate Kinase Through Characterization of a Novel Mutation in Mevalonate Kinase Deficiency
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
PW02-020 - Colitis Revealing Mevalonate Kinase Deficiency
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
THU0547 Characterization of a Group of 12 Patients With Mevalonate Kinase Deficiency: Symptoms and Treatment With Il-1 Inhibitors
Inhibition of Mevalonate Pathway Prevents Adipocyte Browning in Mice and Men by Affecting Protein Prenylation
Cell Metabolism
Cell Biology
Molecular Biology
Physiology
Multi-Omics Analyses unveilSTAT1as a Potential Modifier Gene in Mevalonate Kinase Deficiency
Annals of the Rheumatic Diseases
Immunology
Molecular Biology
Biochemistry
Rheumatology
Allergy
Genetics
Regulatory Adaptation of Isoprenoid Biosynthesis and the LDL Receptor Pathway in Fibroblasts From Patients With Mevalonate Kinase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Natural Isoprenoids Are Able to Reduce Inflammation in a Mouse Model of Mevalonate Kinase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology