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Publications by J Abe
Clinical Heterogeneity Among a Three-Generation Japanese Family With D18N TREX1 Mutation for Aicardi-Goutières Syndrome / Familial Chilblain Lupus
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
Tyrosine Phosphorylation of Platelet Derived Growth Factor Beta Receptors in Coronary Artery Lesions: Implications for Vascular Remodelling After Directional Coronary Atherectomy and Unstable Angina Pectoris
Heart
Cardiovascular Medicine
Cardiology
Related publications
Familial Chilblain Lupus Due to a Novel Mutation in TREX1 Associated With Aicardi–Goutie’res Syndrome
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
Aicardi-Goutières Syndrome
Familial Chilblain Lupus Caused by an Activating Mutation in STING
Pediatric Rheumatology
Immunology
Pediatrics
Rheumatology
Allergy
Perinatology
Child Health
Late Diagnosis and Atypical Brain Imaging of Aicardi-Goutières Syndrome: Are We Failing to Diagnose Aicardi-Goutières Syndrome-2?
Developmental Medicine and Child Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Cutting Edge: cGAS Is Required for Lethal Autoimmune Disease in the Trex1-Deficient Mouse Model of Aicardi–Goutières Syndrome
Journal of Immunology
Allergy
Immunology
Three Family Members With Familial Mediterranean Fever Carrying the M694V Mutation Showed Different Clinical Presentations
Internal Medicine
Internal Medicine
Medicine
UBR5Gene Mutation Is Associated With Familial Adult Myoclonic Epilepsy in a Japanese Family
ISRN Neurology
Familial Acromegaly: A Specific Clinical Entity--Further Evidence From the Genetic Study of a Three-Generation Family
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Efficacy of Baricitinib in the Treatment of Chilblains Associated With the Type I Interferonopathy Aicardi-Goutières Syndrome
Arthritis and Rheumatology
Rheumatology
Allergy
Immunology