about
Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1Progressive neurologic disorder: Initial manifestation of hemophagocytic lymphohistiocytosis.Paediatric Behçet's disease: a UK tertiary centre experienceEarly-Onset Juvenile SLE Associated With a Novel Mutation in Protein Kinase C δ.Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis.Effect of allergic rhinitis and asthma on the quality of life in young Thai adolescents.Cutaneous Vasculitis and Recurrent Infection Caused by Deficiency in Complement Factor I.Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases.Monogenic polyarteritis nodosa caused by ADA2 Deficiency: the GOSH experience.Severe autoinflammatory disease caused by mutation in a gene controlling actin cytoskeletal dynamics and cure with allogeneic haematopoetic stem cell transplantation.Stimulator of interferon genes-associated vasculitis of infancyAdenosine Deaminase Two and Immunoglobulin M Accurately Differentiate Adult Sneddon's Syndrome of Unknown Cause
P50
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P50
description
researcher ORCID ID = 0000-0003-3196-4657
@en
wetenschapper
@nl
name
Sira Nanthapisal
@ast
Sira Nanthapisal
@en
Sira Nanthapisal
@es
Sira Nanthapisal
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type
label
Sira Nanthapisal
@ast
Sira Nanthapisal
@en
Sira Nanthapisal
@es
Sira Nanthapisal
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prefLabel
Sira Nanthapisal
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Sira Nanthapisal
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Sira Nanthapisal
@es
Sira Nanthapisal
@nl
P1153
55293676600
P31
P496
0000-0003-3196-4657