Kenji Nakagawa
Kyoto, 6068597, Japan
Last Updated: 09/26/2026
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Found 8 publications
A case of novel NFKB2 variant with hypertensive emergency and nephrotic syndrome leading to CKD 5D.
Journal: Pediatric nephrology (Berlin, Germany)
Published: December 16, 2023
Cryopyrin-associated Periodic Syndromes in Italian Patients: Evaluation of the Rate of Somatic NLRP3 Mosaicism and Phenotypic Characterization.
Journal: The Journal of rheumatology
Published: June 30, 2017
Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq.
Journal: Biochemistry and biophysics reports
Published: July 14, 2016
Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children.
Journal: Clinical and experimental rheumatology
Published: August 10, 2015
Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function.
Journal: European journal of human genetics : EJHG
Published: March 02, 2015
Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis.
Journal: British journal of haematology
Published: January 05, 2015
Aicardi-Goutières syndrome is caused by IFIH1 mutations.
Journal: American journal of human genetics
Published: March 01, 2014
Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes.
Journal: Annals of the rheumatic diseases
Published: December 12, 2013
Showing 1-8 of 8
Last Updated: 09/26/2026