Nobuo Kanazawa
Biographic Data
| ID | 8255483 |
|---|---|
| NAME | Nobuo Kanazawa |
| GIVEN NAMES | Nobuo |
| FAMILY NAME | Kanazawa |
| SIGNATURE | KANAZAWA N |
| AFFILIATIONS | Hyogo Medical University |
| ORCID | 0000-0003-3000-9711 |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2021 |
| LATEST PUBLICATION YEAR | 2022 |
| H-INDEX | 0 |
Dupilumab Improves Pruritus in Netherton Syndrome
The patient was a 26-year-old male. He had red and scaling skin of the entire body since birth, as well as an elevated level of serum IgE. Genetic testing revealed a mutation in the SPINK5 gene, which had confirmed the diagnosis with Netherton syndrome. He has had significant pruritis since birth, and subsequently had symptoms of sleeping disorders and concentration difficulty throughout the day. Since treatment with various antihistamines were n…
NOD2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination
We describe a patient who developed multiple granulomatous skin lesions after Bacille de Calmette et Guérin (BCG) vaccination without significant effect by topical corticosteroid, followed by painless cystic tumors on the bilateral knees and hands and inflammatory changes on ophthalmologic examination. A functional mutation in NOD 2 was detected by a genetic analysis, and he was diagnosed as sporadic Blau syndrome. Since NOD 2 acts as a sensor fo…
Sustained Surface Icam-1 Expression and Transient PDGF-B Production by Phorbol Myristate Acetate-Activated THP-1 Cells Harboring Blau Syndrome-Associated NOD2 Mutations
Sustained surface ICAM-1 expression and transient PDGF-B production by newly differentiating macrophages harboring mutant NOD2 might play a role in granuloma formation in Blau syndrome
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NOD2 Mutation-Associated Case with Blau Syndrome Triggered by BCG Vaccination
We describe a patient who developed multiple granulomatous skin lesions after Bacille de Calmette et Guérin (BCG) vaccination without significant effect by topical corticosteroid, followed by painless cystic tumors on the bilateral knees and hands and inflammatory changes on ophthalmologic examination. A functional mutation in NOD 2 was detected by a genetic analysis, and he was diagnosed as sporadic Blau syndrome. Since NOD 2 acts as a sensor fo…
Sustained Surface Icam-1 Expression and Transient PDGF-B Production by Phorbol Myristate Acetate-Activated THP-1 Cells Harboring Blau Syndrome-Associated NOD2 Mutations
Sustained surface ICAM-1 expression and transient PDGF-B production by newly differentiating macrophages harboring mutant NOD2 might play a role in granuloma formation in Blau syndrome
Dupilumab Improves Pruritus in Netherton Syndrome
The patient was a 26-year-old male. He had red and scaling skin of the entire body since birth, as well as an elevated level of serum IgE. Genetic testing revealed a mutation in the SPINK5 gene, which had confirmed the diagnosis with Netherton syndrome. He has had significant pruritis since birth, and subsequently had symptoms of sleeping disorders and concentration difficulty throughout the day. Since treatment with various antihistamines were n…
Autoimmune and Inflammatory Disorders (2 works) · Biology (2 works) · Dermatology (2 works) · Genetics (2 works) · Immune system (2 works) · Immunology (2 works) · Medicine (2 works) · NOD2 (2 works) · Sarcoidosis and Beryllium Toxicity Research (2 works) · Adverse effect (1 work)