Suchergebnisse - "Sugiura, K"

PubPharm (645)

1

Time-deterministic cryo-optical microscopy

enthalten in: bioRxiv.org | 2023

von Yamanaka, M. | Tsuji, K. | Kumamoto, Y. | +17

2

Cutaneous ischemia-reperfusion injury is exacerbated by IL-36 receptor antagonist deficiency

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2022

von Tanaka, Y. | Iwata, Y. | Saito, K. | +5

CommentIn: J Eur Acad Dermatol Venereol. 2022 Feb;36(2):163. - PMID 35037306

3

Cutaneous ischemia‐reperfusion injury is exacerbated by IL‐36 receptor antagonist deficiency

enthalten in: Journal of the European Academy of Dermatology and Venereology | 2022

von Tanaka, Y. | Iwata, Y. | Saito, K. | +5

4

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti-BP230 autoantibodies only

enthalten in: The British journal of dermatology | 2020

von Taki, T. | Takeichi, T. | Kono, M. | +5

5

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only

enthalten in: British Journal of Dermatology | 2020

von Taki, T. | Takeichi, T. | Kono, M. | +5

6

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT

enthalten in: The British journal of dermatology | 2018

von Takeichi, T. | Sugiura, K. | Tanahashi, K. | +3

7

Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

enthalten in: Scientific reports | 2018

von Taki, T. | Takeichi, T. | Sugiura, K. | +1

8

Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children

enthalten in: The British journal of dermatology | 2018

von Kono, M. | Akiyama, M. | Inoue, Y. | +10

9

Quantitative risk assessment of the introduction of rabies into Japan through the importation of dogs and cats worldwide - ADDENDUM

enthalten in: Epidemiology and infection | 2018

von Kwan, N. | Sugiura, K. | Hosoi, Y. | +2

ErratumFor: Epidemiol Infect. 2017 Apr;145(6):1168-1182. - PMID 28095930

10

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient

enthalten in: The British journal of dermatology | 2018

von Takeichi, T. | Katayama, C. | Tanaka, T. | +6

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