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Items: 1 to 20 of 90

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1.

A novel WRN mutation identified in a patient with Werner syndrome and acute generalized exanthematous pustulosis.

Kawai T, Hayashi R, Hama N, Shinkuma S, Fujimoto A, Shimomura Y, Abe R.

Eur J Dermatol. 2018 Jun 28. doi: 10.1684/ejd.2018.3354. [Epub ahead of print] No abstract available.

PMID:
29952303
2.

The development of induced pluripotent stem cell-derived mesenchymal stem/stromal cells from normal human and RDEB epidermal keratinocytes.

Nakayama C, Fujita Y, Matsumura W, Ujiie I, Takashima S, Shinkuma S, Nomura T, Abe R, Shimizu H.

J Dermatol Sci. 2018 Jun 18. pii: S0923-1811(18)30247-0. doi: 10.1016/j.jdermsci.2018.06.004. [Epub ahead of print]

PMID:
29933899
3.

CADM1 is a diagnostic marker in early-stage mycosis fungoides: Multicenter study of 58 cases.

Yuki A, Shinkuma S, Hayashi R, Fujikawa H, Kato T, Homma E, Hamade Y, Onodera O, Matsuoka M, Shimizu H, Iwata H, Abe R.

J Am Acad Dermatol. 2018 Jun 18. pii: S0190-9622(18)32147-9. doi: 10.1016/j.jaad.2018.06.025. [Epub ahead of print]

PMID:
29928911
4.

Two cases of hypohidrotic ectodermal dysplasia caused by novel deletion mutations in the EDA gene.

Nakajima M, Hayashi R, Shinkuma S, Watanabe M, Shigehara Y, Shimomura Y, Abe R.

J Dermatol. 2018 Jun 15. doi: 10.1111/1346-8138.14505. [Epub ahead of print] No abstract available.

PMID:
29905390
5.

Hailey-Hailey disease patient with a novel missense mutation in ATP2C1 successfully treated with minocycline hydrochloride.

Shigehara Y, Shinkuma S, Fujimoto A, Saijo S, Abe R.

J Dermatol. 2018 May 9. doi: 10.1111/1346-8138.14353. [Epub ahead of print] No abstract available.

PMID:
29740863
6.

Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family.

Takashima S, Shinkuma S, Fujita Y, Natsuga K, Nomura T, Hida T, Ishikawa S, Nakamura H, Abe R, Shimizu H.

J Dermatol. 2018 Mar 25. doi: 10.1111/1346-8138.14287. [Epub ahead of print] No abstract available.

PMID:
29574987
7.

Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes.

Nomura T, Suzuki S, Miyauchi T, Takeda M, Shinkuma S, Fujita Y, Nishie W, Akiyama M, Shimizu H.

JCI Insight. 2018 Mar 22;3(6). pii: 97595. doi: 10.1172/jci.insight.97595. [Epub ahead of print]

8.

Intravenous IgG Reduces Pathogenic Autoantibodies, Serum IL-6 Levels, and Disease Severity in Experimental Bullous Pemphigoid Models.

Sasaoka T, Ujiie H, Nishie W, Iwata H, Ishikawa M, Higashino H, Natsuga K, Shinkuma S, Shimizu H.

J Invest Dermatol. 2018 Jun;138(6):1260-1267. doi: 10.1016/j.jid.2018.01.005. Epub 2018 Jan 31.

PMID:
29391250
9.

Epidermal aspects of type VII collagen: Implications for dystrophic epidermolysis bullosa and epidermolysis bullosa acquisita.

Watanabe M, Natsuga K, Shinkuma S, Shimizu H.

J Dermatol. 2018 May;45(5):515-521. doi: 10.1111/1346-8138.14222. Epub 2018 Jan 20. Review.

PMID:
29352483
10.

Apocrine mixed tumour on the abdomen: an atypical location.

Mai S, Fujita Y, Sugai T, Imafuku K, Hata H, Shinkuma S, Nomura T, Kawagishi N, Shimizu H.

Eur J Dermatol. 2018 Apr 1;28(2):234-235. doi: 10.1684/ejd.2017.3200. No abstract available.

PMID:
29336312
11.

Establishment of integration-free induced pluripotent stem cells from human recessive dystrophic epidermolysis bullosa keratinocytes.

Matsumura W, Fujita Y, Nakayama C, Shinkuma S, Suzuki S, Nomura T, Abe R, Shimizu H.

J Dermatol Sci. 2018 Mar;89(3):263-271. doi: 10.1016/j.jdermsci.2017.11.017. Epub 2017 Dec 1.

PMID:
29229433
12.

Gentamicin-Induced Readthrough and Nonsense-Mediated mRNA Decay of SERPINB7 Nonsense Mutant Transcripts.

Ohguchi Y, Nomura T, Suzuki S, Takeda M, Miyauchi T, Mizuno O, Shinkuma S, Fujita Y, Nemoto O, Ono K, McLean WHI, Shimizu H.

J Invest Dermatol. 2018 Apr;138(4):836-843. doi: 10.1016/j.jid.2017.10.014. Epub 2017 Oct 26.

PMID:
29106929
13.

A solitary reddish nodule on the lower leg.

Miyazawa H, Shinkuma S, Yamaguchi Y, Fujita Y, Nomura T, Shimizu H.

Int J Dermatol. 2018 Mar;57(3):276-277. doi: 10.1111/ijd.13810. Epub 2017 Oct 26. No abstract available.

PMID:
29076158
14.

Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex.

Natsuga K, Nishie W, Nishimura M, Shinkuma S, Watanabe M, Izumi K, Nakamura H, Hirako Y, Shimizu H.

Hum Mutat. 2017 Dec;38(12):1666-1670. doi: 10.1002/humu.23344. Epub 2017 Oct 6.

PMID:
28941359
15.

Appearance of antidesmocollin 1 autoantibodies leading to a vegetative lesion in a patient with pemphigus vulgaris.

Yamaguchi Y, Shinkuma S, Ishii N, Takashima S, Natsuga K, Ujiie H, Iwata H, Nomura T, Fujita Y, Hamasaka A, Hamasaka K, Hashimoto T, Shimizu H.

Br J Dermatol. 2018 Jan;178(1):294-295. doi: 10.1111/bjd.15834. Epub 2017 Dec 3. No abstract available.

PMID:
28734006
16.

Type XVII collagen coordinates proliferation in the interfollicular epidermis.

Watanabe M, Natsuga K, Nishie W, Kobayashi Y, Donati G, Suzuki S, Fujimura Y, Tsukiyama T, Ujiie H, Shinkuma S, Nakamura H, Murakami M, Ozaki M, Nagayama M, Watt FM, Shimizu H.

Elife. 2017 Jul 11;6. pii: e26635. doi: 10.7554/eLife.26635.

17.

Generalized Pustular Psoriasis.

Kosumi H, Ito T, Fujita Y, Izumi K, Maya Y, Yanagi T, Natsuga K, Ujiie H, Shinkuma S, Nomura T, Sadanobu N, Shimizu H.

J Pediatr. 2017 Sep;188:305-305.e1. doi: 10.1016/j.jpeds.2017.05.058. Epub 2017 Jun 16. No abstract available.

PMID:
28629688
18.

Eosinophilic annular erythema is clinically characterized by central pigmentation reflecting basal melanosis: a clinicopathological study of 10 cases.

Nakazato S, Fujita Y, Shinkuma S, Nomura T, Shimizu H.

J Eur Acad Dermatol Venereol. 2017 Nov;31(11):1916-1923. doi: 10.1111/jdv.14350. Epub 2017 Jun 21.

PMID:
28543605
19.

A case of recessive dystrophic epidermolysis bullosa with a novel c.6885_6898del14 mutation in the COL7A1 gene.

Shinkuma S, Masunaga T, Miyawaki S, Takashima S, Natsuga K, Nomura T, Fujita Y, Nakamura H, Shimizu H.

J Dermatol Sci. 2017 Oct;88(1):139-141. doi: 10.1016/j.jdermsci.2017.03.022. Epub 2017 Apr 10. No abstract available.

PMID:
28427821
20.

Late-onset skin involvement on the forehead in multicentric Castleman disease.

Sato K, Shinkuma S, Fujimoto K, Hatanaka KC, Ujiie H, Nomura T, Fujita Y, Abe R, Matsuno Y, Shimizu H.

Int J Dermatol. 2017 Jul;56(7):e152-e153. doi: 10.1111/ijd.13559. Epub 2017 Feb 27. No abstract available.

PMID:
28244070

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