234 results on '"Niizeki, Hironori"'
Search Results
2. Safety and Efficacy of the Sirolimus Gel for TSC Patients With Facial Skin Lesions in a Long-Term, Open-Label, Extension, Uncontrolled Clinical Trial
3. Effectiveness of non-steroidal anti-inflammatory drugs among patients with primary hypertrophic osteoarthropathy: A systematic review
4. Transepidermal water loss measurement during infancy can predict the subsequent development of atopic dermatitis regardless of filaggrin mutations
5. Splicing abnormality of integrin β4 gene (ITGB4) due to nucleotide substitutions far from splice site underlies pyloric atresia-junctional epidermolysis bullosa syndrome
6. Application of moisturizer to neonates prevents development of atopic dermatitis
7. Delayed‐onset heat intolerance in a Japanese patient with X‐linked hypohidrotic ectodermal dysplasia associated with a large deletion involving four genes
8. Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene
9. Infiltration of mast cells in pachydermia of pachydermoperiostosis
10. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis
11. Role of Prostaglandin E-Major Urinary Metabolite Levels in Identifying the Phenotype of Pachydermoperiostosis
12. An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases
13. Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations
14. Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate-ectodermal dysplasia syndrome in an Asian patient
15. Pathological characterization of pachydermia in pachydermoperiostosis
16. Adjuvant effect of lipopolysaccharide on the induction of contact hypersensitivity to haptens in mice
17. Regulatory effects of antihistamines on the responses to staphylococcal enterotoxin B of human monocyte-derived dendritic cells and CD4 + T cells
18. Relationship among human herpesvirus 6 reactivation, serum interleukin 10 levels, and rash/graft-versus-host disease after allogeneic stem cell transplantation
19. Novel EDA hemizygous frame-shift mutation c. 731delG (p.R244Qfs*36) underlies hypohidrotic ectodermal dysplasia in a Japanese family
20. Grading criteria for disease severity by pemphigus disease area index
21. Japanese guidelines for the management of pemphigus
22. Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations
23. Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1
24. Compound Heterozygous Mutations Including a De Novo Missense Mutation in ABCA12 Led to a Case of Harlequin Ichthyosis with Moderate Clinical Severity
25. An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases.
26. A Distinct Feature of T Cell Subpopulations in a Patient with CHARGE Syndrome and Omenn Syndrome
27. Mosquito Salivary Gland Extracts Induce EBV-Infected NK Cell Oncogenesis Via CD4+ T Cells in Patients with Hypersensitivity to Mosquito Bites
28. Paraneoplastic pemphigus presenting as erythrodermic lichenoid dermatitis with concomitant features of pemphigus foliaceus
29. Role for connexin 26 in metastasis of human malignant melanoma: Communication between melanoma and endothelial cells via connexin 26
30. Occult myopathy of the vastus intermedius muscles detected by magnetic resonance imaging in subclinical dermatomyositis: report of two cases
31. Ampicillin-induced cutaneous eruption associated with Epstein-Barr virus reactivation
32. Induction of macrophage migration inhibitory factor precedes the onset of acute tonsillitis
33. A clinical feature associated with polymorphisms of the TNF region in Japanese patients with palmoplantar pustulosis
34. Local Ultraviolet B Irradiation Impairs Contact Hypersensitivity Induction by Triggering Release of Tumor Necrosis Factor-α from Mast Cells. Involvement of Mast Cells and Langerhans Cells in Susceptibility to Ultraviolet B
35. A Substance p Agonist Acts as an Adjuvant to Promote Hapten-Specific Skin Immunity
36. Neural Influences on Induction of Contact Hypersensitivity
37. Polymorphisms in the TNF region confer susceptibility to UVB-induced impairment of contact hypersensitivity induction in mice and humans
38. Hapten-Specific Tolerance Induced by Acute, Low-Dose Ultraviolet B Radiation of Skin Is Mediated via Interleukin-10
39. First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
40. Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations
41. A male Korean who was diagnosed with chronic enteropathy associated with SLCO2A1 (CEAS): case report with literature review
42. Congenital nail clubbing
43. Sirolimus Gel Treatment vs Placebo for Facial Angiofibromas in Patients With Tuberous Sclerosis Complex
44. Linear keratinocytic epidermal nevi on trunk skin caused by a somatic FGFR2 p.C382R mutation
45. Japanese case of xeroderma pigmentosum complementation group C with a novel mutation
46. Involvement of prostaglandin E2 in the first Japanese case of pachydermoperiostosis with HPGD mutation and recalcitrant leg ulcer
47. Delayed-onset heat intolerance in a Japanese patient with X-linked hypohidrotic ectodermal dysplasia associated with a large deletion involving four genes
48. Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family
49. Novel heterozygous deletion mutation c.821delC in the AAA domain of BCS1L underlies Björnstad syndrome
50. Mutations in SERPINB7, Encoding a Member of the Serine Protease Inhibitor Superfamily, Cause Nagashima-type Palmoplantar Keratosis
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