43 results on '"Akiyama, Masashi"'
Search Results
2. Two Cases of Porokeratosis with MVD Mutations, in Association with Bullous Pemphigoid.
3. Recurrent KRT10 Variant in Ichthyosis with Confetti.
4. Annular Sarcoidosis with Geographic Appearance in a Patient with Systemic Sarcoidosis.
5. Oculodentodigital Dysplasia Diagnosed from Severe Hypotrichosis.
6. A Japanese Case of Galli-Galli Disease due to a Previously Unreported POGLUT1 Mutation.
7. Dipeptidyl Peptidase-4 Inhibitor-associated Bullous Pemphigoid: Recurrence with Epitope Spreading.
8. Adult Staphylococcal Scalded Skin Syndrome Successfully Treated with Multimodal Therapy Including Intravenous Immunoglobulin.
9. Abscopal Effect of Local Irradiation Treatment for Diffuse Large B-cell Lymphoma.
10. Congenital Ichthyosis and Recurrent Eczema Associated with a Novel ALOXE3 Mutation.
11. Striate Palmoplantar Keratoderma Showing Transgrediens in a Patient Harbouring Heterozygous Nonsense Mutations in Both DSG1 and SERPINB7.
12. Recurrent Cellulitis Caused by Helicobacter cinaedi in a Patient with X-linked Agammaglobulinaemia.
13. Epstein-Barr Virus-associated Natural Killer/T-cell Lymphoma in a Patient Receiving Therapy with Anti-Tumour Necrosis Factor and Thiopurine.
14. Angiofibroma of Soft Tissue on the Cheek: Diagnosis Confirmed by Gene Rearrangement in NCOA2.
15. Epididymitis with Epididymal Cyst Indicating Immunoglobulin A Vasculitis in an AdultAi Nanbu, Kazumitsu Sugiura, Naoto Sassa, Masashi Akiyama.
16. Darier's Disease Complicated by Schizophrenia Caused by a Novel ATP2A2 Mutation.
17. A 45-year-old Woman with Ehlers-Danlos Syndrome Caused by Dermatan 4-O-sulfotransferase-1 Deficiency: Implications for Early Ageing.
18. Non-infectious Panniculitis during Hydroxyurea Therapy in a Patient with Myeloproliferative Disease.
19. Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function.
20. Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR.
21. What are the "true" pathogenic anti-desmoglein antibodies?
22. Lamellar ichthyosis caused by a previously unreported homozygous ALOXE3 mutation in East Asia.
23. Annular Elastolytic Giant Cell Granuloma Successfully Treated with Minocycline Hydrochloride.
24. TRPS1 Haploinsufficiency Results in Increased STAT3 and SOX9 mRNA Expression in Hair Follicles in Trichorhinophalangeal Syndrome.
25. Darier's disease: a novel ATP2A2 missense mutation at one of the calcium-binding residues.
26. Novel TGM1 missense mutation p.Arg727Gln in a case of self-healing collodion baby.
27. Annular erythema associated with Sjögren's syndrome preceding overlap syndrome of rheumatoid arthritis and polymyositis with anti-PL-12 autoantibodies.
28. Symmetrical giant facial plaque-type juvenile xanthogranuloma persisting beyond 10 years of age.
29. A novel ATP2C1 early truncation mutation suggests haploinsufficiency as a pathogenic mechanism in a patient with Hailey-Hailey disease.
30. A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex indicates the importance of the amino acid located at the boundary site between the H1 and coil 1A domains.
31. Sporadic VACTERL association in a Japanese family with Sjögren-Larsson syndrome.
32. Cryptococcal cellulitis in a patient with bullous pemphigoid.
33. Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.
34. Recurrence of hydroxyurea-induced leg ulcer after discontinuation of treatment.
35. Response of intractable skin ulcers in recessive dystrophic epidermolysis bullosa patients to an allogeneic cultured dermal substitute.
36. Successful treatment of nail lichen planus with topical tacrolimus.
37. Progressive refractory ulcer of the nipple: a quiz.
38. Keratitis-ichthyosis-deafness syndrome lacking subjective hearing impairment.
39. Diagnosis of Hailey-Hailey disease facilitated by DNA testing: a novel mutation in ATP2C1.
40. Multiple skin metastases of amelanotic melanoma originating from the sinonasal mucosa.
41. Association of infantile cutaneous haemangioma on the face and neck with respiratory distress in infancy.
42. Spitz naevus of the glans penis: an unusual location.
43. Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: immunohistological, ultrastructural and genetic studies.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.