All Stories

  1. HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy
  2. Difference in distribution of malignant melanoma and melanocytic nevus in the palm and finger
  3. Distribution analysis of infantile hemangioma or capillary malformation on the head and face in Japanese patients
  4. Psoriatic arthritis induced by anti‐programmed death 1 antibody pembrolizumab
  5. Anticomplement therapy in bullous pemphigoid
  6. Beneficial effect of methotrexate on a child case of Nakajo–Nishimura syndrome
  7. Peripheral blood eosinophilia is associated with the presence of skin ulcers in patients with systemic sclerosis
  8. Identification of a novel CCDC22 mutation in a patient with severe Epstein–Barr virus-associated hemophagocytic lymphohistiocytosis and aggressive natural killer cell leukemia
  9. CO2 narcosis as a notable cause of premature death in Nakajo-Nishimura syndrome
  10. Prognostic factors of daily blood examination for advanced melanoma patients treated with nivolumab
  11. Autoinflammatory Disorders Showing Pernio-like Eruptions
  12. Pluripotent Stem Cell Model of Nakajo-Nishimura Syndrome Untangles Proinflammatory Pathways Mediated by Oxidative Stress
  13. Repeated hyperhidrosis and chilblain-like swelling with ulceration of the fingers and toes in hereditary sensory and autonomic neuropathy type II
  14. Novel PSTPIP1 gene mutation in pyoderma gangrenosum, acne and suppurative hidradenitis syndrome
  15. WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study
  16. Severer lupus erythematosus-like skin lesions in MRL/lpr mice with homozygous Kitwsh/wsh mutation
  17. Depletion of Epidermal Langerhans Cells in the Skin Lesions of Pellagra Patients
  18. Guideline for the diagnosis and treatment of scabies in Japan (third edition)
  19. A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene
  20. Immunodeficiencies, autoinflammatory diseases and Hansen’s disease
  21. Case of Legionella pneumophila pneumonia (legionellosis) developed in a psoriatic arthritis patient receiving adalimumab
  22. A Case of Blau Syndrome withNOD2E383K Mutation
  23. Multiple courses of pulse corticosteroid therapy for alopecia areata
  24. Intractable leg ulcers in Blau syndrome
  25. The effect of hydroxychloroquine on lupus erythematosus-like skin lesions in MRL/lpr mice
  26. Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency
  27. A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome
  28. Pediatric pustular psoriasis with Turner's syndrome
  29. A Japanese Family with Congenital Erythrocytosis Caused by Haemoglobin Bethesda
  30. Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model
  31. Is CANDLE the best nomenclature?
  32. Autoimmunity versus Autoinflammation - Friend or Foe?
  33. Involvement of FcεR1α immunopositive cells in alopecia areata with atopic dermatitis and a high titer of serum immunoglobulin E
  34. Cancer, Infection and Disturbances of The Integrity of Tissue Homeostasis: The Most Significant Triggers for Molecular Mimicry and Autoimmunity in Dermatology?
  35. Hereditary Disorders Presenting with Urticaria
  36. Pachyonychia congenita in Japan: report of familial cases with a recurrent KRT16 mutation
  37. Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome
  38. NovelIL36RNmutation in a Japanese case of early onset generalized pustular psoriasis
  39. Monogenic early-onset sarcoidosis is no longer a variant of “idiopathic” sarcoidosis
  40. Atypical fibroxanthoma—a diagnosis of exclusion!
  41. A New Infant Case of Nakajo-Nishimura Syndrome with a Genetic Mutation in the Immunoproteasome Subunit: An Overlapping Entity with JMP and CANDLE Syndrome Related toPSMB8Mutations
  42. Comprehensive Review of Rare Hereditary Autoinflammatory Disorders
  43. Onychomycosis: modern diagnostic and treatment approaches
  44. Severe ulceration with impaired induction of growth factors and cytokines in keratinocytes after trichloroacetic acid application on TRPV1-deficient mice
  45. Rare hereditary autoinflammatory disorders: Towards an understanding of critical in vivo inflammatory pathways
  46. Influence of chemical peeling on the skin stress response system
  47. Sarcoidosis and molecular mimicry—important etiopathogenetic aspects: current state and future directions
  48. Nakajo-Nishimura Syndrome: An Autoinflammatory Disorder Showing Pernio-Like Rashes and Progressive Partial Lipodystrophy
  49. Hydroxychloroquine administration for Japanese lupus erythematosus in Wakayama: A pilot study
  50. Effects of sarpogrelate hydrochloride on skin ulcers and quality of life in patients with systemic sclerosis
  51. Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome
  52. Autoimmunity versus autoinflammation
  53. Steady state migratory RelB+ langerin+ dermal dendritic cells mediate peripheral induction of antigen-specific CD4+CD25+Foxp3+ regulatory T cells
  54. Preliminary study of etidronate for prevention of corticosteroid-induced osteoporosis caused by oral glucocorticoid therapy
  55. Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
  56. Nakajo-Nishimura Syndrome
  57. Influence of trichloroacetic acid peeling on the skin stress response system
  58. Case of anti-laminin-γ1 pemphigoid associated with psoriatic erythroderma
  59. Pathogenesis of cutaneous lupus erythematosus from LE-prone mice
  60. Effective treatment of intractable skin ulcers using allogeneic cultured dermal substitutes in patients with systemic lupus erythematosus
  61. No involvement of the NOD1 polymorphism Glu266Lys in Japanese leprosy patients
  62. Race Differences in Immunogenetic Features and Photosensitivity of Cutaneous Lupus Erythematosus from the Aspect of Japanese Studies
  63. Genotyping ofTrichophyton tonsuransisolate from a Japanese boy reveals infection in the USA
  64. Mast cells and histamine metabolism in skin lesions from MRL/MP-lpr/lpr mice
  65. No involvement of non-synonymous TLR2 polymorphisms in Japanese leprosy patients
  66. Efficacy and Safety of Ebastine (EBASTEL) for Pruritic Skin Disease-Evaluation of High-dose Administration-
  67. Genetic involvement of bacterial sensor molecules in Japanese leprosy
  68. Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis
  69. The Protective Effects of Ultraviolet A1 Irradiation on Spontaneous Lupus Erythematosus-Like Skin Lesions in MRL/lpr Mice
  70. Cutaneous polyarteritis nodosa: revisiting its definition and diagnostic criteria
  71. Guideline for the diagnosis and treatment of scabies in Japan (second edition)
  72. Autoinflammatory syndromes with a dermatological perspective
  73. Induction of PDGF-B in TCA-treated epidermal keratinocytes
  74. Dendritic cell immunoreceptors: C-type lectin receptors for pattern-recognition and signaling on antigen-presenting cells
  75. Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations
  76. Disease-associated mutations in CIAS1 induce cathepsin B–dependent rapid cell death of human THP-1 monocytic cells
  77. Expression of prostate-specific antigen and androgen receptor in extramammary Paget's disease and carcinoma
  78. The cytosolic pattern-recognition receptor Nod2 and inflammatory granulomatous disorders
  79. The Conduit System Transports Soluble Antigens from the Afferent Lymph to Resident Dendritic Cells in the T Cell Area of the Lymph Node
  80. Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor- B activation: common genetic etiology with Blau syndrome
  81. Signaling and immune regulatory role of the dendritic cell immunoreceptor (DCIR) family lectins: DCIR, DCAR, dectin-2 and BDCA-2
  82. Molecular Cloning of Human Dectin-2
  83. Presence of a Sporadic Case of Systemic Granulomatosis Syndrome with a CARD15 Mutation
  84. Dendritic Cell Immunoactivating Receptor, a Novel C-type Lectin Immunoreceptor, Acts as an Activating Receptor through Association with Fc Receptor γ Chain
  85. DCIR Acts as an Inhibitory Receptor Depending on its Immunoreceptor Tyrosine-Based Inhibitory Motif11A preliminary report of these results was presented by the first author at the 61st annual meeting of SID in Chicago in the session “General Immunology”.
  86. Fractalkine and macrophage-derived chemokine: T cell-attracting chemokines expressed in T cell area dendritic cells
  87. Molecular Cloning, Characterization, and Chromosomal Localization of FKBP23, a Novel FK506-Binding Protein with Ca2+-Binding Ability
  88. Human Calumenin Gene (CALU): cDNA Isolation and Chromosomal Mapping to 7q32
  89. Expression of bcl-6 protein in normal skin and epidermal neoplasms
  90. Calumenin, a Ca2+-binding Protein Retained in the Endoplasmic Reticulum with a Novel Carboxyl-terminal Sequence, HDEF