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- Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
- Cutaneous Lupus Erythematosus
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Lepromatous Leprosy in a Renal Transplant Recipient
- Ulcerative colitis and total alopecia in a mother and her son
- Dermatological adverse events with taxane chemotherapy
- Cutaneous lupus erythematosus
- General Dermatology
- Navigating Rhupus Complexity
- Navigating Rhupus Complexity
- Subacute cutaneous lupus erythematosus presenting as erythroderma
- Alopecia Areata, Primary Sclerosing Cholangitis, and Ulcerative Colitis: Autoimmunity and Apoptosis as Common Links?
- LUPUS ERYTHEMATOSUS AND THE SKIN
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Long‐term outcome after hand and forearm transplantation – a retrospective study
- Morphometric prediction of mesenchymal stromal cell-like immunosuppressive capacity of human hair follicle dermal sheath cup cells: an implication for regenerative medicine in hair loss diseases
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- HLA-B27 Antigen in Women With Ankylosing Spondylitis
- Changes in Populations of HLA- DR+CD3+ Cells and CD57–CD16+ Cells in Alopecia areata after Corticosteroid Therapy
- Alopecia areata after HLA-identical BMT from an affected, sibling donor
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?