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- 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
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- Linking allergy to mercury to HLA and burning mouth syndrome
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Alopecia Areata
- THE PATHOGENESIS OF ALOPECIA AREATA
- Cutaneous Lupus Erythematosus
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