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Research 901–930 of 1000+
- Erosive pustular dermatosis of the scalp - is it really a rare condition?
- Acral lymphomatoid papulosis
- Rituximab for Bone Lymphoma
- Perspectives in Head and Neck Medical Oncology
- The effect of COVID‐19 on development of hair and nail disorders: a Turkish multicenter, controlled study
- Omeprazole-induced hypertrichosis in two children
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- An Evaluation System to Enhance Patient Selection for Alopecia-Reducing Surgery
- Pulmonary arterial aneurysm in Behçet's disease
- The urine as a diagnostic key for a homozygous EGFR mutation
- A previously undescribed cutaneous paraneoplastic syndrome in a cat with thymoma
- An unusual side effect of azathioprine
- A Child with Nonscarring Alopecia
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- A Prospective Longitudinal Study of Dynamic of Human Papillomavirus 6 and 11 Infection in Anogenital Hairs and Eyebrows of Male Patients with Anogenital Warts and Age-Matched Controls
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- 81 Juvenile RHUPUS syndrome: a case reports
- Trichotillomania in a young male complicated by tinea capitis associated with Cryptococcus laurentii and Candida parapsilosis
- Psychoneuroendocrinimmunodermatology
- [Association of a pediatric bullous eruption, cutaneous and muscular atrophy, hyperpigmentation and dysmorphism. A new entity?].
- NEW YORK DERMATOLOGICAL SOCIETY
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Pediatric alopecia areata managed with constitutional homoeopathy: A case report at Dr Batra’s
- The follicular microbiome in hair-follicle-associated inflammatory diseases: A systematic review
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Diagnosis and treatment of local forms of alopecia areata in children
- Role of Herbomineral Drugs in the Management of Diarrhea and Late Effects of Chemotherapy in the Patient of Oral Cavity Cancer