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Research 601–630 of 1000+
- Phrynoderma and acquired acrodermatitis enteropathica in breastfeeding women after bariatric surgery
- Alopecia in children
- Value of dermoscopy for the diagnosis of monilethrix
- Fibrosing alopecia in a pattern distribution
- Pattern alopecia in a miniature pinscher dog
- Gli ebrei nelle prime "ordinanze" di castello di cagliari (1347). Nota per una rilettura etnologica
- [A systemic-like disease: chronic vitamin A poisoning].
- Cutaneous Side Effects of Oral Contraceptives
- How real is senescent alopecia? A histopathologic approach
- Das idiopathische chronische Telogeneffluvium der Frau
- Scalp Psoriasiform Contact Dermatitis with Acute Telogen Effluvium due to Topical Minoxidil Treatment
- Oral Isotretinoin in HIV-Positive Women with Acne: Report of Three Cases
- Alopecia areata and subsequent Marie Antoinette syndrome following COVID-19 infection and vaccination: A case report
- Diagnosis: Alopecia areata or not?
- Amyopathic dermatomyositis presenting as severe alopecia and prominent eyelid edema: a case report and literature review
- Gloriosa superba Poisoning-induced Anagen Effluvium
- The Need to Analyze Telogen Effluvium and Alopecia Areata Parallelly in Long COVID Studies
- Clinical Toxicityof Retinoids
- A case of telogen effluvium associated with drug-induced hyperprolactinemia.
- Functional analysis of collagen XVII in epithelial cancers and a mouse model
- CME examination
- Management of female androgenetic alopecia
- P132 Quality of life, psychopathologic symptoms and personality disorders in subjects with androgenetic alopecia
- Trichoscopy
- Micturitional disturbance in a patient with adrenomyeloneuropathy (AMN)
- Fulminant systemic vasculitis in systemic lupus erythematosus. Case report and review of the literature
- Cronkhite–Canada Syndrome Diagnosis in the Absence of Gastrointestinal Polyps
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- [Drug induced alopecia].
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>