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Research 30 of 644
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Lithium therapy associated with hidradenitis suppurativa: Case report and a review of the dermatologic side effects of lithium
- Dermatopathology and molecular genetics
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermoscopy in General Dermatology: A Practical Overview
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Inherited Disorders of the Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mucocutaneous reactions to chemotherapy
- Obesity and the skin
- Biology and Genetics of Hair
- Dermatologic Manifestations of Human Immunodeficiency Virus Infection
- Oral Retinoids in Dermatology
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- Hair Loss in Children
- Yellow and orange in cutaneous lesions: clinical and dermoscopic data
- Congenital atrichia and hypotrichosis
- Molecular Genetics of Alopecias
- Non‐infective mucocutaneous presentations of human immunodeficiency virus infection
- Skin manifestations of endocrine diseases
- Marie-unna hereditary hypotrichosis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Spatial variation and associated genes of total hair follicle density in goats
- Trichodystrophies: A hair-raising differential diagnosis
- Plaque psoriasis
- Signal Mining for Non-Bleeding Adverse Event in Novel Oral Anticoagulants: A Pharmacovigilance Study Based on the FAERS Database
- The skin and obesity
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- General Dermatology