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Research 91–120 of 226
- The Genetics of Human Skin Disease
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Síndrome do nevo de Becker
- Hair and Nail Relationship
- Secondary cicatricial and other permanent alopecias
- Hair loss
- Successful induction of oral tolerance in Netherton syndrome
- Congenital atrichia and hypotrichosis
- Molecular Genetics of Alopecias
- Diseases of Periocular Hair
- Both low circulating insulin-like growth factor-1 and high-density lipoprotein cholesterol are associated with hair loss in middle-aged women
- Darier Sign: A Historical Note
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ
- ИСПОЛЬЗОВАНИЕ ПОЛИНУКЛЕОТИДОВ В АНТИВОЗРАСТНОЙ ИНЪЕКЦИОННОЙ КОСМЕТОЛОГИИ С ПОЗИЦИИ ДОКАЗАТЕЛЬНОЙ МЕДИЦИНЫ
- Immunological control of skin development: from homeostasis to developmental pathologies
- Bad Hair Days: A Clinical and Trichoscopic Evaluation of Scalp Lesions
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- 138 Characterization of xenobiotic metabolizing enzymes of a reconstructed human epidermal model from adult hair follicles
- BH07: Testosterone deficiency in men with female pattern hair loss
- Oral retinoids-present status
- Hair and scalp disorders in ethnic populations
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Disorders of hair
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Vulvovaginal involvement in Netherton syndrome: A case report
- Collodion baby case series: the success of oral retinoic acid