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Research 241–270 of 1000+
- The genetics of androgenetic alopecia
- Family History and Risk of Hair Loss
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Genes for Hair and Avian Keratins
- Dr Shoji Okuda (1886-1962): The great pioneer of punch graft hair transplantation
- Cantú syndrome with coexisting familial pituitary adenoma
- Kerion
- Albert kligman, also a hair man
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Alopecia: Association with Resistance to Thyroid Hormones
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Keratin 75 Is a Component of the LINC Complex and Has an Essential Role in Mediating the SOX2 Rapid Healing Response during Wound Repair
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Misspelling of Coauthor Surname
- Isolated long white eyelash: An underrecognized trichologic finding
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- An overview of risk factors for androgenetic alopecia among women at Pasar Ambacang, Kuranji, Padang
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- [Translated article] Frontal Fibrosing Alopecia and Lichen Planus Pigmentosus: Variants of the Same Disease?
- EXAMINATION OF NURSING STUDENTS' ACCEPTANCE LEVELS FOR AESTHETIC SURGERY AND AFFECTING FACTORS
- Pubertät
- Missing Conflict of Interest Disclosure
- Adams–Oliver syndrome: new evidence in variable expressivity?
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- 유전성 안드로겐탈모증 여성환자의 임상양상과 혈중 dehydroepiandrosterone sulfate 및 total testosterone 치
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- The voices of adult offspring of sperm donation: forces for change within assisted reproductive technology in the United States