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Research 841–870 of 1000+
- Microneedling plus topical dutasteride solution for androgenetic alopecia: a randomized placebo‐controlled study
- A study of the Geheimratsacken angle as predictor for early diagnosis of androgenetic alopecia in adolescent population
- The Hair Shedding Visual Scale: A Quick Tool to Assess Hair Loss in Women
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Bioengineering the Hair Follicle
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth.
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Hair growth promoting effects of adipose tissue-derived stem cells
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- 5-Alpha reductase deficiency
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma