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Research 691–720 of 1000+
- 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
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- 575 An extract of Leontopodium alpinum prolongs anagen phase in human hair follicles ex vivo
- 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
- Update on Frontal Fibrosing Alopecia
- 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
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Nonclassic Congenital Adrenal Hyperplasia
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- 5-Alpha reductase deficiency
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese