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Research 631–660 of 1000+
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- 575 An extract of Leontopodium alpinum prolongs anagen phase in human hair follicles ex vivo
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Skin signs of systemic diseases
- Hair shaft structures in EDAR induced ectodermal dysplasia
- 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
- 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Nonclassic Congenital Adrenal Hyperplasia
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Congenital adrenal hyperplasia
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- The Effect of Simvastatin on Plasma Steroid Hormone Levels in Metformin-Treated Women with Non-Classic Congenital Adrenal Hyperplasia
- Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- Abstracts
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Hemoglobinopathy and Systemic Lupus: A Rare Association