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Research 841–870 of 1000+
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- 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
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Alopecia - the search for novel agents continues
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Focal and Generalized Alopecia
- Alopecia: Association with Resistance to Thyroid Hormones
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Disease causing homozygous variants in the human hairless gene
- Alopecia in women submitted to childhood X-ray epilation for tinea capitis treatment
- Lectinhistochemistry of Dorsal Skin of Wistar-derived Hypotrichotic WBN/Ila-Ht Rats.
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Acquired progressive kinking of hair affecting the scalp and eyelashes in an adult woman
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Male Pattern Baldness
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Reversal of andro-genetic alopecia in a male. A spironolactone effect?