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Research 451–480 of 1000+
- Hair growth promoting effects of adipose tissue-derived stem cells
- Diet and hair loss: effects of nutrient deficiency and supplement use
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- 5-Alpha reductase deficiency
- Trichoscopy in Hair Shaft Disorders
- Cardiovascular risk factors and events in women with androgen excess
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Further Clinical Evidence for the Effect of IGF-1 on Hair Growth and Alopecia
- Endocrine evaluation of hirsutism
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Congenital adrenal hyperplasia
- Hydroxysteroid Dehydrogenase (17β -HSD3, 17β-HSD5, and 3α-HSD3) Inhibitors:Extragonadal Regulation of Intracellular Sex Steroid Hormone Levels
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- 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
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- 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
- Evolving approaches to profiling the microbiome in skin disease
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Molecular Genetics of Alopecias
- Focal and Generalized Alopecia