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Research 391–420 of 1000+
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- Hair aging and anti-aging
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Diagnosis and management of hair loss in children
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Syndromes of Severe Insulin Resistance (SSIRs)
- Main Plenary Sessions: Summaries of Papers
- Lupus erythematosus: systemic and cutaneous manifestations
- Morphological Approach to Hair Disorders
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Spironolactone, a Classic Potassium-Sparing Diuretic, Reduces Survivin Expression and Chemosensitizes Cancer Cells to Non-DNA-Damaging Anticancer Drugs
- Hyperadrenocorticism in Ferrets
- Caring for women with polycystic ovary syndrome
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- Ethnopharmacology and hair: Indian perspectives
- National scientific medical meeting 1996 abstracts
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>