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Research 511–540 of 1000+
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Acne
- Hair aging and anti-aging
- Acne and acneiform eruptions
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Hair Disorders
- Lipid nanocarriers as innovative strategies for hair regrowth
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- National scientific medical meeting 1996 abstracts
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Answer
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Ovarian steroid cell tumor in a teenager masquerading as polycystic ovary syndrome: a case report and literature review
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Causes and Management of Hypertrichosis
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency