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Research 301–330 of 1000+
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- Microinfusão de metotrexato nas lesões de couro cabeludo podem auxiliar no alívio da alopécia frontal fibrosante?
- Treatment of Alopecia in Children
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Acquired ichthyosis, alopecia and loss of hair pigment associated with leiomyosarcoma.
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- FOXN1 deficient nude severe combined immunodeficiency
- Pili torti in association with citrullinemia
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Disorders of hair in infants and children other than alopecia
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Alopezien und Hypotrichosen im Kindesalter
- Patterns of noncicatricial alopecia in children: a cross-sectional study
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Ptosis in childhood
- An Approach to Hair Loss in Pediatric Primary Care
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice