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Research 451–480 of 1000+
- Reconnection of cysteine in reduced hair with alkylene dimaleates via thiol‐Michael click chemistry
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Steroid Cell Tumor of the Ovary in an Adolescent: A Rare Case Report
- Lupeol: an updated review utilizing AI-assisted predictive tools for enhanced therapeutic insights into lupeol’s potential for alopecia management
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- Alopecia universalis with IL-12-RB1 and STAT4 mutations effectively treated with upadacitinib
- Case report: Sequential therapy with dupilumab and baricitinib for severe alopecia areata with atopic dermatitis in children
- A Large Benign Adrenocortical Adenoma Cosecreting Testosterone and Cortisol
- A 21-Day-Old Boy with an Annular Eruption
- An unusual presentation of X-linked adrenoleukodystrophy
- Exames laboratoriais como estratégia de personalização na prática estética
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- EtG Quantification in Hair and Different Reference Cut-Offs in Relation to Various Pathologies: A Scoping Review
- Understanding Curly Hair Mechanics: Fiber Strength
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Effect of Prunus Tomentosa Thumb Total Flavone on hair growth