Search
for
Sort by
Research 631–660 of 1000+
- FOXN1 deficient nude severe combined immunodeficiency
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Molecular Mechanisms Responsible for Therapeutic Potential of Mesenchymal Stem Cell-Derived Secretome
- Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Androgen Receptor Polymorphisms (CAG Repeat Lengths) in Androgenetic Alopecia, Hirsutism, and Acne
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- The Pathogenesis of Primary Cicatricial Alopecias
- Lupus erythematosus: systemic and cutaneous manifestations
- Antiretroviral nucleoside and nucleotide analogues and mitochondria
- Male-pattern baldness susceptibility locus at 20p11
- Aging of hair
- Lichen planus pigmentosus and its variants: review and update
- Molecular basis of androgen receptor diseases
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- What causes hidradenitis suppurativa ?—15 years after
- Methotrexate in dermatology
- Cutaneous lupus erythematosus
- 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.
- Alopecia areata − animal models
- Dermoscopy for the Pediatric Dermatologist Part I: Dermoscopy of Pediatric Infectious and Inflammatory Skin Lesions and Hair Disorders
- Perspectives of Kennedy's disease
- How to diagnose a lipodystrophy syndrome
- Characteristics of Androgenetic Alopecia in Asian
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management