Search
for
Sort by
Research 151–180 of 1000+
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Learning from nudity: lessons from the nude phenotype
- Molecular Regulation of Melanocyte Senescence
- Congenital hair loss disorders: Rare, but not too rare
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Recognition and management of <i>Staphylococcus aureus</i> toxin‐mediated disease
- Secondary cicatricial and other permanent alopecias
- Oral Retinoids in Dermatology
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- The role of vitamin D receptor mutations in the development of alopecia
- The molecular pathogenesis of Trichilemmal carcinoma
- Dermatologic care of patients with differences of sex development
- Ectodermal Dysplasia: Variable Expressions
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Congenital atrichia associated with situs inversus and mesocardia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- E-Poster