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Research 23
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Prenatal diagnosis of a foetus with partial monosomy 4p and partial trisomy 13q
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Genetic Defects of Female Sexual Differentiation
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Turner's syndrome associated with psoriasis and alopecia areata
- Morpho-Regulation of Ectodermal Organs
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- The ITGB6 gene: its role in experimental and clinical biology
- Gender differences in skin: A review of the literature
- Alisertib is active as single agent in recurrent atypical teratoid rhabdoid tumors in 4 children
- Metabolism and skin diseases
- Skin manifestations among<i>GATA2</i>-deficient patients
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Dermatologic care of patients with differences of sex development
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- A Case of Frontal Fibrosing Alopecia in a Patient with Primary Biliary Cirrhosis and Polymyalgia Rheumatica
- Cantú Syndrome Is Caused by Mutations in ABCC9
- The Genetics of Human Skin Disease
- 69-Year-Old Man With Dysuria and Right Lower Abdominal Pain