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Research 91–120 of 1000+
- Alopecia
- Book Reviews
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- The amazing miniorgan: Hair follicle
- Clinical Management in Psychodermatology
- ATP-dependent chromatin remodeling during mammalian development
- Morpho-Regulation of Ectodermal Organs
- 9 Role of 5α-reductase in health and disease
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Polycystic Ovary Syndrome and Its Differential Diagnosis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- New changes in pregnancy and lactation labelling: Review of dermatologic drugs
- Improving Posttraumatic Facial Scars
- The Function of Zinc in Animal, Plant, and Human Nutrition
- Ottawa, Ontario, Canada, February 13–16, 2013
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Inherited Epidermolysis Bullosa: A Clinical Case
- Program and Abstract of 16th APALMS 2018
- Minoxidil
- Hyperplasia of the Subcutaneous Adipose Tissue Is the Primary Histopathologic Abnormality in Lipedematous Scalp
- Techniques d'épargne cutanée dans la chirurgie de la gynécomastie
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Particularidades dermatológicas, fisiológicas e as dermatoses na pele negra
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- Congenital atrichia associated with situs inversus and mesocardia
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Restoration of skin pigmentation after deep partial or full-thickness burn injury
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle