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Research 571–600 of 1000+
- Polarized microscopy in genetic hair disorders: case series
- Woolly hair generalizado: caso clínico e revisão da literatura
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Evaluation of hair structural abnormalities in children with different neurological diseases
- Color dilution alopecia in a Yorkshire
- Clinical and molecular genetic studies in hereditary hair loss
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Index
- Pathology in Practice
- Nutritional Skin Diseases
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Efeitos da ingestão de cafeína durante a gestação e a lactação sobre a pele de ratas e de filhotes e sua relação com as concentrações séricas do cortisol materno
- Pubic Hair Transplant
- Displasia folicular en un Doberman adulto de capa negra : un caso clínico
- Laser hair removal
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Management of androgenetic alopecia
- Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia
- Familial and Sporadic Porphyria Cutanea Tarda
- Off-Label Use of Topical Minoxidil in Alopecia: A Review
- Understanding and Management of Female Pattern Alopecia
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Very-low-dose oral minoxidil in male androgenetic alopecia: A study with quantitative trichoscopic documentation
- Phosphodiesterase inhibitors and prostaglandin analogues in dermatology: A comprehensive review
- Low-dose oral minoxidil for treatment of androgenetic alopecia and telogen effluvium in a pediatric population: A descriptive study