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Research 241–270 of 1000+
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Keratins: the hair shaft's backbone revealed
- Recent advances in the genetics of alopecia areata
- Uncombable hair in a case of Zellweger syndrome – A new association
- Mind the hair
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Central hair loss in African American women: Incidence and potential risk factors
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Viewpoint 1
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Hair India 2010
- Trichotillomania Across Circuits: Neurobiology, Sensory Processing, and Genetic Insights
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Open questions in hidradenitis suppurativa research: a hair biologist's perspective
- The Review on Alopecia Areata : A Comprehensive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- Pearly Pinna Papules in a Young Female
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Adipocyte Lineage Cells Contribute to the Skin Stem Cell Niche to Drive Hair Cycling
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Disorders of ovulation
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix