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Research 61–90 of 574
- Hair Loss: A Harbinger of the Morbidities to Come!
- Woolly Antics between the Sheaths
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Hair Loss in Children
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- JAAD Grand Rounds quiz∗
- Hair That Is Difficult to Manage in a Hispanic Girl
- Biotin
- Keratin disorders: from gene to therapy
- Hair and Nail Manifestations of Systemic Disease
- Anagen effluvium
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Hypotrichosis in a child with olmsted syndrome
- The Genetics of Human Skin Disease
- Uveodermatological syndrome associated with alopecia areata in a one‐year‐old female spayed Cavalier King Charles Spaniel dog
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- [Frizzy hair pathology].
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Enanthem in Patients With COVID-19 and Skin Rash
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Genetic Hair Disorders: A Review