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Research 31–60 of 1000+
- Keratosis follicularis spinulosa decalvans in a family
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Androgenic alopecia and differential diagnoses of alopecia
- Clinical cases of Darier-White follicular dyskeratosis
- Delayed Puberty
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Dermatomyositis Disease in Dogs
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Two females with hair loss
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Monilethrix in three generations
- Dermoscopic Features of Pili Annulati: Features of PA