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Research 61–90 of 1000+
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Diffuse face and ear hypertrichosis caused by 5% topical minoxidil in an adult woman with spontaneous resolution
- Disorders of hair in children
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Drug-induced changes in hair growth
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- Hair physiology and its disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Pregnancy and Skin
- Genetics of Structural Hair Disorders
- Ingestion of topical steroid triggering pustular psoriasis?
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Acquired Localized Hypertrichosis Induced by Rivastigmine
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Causes and Management of Hypertrichosis
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Laser Hair Reduction and Removal
- Drug eruptions in dermatology
- Reply
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Momentary fluke of cyclosporine in incidental repigmentation and hypertrichosis of hair
- Describing the Hair and Related Abnormalities
- Biology and Genetics of Hair
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis