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Research 31–60 of 1000+
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A new type of pachyonychia congenita.
- Alopezien und Hypotrichosen im Kindesalter
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Facial Hair Transplantation
- Office Diagnosis of Hair Shaft Defects
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Coat Problems
- Genetics of Alopecia
- A clinician's approach to canine alopecia
- Disorders of hair in children
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Dermatopathology and molecular genetics
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Woolly hair generalizado: caso clínico e revisão da literatura
- Clinical and molecular genetic studies in hereditary hair loss
- Polarized microscopy in genetic hair disorders: case series
- Index
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Congenital hair loss disorders: Rare, but not too rare
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort