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- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- Scarring Folliculitis in the Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome
- Noninflammatory, Nonpruritic Alopecia of Horses
- Hereditary, Congenital, and Acquired Alopecias
- Follicular dysplasia in two cows
- Concurrent follicular dysplasia and interface dermatitis in Boxer dogs
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Genetics of Structural Hair Disorders
- Congenital atrichia and hypotrichosis
- Ectodermal Dysplasia: Variable Expressions
- Inherited Disorders of the Hair
- Trichoscopy in Hair Shaft Disorders
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Dermatopathology and molecular genetics
- Analogs of human genetic skin disease in domesticated animals
- Commonly associated disorders with complete scalp alopecia in early childhood: A review