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Research 31–60 of 1000+
- Hereditary, Congenital, and Acquired Alopecias
- Hereditary, Congenital, and Acquired Alopecias
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Hypertrichosis
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Hypertrichosis in Childhood
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- A rare clinical image of hypertrichosis (Werewolf syndrome)
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Congenital erythropoietic porphyria five years observation with standard treatment: a case report
- Hirsutism and Hypertrichosis
- 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.
- Office Diagnosis of Hair Shaft Defects
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- 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
- Cantú Syndrome Is Caused by Mutations in ABCC9
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)