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Research 61–90 of 1000+
- Acquired smooth muscle hamartoma with sebaceous component
- Traumatic panniculitis with hypertrichosis
- Coat Problems
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Disorders of the Hair and Nails
- Hair Disorders
- Generalized hypertrichosis associated with the use of interleukin 17 blockers in 2 patients with psoriasis
- Generalized hypertrichosis due to secukinumab in a patient with moderate psoriasis: A case of serendipity or zemblanity?
- Acquired scalp alopecia. Part II: A review
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Congenital atrichia and hypotrichosis
- Acquired Uncombable Hair
- 1371 FGF7-dependent inhibition of human hair growth byan osteopontin-derived peptide: A novel solution for hirsutism and hypertrichosis?
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Capryloyl glycine and soy isoflavonoids in hypertrichosis: An experimental and placebo‐controlled clinical study
- Ipsilateral post-cast hypertrichosis and dyshidrotic dermatitis
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Bimatoprost in the treatment of eyelash hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Female Adolescent Hair Disorders
- Drug-Induced Hair Loss and Hair Growth
- Biology and Genetics of Hair