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Research 541–570 of 1000+
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- A new type of pachyonychia congenita.
- Eruptive Vellus Hair Cyst
- Masquerading of trichotillomania in a family with monilethrix
- Monilethrix in three generations
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Monilethrix
- Acquired Uncombable Hair
- Spangled hair in siblings
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Monilethrix
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Disorders of pigmentation in infants and children
- Alopecia in a 19-Month-Old Boy
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Acquired uncombable hair
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Ugreelig hår
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Dermoscopic Features of Pili Annulati: Features of PA
- Woolly hair generalizado: caso clínico e revisão da literatura
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Monilethrix with Acitretin
- Informàtica i Dret penal: Els delictes relatius a la informàtica