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Research 61–90 of 1000+
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Delayed Puberty
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Acne-Associated Syndromes
- Painful thickened skin on the soles of the feet
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- Moniletherix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Loose Anagen Syndrome
- Dermatomyositis Disease in Dogs
- Hair dysplasias
- Androgenic alopecia and differential diagnoses of alopecia
- Clinical cases of Darier-White follicular dyskeratosis
- The Case | Bilateral kidney tumors and lung cysts
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- A newborn presenting with congenital blistering
- Monilethrix, a rare inherited hair shaft disorder in siblings
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair Anomalies in a 6-Year-Old Girl
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Diagnostic approach to low‐renin hypertension