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Research 91–120 of 1000+
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Keratosis follicularis spinulosa decalvans in a family
- Birt–Hogg–Dubé syndrome
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- <i>De novo</i> mutations in monilethrix
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma
- A newborn presenting with congenital blistering
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Clinical cases of Darier-White follicular dyskeratosis
- Hair Anomalies in a 6-Year-Old Girl
- The Case | Bilateral kidney tumors and lung cysts
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Diagnostic approach to low‐renin hypertension
- 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
- Painful thickened skin on the soles of the feet
- Office Diagnosis of Hair Shaft Defects
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Monilethrix: Beaded hair and hypotrichosis in a child
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Monilethrix, a rare inherited hair shaft disorder in siblings