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Research 31–60 of 1000+
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- Skin fragility in the wild-derived, inbred mouse strain Mus pahari/EiJ
- Prior facility affects alopecia in adulthood for rhesus macaques
- Update on detection, morphology and fragility in pili annulati in three kindreds
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Cutaneous Toxicities From Transplantation-Related Medications
- Ten pearls every dermatologist should know about the appropriate use of relaxers
- Anatomical and Dermatologic Manifestations of Estrogen Deficiency in Postmenopausal Women: A Systematic Review
- Trichothiodystrophy in a child with occult learning disorder
- Monilethrix in three generations
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Dermatologic Manifestations In Chronic Kidney Disease Patients On Hemodialysis
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Monilethrix – Case report of a rare disease
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- CellTissueScience 2018: Innovations in regenerative medicine that improve the results of stem cell treatment: 3D cultivation, in vivo modeling of stem cell niche and prenatal stem cells exosomes_AbhijitBopardikar_ReeLabs Pvt. Ltd., India
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Keratins and disease at a glance
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Generalized atrophic benign epidermolysis bullosa.
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Follicular Unit Extraction
- Investigation of age-related decline of microfibril-associated glycoprotein-1 in human skin through immunohistochemistry study
- Trichorrhexis nodosa: a distinctive presentation after tumour necrosis factor-α inhibitor therapy
- Value of dermoscopy for the diagnosis of monilethrix