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Research 721–750 of 1000+
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- [Netherton's syndrome in two sisters].
- 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
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Hair That Is Difficult to Manage in a Hispanic Girl
- Acne-Associated Syndromes
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Monilethrix: Beaded hair and hypotrichosis in a child
- Assessment of scalp hair survivin in patients with premature greying of hair
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Reviewer #2 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Alopecia totalis in an infant
- Painful thickened skin on the soles of the feet
- Central Centrifugal Cicatricial Alopecia (CCCA)
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Clinical Snippets
- Clinical Snippets
- Polycystic ovarian disease in adult and perimenopausal women
- Office Diagnosis of Hair Shaft Defects