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Research 361–390 of 1000+
- Hair dysplasias
- The Case | Bilateral kidney tumors and lung cysts
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Management of pregnancy in a carrier of the Donohue mutation
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Targeting integrin pathways: mechanisms and advances in therapy
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Diagnostic approach to low‐renin hypertension
- Delayed Puberty
- 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
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- [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