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Research 151–180 of 1000+
- Hair Anomalies in a 6-Year-Old Girl
- Hair dysplasias
- The Case | Bilateral kidney tumors and lung cysts
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Hair: more than just an appendage
- Targeting integrin pathways: mechanisms and advances in therapy
- Diagnostic approach to low‐renin hypertension
- Delayed Puberty
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- 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
- 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
- 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
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Painful thickened skin on the soles of the feet
- Dermatomyositis Disease in Dogs
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Polycystic ovarian disease in adult and perimenopausal women
- Office Diagnosis of Hair Shaft Defects
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis