Search
for
Sort by
Research 451–480 of 1000+
- Cutaneous Manifestations of Lupus Erythematosus
- Polycystic Ovary Syndrome in Adolescents
- Australasian Society for Dermatology Research Meeting, May 2006
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Fluridil, a Rationally Designed Topical Agent for Androgenetic Alopecia
- Histopathology of alopecia: a clinicopathological approach to diagnosis
- Relationship Between Androgen Levels and Blood Pressure in Young Women With Polycystic Ovary Syndrome
- Loose anagen hair of childhood: The phenomenon of easily pluckable hair
- ANDROGENETIC ALOPECIA
- Topical L‐thyroxine: The Cinderella among hormones waiting to dance on the floor of dermatological therapy?
- Particularidades dermatológicas, fisiológicas e as dermatoses na pele negra
- Farmácia Avenida Brasil, Porto
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Síndrome PRIDE: una práctica forma de identificar los efectos adversos cutáneos de los inhibidores del EGFR
- Neuroendocrine Controls of Keratin Expression in Human Skin
- TONGUE, RED
- Clinical and dermatoscopic features of temporal triangular alopecia in infants
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Renbök Phenomenon in a Patient With Alopecia Areata Universalis
- Trichoscopy as an essential diagnostic technique for hair and scalp disorders in skin of color: A case-control study
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Widespread and eruptive comedonal lesions with alopecia
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Whisker hair (acquired progressive kinking of the hair): An indication for finasteride 1 mg?
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- The Dual Nature of Cellular Senescence: From Aging Signature to Regenerative Catalyst
- Poliosis circumscripta: Overview and underlying causes
- The molecular basis of human keratin disorders