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Research 961–990 of 1000+
- A Systematic Review of Persistent Symptoms and Residual Abnormal Functioning following Acute COVID-19: Ongoing Symptomatic Phase vs. Post-COVID-19 Syndrome
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Symptoms Compatible With Long Coronavirus Disease (COVID) in Healthcare Workers With and Without Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection—Results of a Prospective Multicenter Cohort
- E031 Retinal vasculitis with Libman-Sacks endocarditis as presenting features of a systemic lupus erythematosus with antiphospholipid antibody syndrome patient
- 66-Year-Old Female with Itchy Scalp and Hair Loss
- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Clinical Spectrum of Cutaneous, Ocular, and Hair Manifestations in Patients With Inborn Errors of Immunity: Insights From a Single Center in Turkey
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Testosterone therapy for transgender men
- THE PATHOGENESIS OF ALOPECIA AREATA
- Acne as a chronic systemic disease
- Poliosis circumscripta: Overview and underlying causes
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- The Genetics of Human Skin Disease
- Séquelles cutanéomuqueuses et oculaires des SJS et de Lyell
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Metabolism and skin diseases
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- ALX4-related frontonasal dysplasia sequence presenting with alopecia in a 12 year old girl
- A Case Report of Association between Canine Hypothyroidism and Diabetes
- Eyelashes: Anatomical and Physiological Features, Eyelash Loss and Trichomegaly: Review
- Idiopathic isolated adrenocorticotropic hormone deficiency combined with testicular germ cell tumor: Case report
- The Role of Androgens in Health and Disease in Females: A Narratıve Review
- Reexamining the Role of Diet in Dermatology
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly