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Research 211–240 of 1000+
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Bubble hair and other acquired hair shaft anomalies due to hot ironing on wet hair
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Trichotillomania
- Diffuse Hair Loss
- The difficult hair loss patient: A particular challenge
- IDEA Group Consensus Statement on Medical Management of Adult Gender Incongruent Individuals Seeking Gender Affirmation as Male
- Notes from the Editor Emeritus
- Assessing the Efficacy of Multimodal Therapy in Nonsurgical Hair Restoration for Noncicatricial Alopecia: A Retrospective Study
- Mirtazapine-induced Gynecomastia: An Unknown Side Effect?
- Endocrine Management of Adult Gender-Dysphoric/Gender-Incongruent Persons: A Clinical Practice Guideline from Endocrine Society of India
- Understanding the Association Between Mental Health and Hair Loss
- Post‐Finasteride Syndrome or Pre‐Existing Vulnerability? Rethinking Patient Selection
- Evaluation of Dutasteride-Loaded Liposomes and Transfersomes for Follicular-Targeting for Androgenic Alopecia Topical Treatment
- Patient prioritisation of impact items to develop the patient‐reported impact of dermatological diseases (PRIDD) measure: European Delphi data
- Quantitative and qualitative analysis of individual experiences post botulinum toxin injection ‐ United Kingdom Survey
- Fade haircut or something else?
- A catena between psychiatric disorders and non‐scarring alopecias—A systematic review
- Trichotillomania with Giant Gastric Trichobezoar in a Female Child: A Case Report
- TRICHOTILLOMANIA WITH GIANT GASTRIC TRICHOBEZOAR IN A FEMALE CHILD: A CASE REPORT
- Acne Vulgaris
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Systemic lupus erythematosus presenting with homonymous hemianopia
- Contemporaneous onset of systemic lupus erythematosus and severe eating disorder; neither the chicken nor the egg