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Research 451–480 of 1000+
- An evaluation of the safety and efficacy of bimatoprost for eyelash growth in pediatric subjects
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Dermoscopy: A rapid bedside tool to assess monilethrix
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Alopecia Universalis Associated with Ulcerative Colitis and The Role of Azathioprine
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Discreet monilethrix: De novo mutation on the example of polish families
- Erythromelanosis Follicularis Faciei: First Case Report from Saudi Arabia
- Multimodal Reconstructive Treatment of the Face and Scalp Following Catastrophic Burn Injury: An Eight-Year Experience with Structural Fat Grafting, Follicular Unit Excision Hair Transplantation, and Scalp Micropigmentation
- Hair Care and Hair‐Focused Repetitive Behaviors: A Descriptive Cross‐Sectional Study
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Considerations for the Treatment Strategy of Relapse After Tofacitinib Therapy in Alopecia Areata
- Gloriosa superba Poisoning-induced Anagen Effluvium
- Case Report: Baricitinib improved alopecia areata in a pediatric patient with atopic dermatitis
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Monilethrix – Case report of a rare disease
- Trichothiodystrophy in a child with occult learning disorder
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Evaluating the Therapeutic Potential of Ritlecitinib for the Treatment of Alopecia Areata
- Novel treatment of female-pattern androgenetic alopecia with injected bimatoprost 0.03% solution.
- Common causes of paediatric alopecia
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report