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Research 61–90 of 594
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Advances in Platelet Rich Plasma-Derived Extracellular Vesicles for Regenerative Medicine: A Systematic-Narrative Review
- Managing Dermatologic Effects of Gender-Affirming Therapy in Transgender Adolescents
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- An Overview of Alopecias
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Trichotillomania in Children
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Acquired constriction ring syndrome as a cause of inconsolable cry in a child: a case report
- Polycystic ovary syndrome
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Impacto del desequilibrio del microbioma del cuero cabelludo en la severidad de la alopecia areata, marcadores inflamatorios y cambios post-tratamiento
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- An unusual case report of rapunzel syndrome trichobezoar in a 3-year-old boy
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Dermatological medications and local therapeutics
- Drug-induced Telogen Effluvium in a Pediatric Patient due to Error of Transcription.
- Advancing mitochondrial therapeutics: Synthesis and pharmacological evaluation of pyrazole-based inhibitors targeting the mitochondrial pyruvate carrier
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Morphologic Markers of Acute and Chronic Stress in Child Abuse
- Herbal Approaches for the Management of Premature Hair Greying: Mechanisms, Phytoconstituents and Delivery Strategies
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Polarized microscopy in genetic hair disorders: case series
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Longitudinal clinical course, treatment outcomes, and relapse patterns in alopecia areata: a prospective cohort study