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Research 151–180 of 1000+
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- A guide to diagnosis and management of hypertrichosis
- Ichthyoses
- Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Stem Cells Applications in Regenerative Medicine and Disease Therapeutics
- Comparative Anatomy of Mouse and Human Nail Units
- Top applications of dermatologic ultrasonography that can modify management
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Study of the Thyroid Profile of Patients with Alopecia
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Frequency of neuro-psychiatric dysfunction in anti-SSA/SSB exposed children with and without neonatal lupus
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- Ectodermal Dysplasia: Variable Expressions
- Alopecia Areata with Renal Dysgenesis
- Moustache restoration using follicular unit extraction technique for esthetic repair of prolabial alopecia in adult male patients with repaired bilateral cleft lip: An initial report in eight patients
- 861 Frontal fibrosing alopecia (FFA) under dynamic optical coherence tomography (D-OCT)
- 864 Catalytic-dependent and -independent activities of Polycomb repressive complex 1 differentially regulate skin stem cell specification
- 865 Conditional ablation of JAK-STAT5 signaling induces anagen hair growth
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- A Clinical Approach to Severe Insulin Resistance
- Phylloid terminal hair nevus: A unique clinical entity
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Cutaneous Drug Reaction Case Reports
- Female Adolescent Hair Disorders
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope