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Research 31–60 of 48
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Subject Index
- Congenital atrichia associated with situs inversus and mesocardia
- Molecular Genetics of Human Hair Diseases
- Eyebrow Loss
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- CAQ Corner: Basic concepts of transplant immunology
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Effect of iron-deficiency anemia on the outcomes of pregnancy, labor, and newborn health
- Epidermal Notch1 recruits innate lymphoid cells to orchestrate normal skin repair
- A Subset of TREM2+ Dermal Macrophages Secretes Oncostatin M to Maintain Hair Follicle Stem Cell Quiescence and Inhibit Hair Growth
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Quality of life in Romanian patients with schizophrenia based on gender, type of schizophrenia, therapeutic approach, and family history
- Dual drug co-encapsulation into liposomes and liposome-derived nanosystems for improved synergistic treatment of skin diseases
- Transethosomes: A Comprehensive Review of Ultra-Deformable Vesicular Systems for Enhanced Transdermal Drug Delivery
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Clouston syndrome associated with eccrine syringofibroadenoma
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Clouston’s Syndrome-A Case Report
- Clouston’s syndrome: a rare case report
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Painful thickened skin on the soles of the feet
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses