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Research 571–600 of 1000+
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- Penis Endocrinology
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Non-classical Congenital Adrenal Hyperplasia Presenting With Severe Androgenic Alopecia: A Case Report
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Hair shaft disorders
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Oral Manifestations of Hematologic and Nutritional Diseases
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Abstracts Pt.30
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Hair and Nail Relationship
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report