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Research 31–60 of 1000+
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- The human hair: from anatomy to physiology
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Disorders of Hair Growth: Diagnosis and Treatment
- Cutaneous melanoma, prostate-specific antigen testing and the subsequent risk of prostate cancer diagnosis: a prospective analysis of the 45 and Up Study
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Revolutionizing psoriasis care: Microneedle innovations in treatment and diagnosis
- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children
- Transcriptional Profiling in Rat Hair Follicles following Simulated Blast Insult: A New Diagnostic Tool for Traumatic Brain Injury
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Recent advances in understanding and managing male infertility
- Emerging Diagnostic and Therapeutic Potentials of Human Hair Proteomics
- The Molecular Basis of Blood Diseases
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Adult Male Hypogonadism: A Laboratory Medicine Perspective on Its Diagnosis and Management
- The use of auto-antibody testing in the evaluation of interstitial lung disease (ILD) – A practical approach for the pulmonologist
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Generalised cutaneous necrosis: a complication of low-molecular-weight heparin
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ichthyosis with confetti: clinics, molecular genetics and management
- Parasitic dermatitis in dogs: A literature review of clinical and diagnostic aspects and treatment approaches
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Adverse Reactions to Biologic Medications Used in Allergy and Immunology Diseases
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load