Search
for
Sort by
Research 361–390 of 699
- Aldesleukin
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Hypersensitivity Diseases
- Subject Index
- Index
- Tufted Folikülit: Bir Olgu Sunumu
- Nonscarring Alopecias
- Table of Contents
- British Society for Dermatopathology
- SUMMARIES OF PAPERS
- Main Plenary Sessions: Summaries of Papers
- CME examination for volume 43
- Eye and skin disease
- Dermatologic therapy: December 1987 to December 1988
- Westwood Carolina Conference on Clinical Dermatology
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- MOST IMPORTANT SKIN DISEASES OF CHILDRENTheir Diagnosis and Treatment
- Biology and Genetics of Hair
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Non‐infective mucocutaneous presentations of human immunodeficiency virus infection
- VINCENT BARRANCO, M.D., EDITOR 2121 EAST 21ST STREET, P.O. BOX 52588 TUESA, OK 74152-0588.
- Differential diagnosis of alopetia in children and adolescents
- Pediatric Inpatients Requesting Dermatology Consultation in a Tertiary Care Hospital: Retrospective Analysis of 614 Patients
- Feline Dermatology
- General Dermatology
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Recurrent pruritic polymorphic lesions associated with weight loss
- Oxidative Stress in Alopecia Areata: A Case–Control Study
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis