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Research 391–420 of 1000+
- Ottawa, Ontario, Canada, February 13–16, 2013
- Subject Index
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Common causes of paediatric alopecia
- Mesenchymal Stem Cell Exosomes Therapy for Acquired Trichorrhexis Nodosa: A Case Series
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Patterns of noncicatricial alopecia in children: a cross-sectional study
- Expert consensus recommendations on appropriate serological testing for the chief complaint of alopecia
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Oral Presentations
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- SnapshotDx Quiz: May 2022
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- FOXN1 deficient nude severe combined immunodeficiency
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Alopecia in Belgian Blue crossbred calves: a case series
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Evaluation and Treatment of Hirsutism in Premenopausal Women: An Endocrine Society Clinical Practice Guideline
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype