Search
for
Sort by
Research 511–540 of 1000+
- Transfollicular Drug Delivery Systems
- To σύνδρομο της δερματίτιδας από λείξη των άκρων στο σκύλο
- The Case Files
- In the quest to stymie time, will laboratory data stand up in man?
- Diagnosis and therapeutic management of staphylococcal dermatitis in a sheep: A case report
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Folliculitis Decalvans: An Uncommon Case Report with Review of Literature
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- KASUS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA-MITIS YANG TERDIAGNOSIS PADA SAAT LANJUT USIA
- To compare the sensitivity pattern of direct immunofluorescence of perilesional skin and plucked hair in pemphigus vulgaris
- Characterization of an autoimmune condition associated with AEC syndrome
- Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Keratin gene mutations in disorders of human skin and its appendages
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- Disorders of Keratinization
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Profile of tofacitinib citrate and its potential in the treatment of moderate-to-severe chronic plaque psoriasis
- Fabrication and Characterization of Electrospun Membranes Based on “Poly(ε-caprolactone)”, “Poly(3-hydroxybutyrate)” and Their Blend for Tunable Drug Delivery of Curcumin
- Long‐Term Management with Adipose Tissue‐Derived Mesenchymal Stem Cells and Conventional Treatment in a Dog with Hepatocutaneous Syndrome
- Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Severe Ulceronecrotic Dermatitis Associated with Mite Infestation in the Critically Endangered Amargosa Vole (<i>Microtus californicus scirpensis</i>)
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- A trichobezoar in a child with undiagnosed celiac disease: A case report
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Kaposi varicelliform eruption
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis