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Research 61–90 of 64
- Trichoscopic Signs in Dermatomyositis, Systemic Lupus Erythematosus, and Systemic Sclerosis: A Comparative Study of 150 Patients
- Mechanisms of autophagy and their implications in dermatological disorders
- Clinical Characterization and Treatment Response of Folliculitis Decalvans Lichen Planopilaris Phenotypic Spectrum: A Unicentre Retrospective Series of 31 Patients
- Scalp Micropigmentation
- Scleroderma and L-tryptophan: A possible explanation of the eosinophilia-myalgia syndrome
- Dermal Mucinosis in the Eosinophilia-Myalgia Syndrome
- Cutaneous Mucinosis in a Patient With Eosinophilia-Myalgia Syndrome Associated With L-Tryptophan Ingestion
- Lipodermatosclerosis: a postphiebitic syndrome
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- The eosinophilia-myalgia syndrome
- How to diagnose a lipodystrophy syndrome
- Comparison of the Pathology of Fascia in Eosinophilic Myalgia Syndrome Patients and Idiopathic Eosinophilic Fasciitis
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Werner′s syndrome
- Endocrine-skin interactions
- Male fertility and skin diseases
- Werner's syndrome: incidental finding during pregnancy
- Neuroendokrine paraneoplastische Syndrome
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Eosinophilic Fasciitis Associated With Tryptophan Ingestion
- American Academy of Dermatology
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Cutaneous manifestations of endocrine diseases in children
- Myotonic Dystrophy—A Progeroid Disease?
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers