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- Progeroide Syndrome
- BG02 A case of Werner syndrome: undiagnosed progeroid syndrome presenting as female pattern hair loss
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- 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
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.
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