Search
forResearch 10 of 22
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Hutchinson-Gilford progeria syndrome - A brief introduction
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Premature aging syndromes: From patients to mechanism
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Progeroide Syndrome
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →