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5. A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI). Pongbangli N; Pitipakorn K; Jai-Aue S; Sirijanchune P; Pongpittayut S; Wongcharoen W Am J Case Rep; 2021 Jan; 22():e928969. PubMed ID: 33414362 [TBL] [Abstract][Full Text] [Related]
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12. Extradural hematoma surgery in a child with Hutchinson-Gilford progeria syndrome: Perioperative concerns. Hansda U; Agarwal J; Patra C; Ganjoo P J Pediatr Neurosci; 2013 May; 8(2):165-7. PubMed ID: 24082942 [TBL] [Abstract][Full Text] [Related]
13. Progeria infantum (Hutchinson-Gilford syndrome) associated with scleroderma-like lesions and acro-osteolysis: a case report and brief review of the literature. Jansen T; Romiti R Pediatr Dermatol; 2000; 17(4):282-5. PubMed ID: 10990576 [TBL] [Abstract][Full Text] [Related]
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15. [Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature]. Huang S; Liang Y; Wu W; Fu X; Liao L; Luo X Zhonghua Er Ke Za Zhi; 2014 Feb; 52(2):112-6. PubMed ID: 24739722 [TBL] [Abstract][Full Text] [Related]
16. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress. Paradisi M; McClintock D; Boguslavsky RL; Pedicelli C; Worman HJ; Djabali K BMC Cell Biol; 2005 Jun; 6():27. PubMed ID: 15982412 [TBL] [Abstract][Full Text] [Related]
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20. Hutchinson-gilford progeria syndrome: a rare genetic disorder. Panigrahi RG; Panigrahi A; Vijayakumar P; Choudhury P; Bhuyan SK; Bhuyan R; Maragathavalli G; Pati AR Case Rep Dent; 2013; 2013():631378. PubMed ID: 24288630 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]