Works matching Progeria
Results: 896
Ocular manifestations in the Hutchinson-Gilford progeria syndrome.
- Published in:
- Indian Journal of Ophthalmology, 2011, v. 59, n. 6, p. 509, doi. 10.4103/0301-4738.86327
- By:
- Publication type:
- Article
Anesthetic management of a patient with Progeria.
- Published in:
- International Student Journal of Nurse Anesthesia, 2011, v. 10, n. 2, p. 43
- By:
- Publication type:
- Article
Small-Molecule Therapeutic Perspectives for the Treatment of Progeria.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 7190, doi. 10.3390/ijms22137190
- By:
- Publication type:
- Article
Anesthetic considerations in children with Hutchinson‐Gilford progeria syndrome: A narrative review.
- Published in:
- Pediatric Anesthesia, 2020, v. 30, n. 5, p. 537, doi. 10.1111/pan.13847
- By:
- Publication type:
- Article
Cancer Drug and Progeria.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 294, n. 16, p. 2016, doi. 10.1001/jama.294.16.2016-a
- By:
- Publication type:
- Article
Progeria: A brief review.
- Published in:
- International Journal of Pharmacy & Life Sciences, 2013, v. 4, n. 9, p. 2965
- By:
- Publication type:
- Article
Hutchinson-Gilford progeria syndrome: a rare case report.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
Hutchinson–Gilford Progeria Syndrome: Clinical and Molecular Characterization.
- Published in:
- Application of Clinical Genetics, 2020, v. 13, p. 159, doi. 10.2147/TACG.S238715
- By:
- Publication type:
- Article
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment.
- Published in:
- Cellular & Molecular Life Sciences, 2005, v. 62, n. 22, p. 2669, doi. 10.1007/s00018-005-5318-6
- By:
- Publication type:
- Article
Involvement of xeroderma pigmentosum group A (XPA) in progeria arising from defective maturation of prelamin A.
- Published in:
- FASEB Journal, 2008, v. 22, n. 2, p. 603, doi. 10.1096/fj.07-8598com
- By:
- Publication type:
- Article
Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient.
- Published in:
- 2023
- By:
- Publication type:
- Case Study
Detection of Cerebrovascular Disease in a Child with Hutchinson-Gilford Progeria Syndrome Using MR Angiography: A Case Report.
- Published in:
- Journal of the Korean Society of Radiology (2951-0805), 2022, v. 83, n. 6, p. 1360, doi. 10.3348/jksr.2022.0051
- By:
- Publication type:
- Article
Progeria and Aging—Omics Based Comparative Analysis.
- Published in:
- Biomedicines, 2022, v. 10, n. 10, p. N.PAG, doi. 10.3390/biomedicines10102440
- By:
- Publication type:
- Article
Progeria—a Rare Genetic Condition with Accelerated Ageing Process.
- Published in:
- Applied Biochemistry & Biotechnology, 2023, v. 195, n. 4, p. 2587, doi. 10.1007/s12010-021-03514-y
- By:
- Publication type:
- Article
Aortic Calcification in a Patient With Hutchinson–Gilford Progeria Syndrome.
- Published in:
- Pediatric Cardiology, 2010, v. 31, n. 6, p. 925, doi. 10.1007/s00246-010-9711-z
- By:
- Publication type:
- Article
Mechanisms of A-Type Lamin Targeting to Nuclear Ruptures Are Disrupted in LMNA- and BANF1- Associated Progerias.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 5, p. 865, doi. 10.3390/cells11050865
- By:
- Publication type:
- Article
The Molecular and Cellular Basis of Hutchinson–Gilford Progeria Syndrome and Potential Treatments.
- Published in:
- Genes, 2023, v. 14, n. 3, p. 602, doi. 10.3390/genes14030602
- By:
- Publication type:
- Article
Gene-rich chromosomal regions are preferentially localized in the lamin B deficient nuclear blebs of atypical progeria cells.
- Published in:
- Nucleus (1949-1034), 2015, v. 6, n. 1, p. 66, doi. 10.1080/19491034.2015.1004256
- By:
- Publication type:
- Article
Progeria: report of a case and review of the literature.
- Published in:
- 1991
- By:
- Publication type:
- journal article
Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.
- Published in:
- European Heart Journal, 2021, v. 42, n. 42, p. 4352, doi. 10.1093/eurheartj/ehab547
- By:
- Publication type:
- Article
A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndrome.
- Published in:
- Pediatric Radiology, 2012, v. 42, n. 9, p. 1089, doi. 10.1007/s00247-012-2423-1
- By:
- Publication type:
- Article
Sex-specific preservation of neuromuscular function and metabolism following systemic transplantation of multipotent adult stem cells in a murine model of progeria.
- Published in:
- GeroScience, 2024, v. 46, n. 1, p. 1285, doi. 10.1007/s11357-023-00892-5
- By:
- Publication type:
- Article
Pharmacotherapy to gene editing: potential therapeutic approaches for Hutchinson–Gilford progeria syndrome.
- Published in:
- GeroScience, 2020, v. 42, n. 2, p. 467, doi. 10.1007/s11357-020-00167-3
- By:
- Publication type:
- Article
Microbiome at sites of gingival recession in children with Hutchinson-Gilford progeria syndrome.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Extradural hematoma surgery in a child with Hutchinson--Gilford progeria syndrome: Perioperative concerns.
- Published in:
- Journal of Pediatric Neurosciences, 2013, v. 8, n. 2, p. 165, doi. 10.4103/1817-1745.117860
- By:
- Publication type:
- Article
Hutchinson-Gilford progeria syndrome.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T.
- Published in:
- Cell & Tissue Research, 2023, v. 394, n. 1, p. 189, doi. 10.1007/s00441-023-03813-2
- By:
- Publication type:
- Article
Premature ageing in children: a rare genetic disorder called progeria.
- Published in:
- International Journal of Pharmaceutical Research (09752366), 2020, v. 12, n. 3, p. 31, doi. 10.31838/ijpr/2020.12.03.005
- By:
- Publication type:
- Article
Early Onset Diabetes in Two Children due to Progeria, a Monogenic Disease of DNA Repair.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 315, doi. 10.4274/jcrpe.galenos.2019.2019.0126
- By:
- Publication type:
- Article
Progeria: an extremely unusual disorder.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Hutchinson–Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.
- Published in:
- British Journal of Dermatology, 2007, v. 156, n. 6, p. 1308, doi. 10.1111/j.1365-2133.2007.07897.x
- By:
- Publication type:
- Article
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).
- Published in:
- American Journal of Case Reports, 2021, p. 1, doi. 10.12659/AJCR.928969
- By:
- Publication type:
- Article
Aging Model for Analyzing Drug-Induced Proarrhythmia Risks Using Cardiomyocytes Differentiated from Progeria-Patient-Derived Induced Pluripotent Stem Cells.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 15, p. 11959, doi. 10.3390/ijms241511959
- By:
- Publication type:
- Article
Non-syndromic cardiac progeria in a patient with the rare pathogenic p.Asp300Asn variant in the LMNA gene.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Progeria: A rare genetic premature ageing disorder.
- Published in:
- Indian Journal of Medical Research, 2014, v. 139, n. 5, p. 667
- By:
- Publication type:
- Article
Simultaneous Shoulder and Hip Dislocation in a 12-Year-Old Girl with Hutchinson-Gilford Progeria Syndrome.
- Published in:
- Acta Medica Iranica, 2012, v. 50, n. 6, p. 439
- By:
- Publication type:
- Article
Molecular elucidations of hutchinson-gilford progeria syndrome: A hope for managing horrors of premature aging in children.
- Published in:
- Pakistan Journal of Pharmaceutical Sciences, 2020, v. 33, n. 3, p. 1179, doi. 10.36721/PJPS.2020.33.3.REG.1179-1182.1
- By:
- Publication type:
- Article
Acute Coronary Syndrome Treated with Percutaneous Coronary Intervention in Hutchinson–Gilford Progeria.
- Published in:
- Children, 2023, v. 10, n. 3, p. 526, doi. 10.3390/children10030526
- By:
- Publication type:
- Article
Characterization of the craniofacial abnormalities of the homozygous G608G progeria mouse model.
- Published in:
- Frontiers in Physiology, 2024, p. 1, doi. 10.3389/fphys.2024.1481985
- By:
- Publication type:
- Article
Treatment Considerations in Hutchinson-Gilford Progeria Syndrome: A Case Report.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Néstor-Guillermo Progeria Syndrome: a biochemical insight into Barrier-to-Autointegration Factor 1, alanine 12 threonine mutation.
- Published in:
- BMC Molecular Biology, 2014, v. 15, n. 1, p. 1, doi. 10.1186/s12867-014-0027-z
- By:
- Publication type:
- Article
Modelling premature cardiac aging with induced pluripotent stem cells from a hutchinson-gilford Progeria Syndrome patient.
- Published in:
- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.1007418
- By:
- Publication type:
- Article
An Analysis of Hearing Outcomes in Children with Hutchinson-Gilford Progeria Syndrome.
- Published in:
- British Journal of Hospital Medicine (17508460), 2024, v. 85, n. 11, p. 1, doi. 10.12968/hmed.2024.0449
- By:
- Publication type:
- Article
Molecular insights into the premature aging disease progeria.
- Published in:
- Histochemistry & Cell Biology, 2016, v. 145, n. 4, p. 401, doi. 10.1007/s00418-016-1411-1
- By:
- Publication type:
- Article
Paclitaxel mitigates structural alterations and cardiac conduction system defects in a mouse model of Hutchinson–Gilford progeria syndrome.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 2, p. 503, doi. 10.1093/cvr/cvab055
- By:
- Publication type:
- Article
Hutchinson-Gilford Progeria Syndrome: Its Presentation in F. Scott Fitzgerald's Short Story 'The Curious Case of Benjamin Button' and Its Oral Manifestations.
- Published in:
- Journal of Dental Research, 2009, v. 88, n. 10, p. 873, doi. 10.1177/0022034509348765
- By:
- Publication type:
- Article
Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 10, p. 1350, doi. 10.3390/cells12101350
- By:
- Publication type:
- Article
Progerinin, an Inhibitor of Progerin, Alleviates Cardiac Abnormalities in a Model Mouse of Hutchinson–Gilford Progeria Syndrome.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 9, p. 1232, doi. 10.3390/cells12091232
- By:
- Publication type:
- Article
Rescue of Mitochondrial Function in Hutchinson-Gilford Progeria Syndrome by the Pharmacological Modulation of Exportin CRM1.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 2, p. 275, doi. 10.3390/cells12020275
- By:
- Publication type:
- Article
Establishment and Characterization of hTERT Immortalized Hutchinson–Gilford Progeria Fibroblast Cell Lines.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 18, p. N.PAG, doi. 10.3390/cells11182784
- By:
- Publication type:
- Article