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Review

The epidemiology of premature aging and associated comorbidities

Pages 1023-1032 | Published online: 05 Aug 2013

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Fabio Coppedè. (2021) Mutations Involved in Premature-Ageing Syndromes. The Application of Clinical Genetics 14, pages 279-295.
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Harry Pachajoa, Angelica Claros-Hulbert, Ximena García-Quintero, Lina Perafan, Andres Ramirez & Andres F Zea-Vera. (2020) Hutchinson–Gilford Progeria Syndrome: Clinical and Molecular Characterization. The Application of Clinical Genetics 13, pages 159-164.
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Josef Dolejs & Petra Marešová. (2017) Onset of mortality increase with age and age trajectories of mortality from all diseases in the four Nordic countries. Clinical Interventions in Aging 12, pages 161-173.
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Articles from other publishers (24)

Theodore C. Goldsmith. (2023) Mammal Aging is Controlled by an Evolvability-Based Adaptive Program. Biochemistry (Moscow) 87:12-13, pages 1405-1412.
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Hisaya Kato & Yoshiro Maezawa. (2022) Atherosclerosis and Cardiovascular Diseases in Progeroid Syndromes. Journal of Atherosclerosis and Thrombosis 29:4, pages 439-447.
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Lucie AumailleyMichel Lebel. (2021) The Impact of Vitamin C on Different System Models of Werner Syndrome. Antioxidants & Redox Signaling 34:11, pages 856-874.
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Katsuhiro Hayashi, Norio Yamamoto, Akihiko Takeuchi, Shinji Miwa, Kentaro Igarashi, Yoshihiro Araki, Hirotaka Yonezawa, Sei Morinaga, Yohei Asano & Hiroyuki Tsuchiya. (2021) Long-term survival in a patient with Hutchinson-Gilford progeria syndrome and osteosarcoma: A case report. World Journal of Clinical Cases 9:4, pages 854-863.
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Valentina Terenzi, Andrea Battisti, Marco Della Monaca, Paolo Priore, Edoardo Brauner, Silvia Mezi, Francesca De Felice, Daniela Musio, Vincenzo Tombolini, Antonella Polimeni & Valentino Valentini. (2021) Management of a rare case of squamous cell carcinoma of the tongue in a patient affected by progeria. Oral Oncology 113, pages 105032.
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C. Lyons, D. Gallagher, T. McSwiney, E. McElnea & F. Kinsella. (2018) The ophthalmic diagnosis and management of four siblings with Werner syndrome. International Ophthalmology 39:6, pages 1371-1378.
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Iván Méndez-López, Idoia Blanco-Luquin, Javier Sánchez-Ruiz de Gordoa, Amaya Urdánoz-Casado, Miren Roldán, Blanca Acha, Carmen Echavarri, Victoria Zelaya, Ivonne Jericó & Maite Mendioroz. (2019) Hippocampal LMNA Gene Expression is Increased in Late-Stage Alzheimer’s Disease. International Journal of Molecular Sciences 20:4, pages 878.
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Chin Wai Hui, Marie-Kim St-Pierre, Jérôme Detuncq, Lucie Aumailley, Marie-Julie Dubois, Vanessa Couture, Daniel Skuk, André Marette, Jacques P. Tremblay, Michel Lebel & Marie-Ève Tremblay. (2018) Nonfunctional mutant Wrn protein leads to neurological deficits, neuronal stress, microglial alteration, and immune imbalance in a mouse model of Werner syndrome. Brain, Behavior, and Immunity 73, pages 450-469.
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Pier Carmine Passarelli, Guido Pasquantonio, Paolo Francesco Manicone, Loredana Cerroni, Roberta Condo’, Manuele Mancini & Antonio D’Addona. (2018) Orofacial signs and dental abnormalities in patients with Mulvihill–Smith syndrome. Medicine 97:18, pages e0656.
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Claudio Franceschi, Paolo Garagnani, Cristina Morsiani, Maria Conte, Aurelia Santoro, Andrea Grignolio, Daniela Monti, Miriam Capri & Stefano Salvioli. (2018) The Continuum of Aging and Age-Related Diseases: Common Mechanisms but Different Rates. Frontiers in Medicine 5.
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Michel Lebel & F. Brad Johnson. (2018) What have we learned so far on the molecular pathogenesis of Werner syndrome using mutant mouse models of this human progeroid disorder?. Drug Discovery Today: Disease Models 27, pages 31-42.
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Fabio Coppedè. 2018. Conn's Handbook of Models for Human Aging. Conn's Handbook of Models for Human Aging 21 34 .
T. Guastafierro, M. G. Bacalini, A. Marcoccia, D. Gentilini, S. Pisoni, A. M. Di Blasio, A. Corsi, C. Franceschi, D. Raimondo, A. Spanò, P. Garagnani & F. Bondanini. (2017) Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome. Clinical Epigenetics 9:1.
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Aoife Doherty, Yelena Kernogitski, Alexander M. Kulminski & João Pedro de Magalhães. (2017) Identification of polymorphisms in cancer patients that differentially affect survival with age. Aging 9:10, pages 2117-2136.
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C. Miaskowski, B.A. Cooper, B. Aouizerat, M. Melisko, L.-M. Chen, L. Dunn, X. Hu, K.M. Kober, J. Mastick, J.D. Levine, M. Hammer, F. Wright, J. Harris, J. Armes, E. Furlong, P. Fox, E. Ream, R. Maguire & N. Kearney. (2017) The symptom phenotype of oncology outpatients remains relatively stable from prior to through 1 week following chemotherapy. European Journal of Cancer Care 26:3, pages e12437.
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Özlem Bilgiç. (2017) Do you know this syndrome? Werner syndrome. Anais Brasileiros de Dermatologia 92:2, pages 271-272.
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Shailima Rampogu, Ayoung Baek, Minky Son, Amir Zeb, Chanin Park, Raj Kumar, Gihwan Lee, Donghwan Kim, Yeonuk Choi, Yeongrae Cho, Yohan Park, Seok Ju Park & Keun Woo Lee. (2017) Computational Exploration for Lead Compounds That Can Reverse the Nuclear Morphology in Progeria. BioMed Research International 2017, pages 1-15.
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Sebastiaan J.M. Vreeswijk, Hedi L. Claahsen, Wilfred A. Borstlap & Mark P. Hendriks. (2016) Anaesthesia and orphan disease. European Journal of Anaesthesiology 33:11, pages 869-872.
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Hideharu Hagiya, Misa Hayashi, Ichiro Katayama & Kazunori Tomono. (2016) Olecranon Osteomyelitis Caused by <i>Mycobacterium chelonae</i>. Internal Medicine 55:13, pages 1825-1825.
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Fabio Coppedè. 2016. Encyclopedia of Endocrine Diseases. Encyclopedia of Endocrine Diseases 669 674 .
H. G. StratmannH. G. Stratmann. 2016. Using Medicine in Science Fiction. Using Medicine in Science Fiction 281 320 .
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