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Korabiusz Katarzyna, Wawryków Agata. Causes of lipodystrophy. Journal of Education, Health and Sport. 2018;8(9):1765-1770. eISNN 2391-8306. DOI http://dx.doi.org/10.5281/zenodo.1410147 http://ojs.ukw.edu.pl/index.php/johs/article/view/5921 https://pbn.nauka.gov.pl/sedno-webapp/works/876219 The journal has had 7 points in Ministry of ...
Katarzyna Korabiusz, Agata Wawryków
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European lipodystrophy registry: background and structure [PDF]
Background Lipodystrophy syndromes comprise a group of extremely rare and heterogeneous diseases characterized by a selective loss of adipose tissue in the absence of nutritional deprivation or catabolic state. Because of the rarity of each lipodystrophy
Julia von Schnurbein +24 more
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Lipodystrophy : focus on HIV Lipodystrophy [PDF]
Lipodystrophy is a rare condition which can be inherited or acquired, localised or generalised. It is characterised by abnormal adipose tissue distribution and in some cases underlying metabolic derangement, including diabetes mellitus, hypertriglyceridemia, hepatic steatosis, polycystic ovaries and acanthosis nigricans.
Giordano Imbroll, Miriam +2 more
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Recent developments in lipodystrophy
Purpose of review Lipodystrophy syndromes have an estimated prevalence of 1.3–4.7 cases per million and as with other rare diseases conducting research can be challenging. The present review highlights recently published work that has provided insights into the field of non-HIV--associated lipodystrophy syndromes.
Melvin, Audrey +2 more
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Biological Depiction of Lipodystrophy and Its Associated Challenges Among HIV AIDS Patients: Literature Review [PDF]
Tolera Ambisa Lamesa School of Medical Laboratory Science, Jimma University, Jimma, EthiopiaCorrespondence: Tolera Ambisa Lamesa, Email toleraambisa@gmail.comAbstract: Lipodystrophy syndrome is a medical condition characterized by the absence of adipose ...
Lamesa TA
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Respiratory chain dysfunction associated with multiple mitochondrial DNA deletions in antiretroviral therapy-related lipodystrophy. [PDF]
Highly-active antiretroviral therapy (HAART) can induce a characteristic lipodystrophy syndrome characterized by peripheral fat wasting and central adiposity, usually associated with hyperlipidaemia and insulin resistance [1,2].
Cardellach, Francesc +5 more
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Genetic basis of Asian diabetes. [PDF]
ABSTRACT Recent genomic studies in Asian populations have advanced our understanding of the diagnosis, pathophysiology, risk prediction, and precision care of diabetes. Monogenic diabetes, including maturity‐onset diabetes of the young (MODY) and mitochondrial diabetes, highlights the importance of genetic diagnosis for subtype‐specific care.
Ojima T, Yamauchi T.
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Lipodystrophy and adipose tissue recovery are mediated by the Wnt/lipogenesis axis during skin fibrosis. [PDF]
Abstract Acquired lipodystrophy in the dermal white adipose tissue (DWAT) is an early phenotype of skin fibrosis, followed by the accumulation of extracellular matrix (ECM). Lipodystrophy syndromes are estimated to affect 1 in 20,000 people and are associated with metabolic comorbidities.
Madhavan SR +10 more
europepmc +2 more sources
RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease
RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease. Abstract Background and Aims Receptor‐interacting protein kinase 3 (RIPK3) mediates NAFLD progression, but its metabolic function is unclear. Here, we aimed to investigate the role of RIPK3 in modulating mitochondria function, coupled with lipid droplet (LD)
Marta B. Afonso +16 more
wiley +1 more source
Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy
Background/Aims: Lipodystrophy is a rare metabolic disorder characterized by near total or partial lack of subcutaneous adipose tissue and associated with insulin resistance.
Canan Altay +15 more
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