Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1927 1
1930 1
1933 1
1934 1
1939 1
1941 1
1945 1
1946 5
1947 7
1948 12
1949 15
1950 14
1951 12
1952 21
1953 25
1954 19
1955 16
1956 13
1957 17
1958 15
1959 24
1960 23
1961 33
1962 19
1963 55
1964 65
1965 37
1966 25
1967 31
1968 27
1969 27
1970 21
1971 29
1972 39
1973 36
1974 38
1975 41
1976 40
1977 35
1978 40
1979 32
1980 31
1981 27
1982 37
1983 31
1984 31
1985 26
1986 22
1987 29
1988 36
1989 31
1990 27
1991 19
1992 24
1993 36
1994 26
1995 27
1996 36
1997 33
1998 77
1999 154
2000 205
2001 240
2002 264
2003 299
2004 278
2005 299
2006 287
2007 315
2008 331
2009 290
2010 260
2011 270
2012 264
2013 275
2014 262
2015 237
2016 257
2017 224
2018 265
2019 254
2020 256
2021 228
2022 249
2023 212
2024 236
2025 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

7,668 results

Results by year

Filters applied: . Clear all
Page 1
Lipodystrophy Syndromes.
Hussain I, Garg A. Hussain I, et al. Endocrinol Metab Clin North Am. 2016 Dec;45(4):783-797. doi: 10.1016/j.ecl.2016.06.012. Epub 2016 Oct 6. Endocrinol Metab Clin North Am. 2016. PMID: 27823605 Free PMC article. Review.
The two most common genetic varieties include congenital generalized lipodystrophy and familial partial lipodystrophy; the two most common acquired varieties include acquired generalized lipodystrophy and acquired partial lipodystrophy. Highly active a …
The two most common genetic varieties include congenital generalized lipodystrophy and familial partial lipodystrophy; the two …
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline.
Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M, Mungai L, Oral EA, Patni N, Rother KI, von Schnurbein J, Sorkina E, Stanley T, Vigouroux C, Wabitsch M, Williams R, Yorifuji T. Brown RJ, et al. J Clin Endocrinol Metab. 2016 Dec;101(12):4500-4511. doi: 10.1210/jc.2016-2466. Epub 2016 Oct 6. J Clin Endocrinol Metab. 2016. PMID: 27710244 Free PMC article. Review.
Patients with most lipodystrophy syndromes should be screened for diabetes, dyslipidemia, and liver, kidney, and heart disease annually. Diet is essential for the management of metabolic complications of lipodystrophy. Metreleptin therapy is effective for metabolic …
Patients with most lipodystrophy syndromes should be screened for diabetes, dyslipidemia, and liver, kidney, and heart disease annual …
Lipodystrophy for the Diabetologist-What to Look For.
Patni N, Garg A. Patni N, et al. Curr Diab Rep. 2022 Sep;22(9):461-470. doi: 10.1007/s11892-022-01485-w. Epub 2022 Jul 11. Curr Diab Rep. 2022. PMID: 35821558 Free PMC article. Review.
In this review, we discuss the various subtypes and when to suspect and how to diagnose lipodystrophy. RECENT FINDINGS: The four major subtypes are autosomal recessive, congenital generalized lipodystrophy (CGL); acquired generalized lipodystrophy (AGL), most …
In this review, we discuss the various subtypes and when to suspect and how to diagnose lipodystrophy. RECENT FINDINGS: The four majo …
Diagnosis and treatment of lipodystrophy: a step-by-step approach.
Araújo-Vilar D, Santini F. Araújo-Vilar D, et al. J Endocrinol Invest. 2019 Jan;42(1):61-73. doi: 10.1007/s40618-018-0887-z. Epub 2018 Apr 27. J Endocrinol Invest. 2019. PMID: 29704234 Free PMC article. Review.
PURPOSE: To describe the clinical presentation of known types of lipodystrophy, and suggest specific steps to recognize, diagnose and treat lipodystrophy in the clinical setting. ...CONCLUSIONS: Here, we describe the clinical presentation of known types of lipody …
PURPOSE: To describe the clinical presentation of known types of lipodystrophy, and suggest specific steps to recognize, diagnose and …
Autoimmunity in lipodystrophy syndromes.
Ceccarini G, Magno S, Gilio D, Pelosini C, Santini F. Ceccarini G, et al. Presse Med. 2021 Nov;50(3):104073. doi: 10.1016/j.lpm.2021.104073. Epub 2021 Sep 20. Presse Med. 2021. PMID: 34547374 Free article. Review.
Based on the evidence of a positive association between most acquired lipodystrophies and autoimmune disorders including immune mediated alterations in the adipose tissue of patients affected by acquired lipodystrophy, a reaction against white adipose tissue antigen …
Based on the evidence of a positive association between most acquired lipodystrophies and autoimmune disorders including immune media …
Recent developments in lipodystrophy.
Melvin A, Stears A, Savage DB. Melvin A, et al. Curr Opin Lipidol. 2019 Aug;30(4):284-290. doi: 10.1097/MOL.0000000000000613. Curr Opin Lipidol. 2019. PMID: 31135595 Review.
The present review highlights recently published work that has provided insights into the field of non-HIV--associated lipodystrophy syndromes. RECENT FINDINGS: Lipodystrophies are a heterogenous group of disorders, as such research is often focused on specific subt …
The present review highlights recently published work that has provided insights into the field of non-HIV--associated lipodystrophy …
Familial partial lipodystrophy syndromes.
Fernández-Pombo A, Sánchez-Iglesias S, Cobelo-Gómez S, Hermida-Ameijeiras Á, Araújo-Vilar D. Fernández-Pombo A, et al. Presse Med. 2021 Nov;50(3):104071. doi: 10.1016/j.lpm.2021.104071. Epub 2021 Oct 2. Presse Med. 2021. PMID: 34610417 Review.
Lipodystrophies are a heterogeneous group of rare conditions characterised by the loss of adipose tissue. ...Although no well-defined diagnostic criteria have been established for lipodystrophy, there are certain clues related to medical history, physical examinatio …
Lipodystrophies are a heterogeneous group of rare conditions characterised by the loss of adipose tissue. ...Although no well-defined …
Molecular and Cellular Bases of Lipodystrophy Syndromes.
Zammouri J, Vatier C, Capel E, Auclair M, Storey-London C, Bismuth E, Mosbah H, Donadille B, Janmaat S, Fève B, Jéru I, Vigouroux C. Zammouri J, et al. Front Endocrinol (Lausanne). 2022 Jan 3;12:803189. doi: 10.3389/fendo.2021.803189. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35046902 Free PMC article. Review.
Lipodystrophy syndromes are rare diseases originating from a generalized or partial loss of adipose tissue. ...After an update on the main molecular bases and clinical forms of lipodystrophy, we will focus on topics that have recently emerged in the field. We will d …
Lipodystrophy syndromes are rare diseases originating from a generalized or partial loss of adipose tissue. ...After an update on the …
Genetics of lipodystrophy syndromes.
Jéru I. Jéru I. Presse Med. 2021 Nov;50(3):104074. doi: 10.1016/j.lpm.2021.104074. Epub 2021 Sep 23. Presse Med. 2021. PMID: 34562561 Review.
The classical forms of LS include partial, generalized, and progeroid lipodystrophies. They are usually due to defects in proteins playing a key role in adipogenesis and adipocyte functions. More recently, systemic disorders combining lipodystrophy and multiple orga …
The classical forms of LS include partial, generalized, and progeroid lipodystrophies. They are usually due to defects in proteins pl …
Partial lipodystrophy: Clinical presentation and treatment.
Mosbah H, Vatier C, Vigouroux C. Mosbah H, et al. Ann Endocrinol (Paris). 2024 Jun;85(3):197-200. doi: 10.1016/j.ando.2024.05.015. Epub 2024 Jun 12. Ann Endocrinol (Paris). 2024. PMID: 38871513 Review.
They are characterized by a lack of adipose tissue or a lack of adipose development leading to metabolic disorders associated with often severe insulin resistance, hypertriglyceridemia and hepatic steatosis. In partial forms of lipodystrophy, these mechanisms are aggravate …
They are characterized by a lack of adipose tissue or a lack of adipose development leading to metabolic disorders associated with often sev …
7,668 results