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Quoted phrase not found in phrase index: "CIDEC-related familial partial lipodystrophy"
Page 1
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. The most common forms are the familial partial lipodystrophy (FPLD) syndromes, which include a set of disorders, usually autosomal dominant, due to diffe …
Lipodystrophies are a heterogeneous group of rare conditions characterised by the loss of adipose tissue. The most common forms are the f …
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 …
Lipodystrophic laminopathies: Diagnostic clues.
Guillín-Amarelle C, Fernández-Pombo A, Sánchez-Iglesias S, Araújo-Vilar D. Guillín-Amarelle C, et al. Nucleus. 2018 Jan 1;9(1):249-260. doi: 10.1080/19491034.2018.1454167. Nucleus. 2018. PMID: 29557732 Free PMC article. Review.
Those disorders in which adipose tissue is affected are called laminopathic lipodystrophies and include type 2 familial partial lipodystrophy and certain premature aging syndromes. ...
Those disorders in which adipose tissue is affected are called laminopathic lipodystrophies and include type 2 familial partial …
Adipokines and aging.
Arai Y, Takayama M, Abe Y, Hirose N. Arai Y, et al. J Atheroscler Thromb. 2011;18(7):545-50. doi: 10.5551/jat.7039. Epub 2011 May 7. J Atheroscler Thromb. 2011. PMID: 21551960 Free article. Review.
However, adipokine dysregulation is paradoxically associated with lipodystrophy and lipoatrophy with aging. In familial partial lipodystrophic syndromes and Hutchinson-Gilford progeria syndrome, both of which are caused by mutations in the LMNA gene, loss of …
However, adipokine dysregulation is paradoxically associated with lipodystrophy and lipoatrophy with aging. In familial par …
C3 nephritic factors: A changing landscape.
Levy Erez D, Meyers KE, Sullivan KE. Levy Erez D, et al. J Allergy Clin Immunol. 2017 Jul;140(1):57-59. doi: 10.1016/j.jaci.2017.02.018. Epub 2017 Mar 16. J Allergy Clin Immunol. 2017. PMID: 28322851 Free PMC article. No abstract available.
Impaired Muscle Mitochondrial Function in Familial Partial Lipodystrophy.
Simha V, Lanza IR, Dasari S, Klaus KA, Le Brasseur N, Vuckovic I, Laurenti MC, Cobelli C, Port JD, Nair KS. Simha V, et al. J Clin Endocrinol Metab. 2022 Jan 18;107(2):346-362. doi: 10.1210/clinem/dgab725. J Clin Endocrinol Metab. 2022. PMID: 34614176 Free PMC article.
CONTEXT: Familial partial lipodystrophy (FPL), Dunnigan variety is characterized by skeletal muscle hypertrophy and insulin resistance besides fat loss from the extremities. ...
CONTEXT: Familial partial lipodystrophy (FPL), Dunnigan variety is characterized by skeletal muscle hypertrophy and ins …
Lipodystrophies.
Garg A. Garg A. Am J Med. 2000 Feb;108(2):143-52. doi: 10.1016/s0002-9343(99)00414-3. Am J Med. 2000. PMID: 11126308 Review.
The lipodystrophies can be classified into two major types: familial and acquired. The main subtypes of familial lipodystrophies are congenital generalized lipodystrophy, an autosomal recessive disorder characterized by near complete lack of metabolically act …
The lipodystrophies can be classified into two major types: familial and acquired. The main subtypes of familial lipodystrophi …
How to diagnose a lipodystrophy syndrome.
Vantyghem MC, Balavoine AS, Douillard C, Defrance F, Dieudonne L, Mouton F, Lemaire C, Bertrand-Escouflaire N, Bourdelle-Hego MF, Devemy F, Evrard A, Gheerbrand D, Girardot C, Gumuche S, Hober C, Topolinski H, Lamblin B, Mycinski B, Ryndak A, Karrouz W, Duvivier E, Merlen E, Cortet C, Weill J, Lacroix D, Wémeau JL. Vantyghem MC, et al. Ann Endocrinol (Paris). 2012 Jun;73(3):170-89. doi: 10.1016/j.ando.2012.04.010. Epub 2012 Jun 28. Ann Endocrinol (Paris). 2012. PMID: 22748602 Review.
Lipodystrophy refers to a group of rare diseases characterized by the generalized or partial absence of adipose tissue, and occurs with or without hypertrophy of adipose tissue in other sites. They are classified as being familial or acquired, and generalized …
Lipodystrophy refers to a group of rare diseases characterized by the generalized or partial absence of adipose tissue, and oc …
Clinical Features and Management of Non-HIV-Related Lipodystrophy in Children: A Systematic Review.
Gupta N, Asi N, Farah W, Almasri J, Barrionuevo P, Alsawas M, Wang Z, Haymond MW, Brown RJ, Murad MH. Gupta N, et al. J Clin Endocrinol Metab. 2017 Feb 1;102(2):363-374. doi: 10.1210/jc.2016-2271. J Clin Endocrinol Metab. 2017. PMID: 27967300 Free PMC article. Review.
CONTEXT: Lipodystrophy syndromes are characterized by generalized or partial absence of adipose tissue. ...Generalized fat loss involving face, neck, abdomen, thorax, and upper and lower limbs was explicitly reported in 65% to 93% of patients with congenital general …
CONTEXT: Lipodystrophy syndromes are characterized by generalized or partial absence of adipose tissue. ...Generalized fat los …
Pelvis Magnetic Resonance Imaging to Diagnose Familial Partial Lipodystrophy.
Adiyaman SC, Altay C, Kamisli BY, Avci ER, Basara I, Simsir IY, Atik T, Secil M, Oral EA, Akinci B. Adiyaman SC, et al. J Clin Endocrinol Metab. 2023 Jul 14;108(8):e512-e520. doi: 10.1210/clinem/dgad063. J Clin Endocrinol Metab. 2023. PMID: 36808247
CONTEXT: The diagnosis of familial partial lipodystrophy (FPLD) is currently made based on clinical judgment. ...When this approach was tested in a larger dataset of random patients, FPLD was differentiated from subjects without lipodystrophy with 96.6 …
CONTEXT: The diagnosis of familial partial lipodystrophy (FPLD) is currently made based on clinical judgment. ...When t …
120 results