Título: Do you know this syndrome? Berardinelli–Seip syndrome

Autor: Machado et al.

Link: http://dx.doi.org/10.1590/abd1806-4841.20132178

Título: Bezafibrato em lactente portador de lipodistrofia generalizada congênita e hipertrigliceridemia grave

Autor: Araújo, Ramos, Borges

Link: https://doi.org/10.1590/S0004-27302013000800012

Título: A new seipin-assoated neurodegenerative syndrome

Autor: Guillén-Navarro et al.

Link: https://pubmed.ncbi.nlm.nih.gov/23564749/

Título: A New Method for Body Fat Evaluation, Body Adiposity Index, Is Useful in Women With Familial Partial Lipodystrophy

Autor: Godoy-Matos et al.

Link: https://onlinelibrary.wiley.com/doi/10.1038/oby.2011.343

Título: Phenotypic diversity in patients with lipodystrophy associated with LMNA mutations

Autor: Mory et al

Link: https://academic.oup.com/ejendo/article-abstract/167/3/423/6659589?redirectedFrom=fulltext&login=false

Título: Body composition study by dual-energy x-ray absorptiometry in familial partial lipodystrophy: finding new tools for an objective evaluation

Autor: Valerio et al.

Link: https://dmsjournal.biomedcentral.com/articles/10.1186/1758-5996-4-40

Título: Body fat distribution in women with familial partial lipodystrophy caused by mutation in the lamin A/C gene

Autor: Monteiro et al

Link: https://journals.lww.com/indjem/fulltext/2012/16010/body_fat_distribution_in_women_with_familial.21.aspx

Título: Kinetics of zinc status and zinc deficiency in Berardinelli-Seip syndrome

Autor: Santos et al.

Link: dx.doi.org/10.1016/j.jtemb.2011.11.002

Título: Association of PPAR-gamma2 polymorphism on lipid profile in berardinelli-seip syndrome

Autor: Baracho et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L70948814

Título: Prevalence of berardinelli-seip syndrome in the Northeast Brazil: A molecular approach

Autor: Medeiros et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L71191697

Título: Serum retinol binding protein 4 is not decreased in congenital generalized lipodystrophy: a case series

Autor: Godoy-Matos et al.

Link: https://doi.org/10.1590/s0004-27302011000400007

Título: Síndrome de Berardinelli- Seip: descrição genética e metabólica de cinco pacientes

Autor: Barra et al.

Link: https://doi.org/10.1590/S0004-27302011000100007

Título: Síndrome de Berardinelli-Seip: descrição genética e metabólica de cinco pacientes

Autor: Barra et al.

Link: https://doi.org/10.1590/S0004-27302011000100007

Título: Do You Know This Syndrome?

Autor: Santos et al.

Link: https://www.scielo.br/j/abd/a/NNhd5VxZxXB9yzTcNv448pJ/?format=pdf&lang=en

Título: Effect of Diet Intervention and Oral ZincSupplementation on Metabolic Control in Berardinelli-Seip Syndrome

Autor: Rocha et al.

Link: https://doi.org/10.1159/000313932

Título: Cardiometabolic Abnormalities in Patients with Berardinelli-Seip Syndrome

Autor: Rêgo et al.

Link: https://doi.org/10.1590/s0066-782x2010000100017

Título: Bone mineral density in berardinelli-seip congenital lipodystrophy

Autor: Oliveira-Filho, Medeiros, Nunes

Link: https://www.embase.com/records?subaction=viewrecord&rid=7&page=1&id=L70225845

Título: Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli–Seip congenital generalized lipodystrophy syndrome

Autor: Miranda et al.

Link: https://doi.org/10.1111/j.1365-2265.2009.03532.x

Título: Autonomic modulation in patients with congenital generalized lipodystrophy (Berardinelli-Seip syndrome)

Autor: Faria et al.

Link: https://doi.org/10.1093/europace/eup095

Título: Autonomic modulation in patients with congenital generalized lipodystrophy (Berardinelli-Seip syndrome)

Autor: Faria et al.

Link: https://doi.org/10.1093/europace/eup095

Título: Metabolic syndrome, an important issue in patients with congenital generalized lipodystrophy

Autor: Rego et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=2&page=1&id=L70355661

Título: Atypical Generalized Lipoatrophy and Severe Insulin Resistance due to a Heterozygous LMNA p.T10I Mutation

Autor: Mory et al.

Link: https://doi.org/10.1590/s0004-27302008000800008

Título: Berardinelli syndrome. A case report with fatal outcom

Autor: Daher et al.

Link: http://ve.scielo.org/scielo.php?script=sci_arttext&pid=S0535-51332008000200011

Título: Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy

Autor: Kim et al.

Link: https://doi.org/10.1210/jc.2007-1328

Título: Association of a Homozygous Nonsense Caveolin-1 Mutation with Berardinelli-Seip Congenital Lipodystrophy

Autor: Kim et al.

Link: https://doi.org/10.1210/jc.2007-1328