Título: Glycated Hemoglobin in the Diagnosis of Diabetes Mellitus in a Semi-Urban Brazilian Population

Autor: Moreira et al.

Link: https://www.mdpi.com/1660-4601/16/19/3598

Título: Association between cardiovascular autonomic neuropathy and left ventricular hypertrophy in young patients with congenital generalized lipodystrophy

Autor: Ponte et al.

Link: https://doi.org/10.1186/s13098-019-0444-8

Título: Type 2 Congenital Generalized Lipodystrophy: The Diagnosis is in Your Hands

Autor: Montenegro Júnior et al.

Link: https://doi.org/10.1016/j.jpeds.2018.11.030

Título: Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell Carcinoma

Autor: Falcão et al.

Link: https://doi.org/10.1210/jc.2018-02221

Título: Aggressive papillary thyroid carcinoma in a child with type 2 congenital generalized lipodystrophy

Autor: Lima et al.

Link: https://doi.org/10.20945/2359-3997000000096

Título: Evaluation of the hypothalamic–pituitary–adrenal axis in a case series of familial partial lipodystrophy

Autor: Elias et al.

Link: https://doi.org/10.1186/s13098-018-0396-4

Título: Cardiovascular risk in individuals with congenital generalized lipodystrophy through calcium coronary score

Autor: Feijó et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L629759429

Título: Nutritional status of zinc and magnesium in patients with congenital generalized lipodystrophy

Autor: Lopes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L629760217

Título: Evaluation of Oxidative Stress Markers and their Correlation with Respiratory Muscle Strength in Congenital Generalized Lipodystrophy

Autor: Campos et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L630917843

Título: Evaluation of comorbidities and clinical outcomes of nine patients with lipodystrophy treated in an university hospital

Autor: Oliveira et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L629759758

Título: Pancreatic fat deposition is increased and related to beta cell function in women with familial partial lipodystrophy

Autor: Godoy-Matos et al.

Link: https://doi.org/10.1186/s13098-018-0375-9

Título: Impairment of respiratory muscle strength in Berardinelli-Seip congenital lipodystrophy subjects

Autor: Medeiros et al.

Link: https://doi.org/10.1186/s12931-018-0879-8

Título: Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred

Autor: Montenegro Júnior et al.

Link: https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2018.00458/full

Título: Insulin resistance, cardiovascular autonomic neuropathy, and left ventricular hypertrophy in patients with congenital generalized lipodystrophy

Autor: Fernandes et al.

Link: https://doi.org/10.2337/db18-585-P

Título: Sleep disorders in patients with congenital generalized lipodystrophy

Autor: Fernandes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=3&page=1&id=L623567802

Título: Causes of death in patients with Berardinelli- Seip congenital generalized lipodystrophy

Autor: Lima et al.

Link: https://doi.org/10.1371/journal.pone.0199052

Título: Case Report of Acquired Generalized Lipodystrophy Associated With Common Variable Immunodeficiency

Autor: Halpern, Nery e Pereira

Link: https://doi.org/10.1210/jc.2018-00494

Título: Bone Density in Patients With Berardinelli-Seip Congenital Lipodystrophy Is Higher in Trabecular Sites and in Type 2 Patients

Autor: Lima et al.

Link: https://doi.org/10.1016/j.jocd.2016.10.002

Título: Endoplasmic reticulum stress activation in adipose tissue induces metabolic syndrome in individuals with familial partial lipodystrophy of the Dunnigan type

Autor: Foss-Freitas et al.

Link: https://doi.org/10.1186/s13098-017-0301-6

Título: Experiência de pessoas que vivem com a Síndrome de Berardinelli-Seip no Nordeste brasileiro

Autor: Damasceno et al.

Link: https://doi.org/10.1590/1413-81232018232.16802017

Título: Experience of people living with the Berardinelli-Seip Syndrome in the Brazilian Northeast

Autor: Damasceno et al.

Link: https://doi.org/10.1590/1413-81232018232.16802017

Título: Early commitment of cardiovascular autonomic modulation in Brazilian patients with congenital generalized lipodystrophy

Autor: Ponte et al.

Link: https://doi.org/10.1186/s12872-017-0738-4

Título: SGLT2 inhibitors effect on fatty liver disease in patients with Berardinelli-Seip lipodystrophy

Autor: Parente et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=2&page=1&id=L624031182

Título: Subclinical ventricular dysfunction in young population with congenital generalised lipodystrophy detected by speckle-tracking echocardiography

Autor: Fernandes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L624031894

Título: Evaluation of respiratory muscle strength and balance in Berardinelli-Seip congenital lipodystrophy (BSCL) patients from Brazil

Autor: Campos et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L626625358

Título: Achados oftalmológicos na lipodistrofia generalizada congênita-um possível marcador de distúrbios metabólicos

Autor: Fernandes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L623565822

Título: Diabetes mellitus evolution in two brothers with berardinelli-seip congenital lipodystrophy (BSCL), one R

Autor: Oliveira et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L621966131

Título: Thyroid dysfunction and insulin resistance in patients with congenital generalized lipodystrophy

Autor: Lima et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=10&page=1&id=L621966207

Título: Assessment of food intake of patients with congenital generalized lipodystrophy in relation to the guidelines of brazilian diabetes society

Autor: Albuquerque et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L621966385

Título: High doses of insulin in children with congenital generalized lipodistrophy (CGL) and serious insulin resistance

Autor: Martins et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L621966533

Título: Glucocorticoid sensitivity might underlie metabolic abnormalities in patients with familial partial lipodystrophy type 2

Autor: Resende et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L621966406

Título: DDP4 inhibitor activity in partial family lipodystrophy-case report

Autor: Muto, Pádua

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L621966507

Título: A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p. T10I Mutation

Autor: Hussain et al.

Link: https://pmc.ncbi.nlm.nih.gov/articles/PMC6283411/

Título: High prevalence of Berardinelli Seip Congenital Lipodystrophy in Rio Grande do Norte State, Northeast Brazil

Autor: Medeiros et al.

Link: https://doi.org/10.1186/s13098-017-0280-7

Título: Normal Bone Density and Trabecular Bone Score, but High Serum Sclerostin in Congenital Generalized Lipodystropy

Autor: Lima et al.

Link: https://doi.org/10.1016/j.bone.2017.03.053

Título: Dipeptidyl peptidase-4 levels are increased and partially related to body fat distribution in patients with familial partial lipodystrophy type 2

Autor: Valerio et al.

Link: https://dmsjournal.biomedcentral.com/articles/10.1186/s13098-017-0226-0

Título: Early results of the first Brazilian patients with generalised congenital lipodystrophy on treatment with metreleptin

Autor: Lima et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L618051702

Título: Severe metabolic abnormalities observed in patients with confirmed diagnosis of congenital generalized lipodystrophy including AGPAT2 and BSCL2 mutations

Autor: Montenegro Júnior et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L623677857

Título: Evaluation of the presence of steatosis and fibrosis in lipodystrophic with diabetes type 2 patients using transient elastography and comparison with anthropometric and densitometric parameters

Autor: De Franca et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L618937190

Título: Clinical and laboratory data of a large series of patients with congenital generalized lipodystrophy

Autor: Lima et al.

Link: https://doi.org/10.1186/s13098-016-0140-x

Título: High prevalence of cardiovascular autonomic neuropathy in young patients with congenital generalised lipodystrophy (Berardinelli-Seip Syndrome)

Autor: Ponte et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L612313333

Título: Hepatic elastography, metabolic profile and body composition of four patients with berardinelli-seip lipodystrophy

Autor: Schnoll et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L613519719

Título: Congenital lipoatrophy diabetes syndromes: Basal metabolism and thyroid function

Autor: Filho et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L613523034

Título: Precocious endothelial dysfunction in patients with congenital generalized lipodystrophy evaluated by two different methods

Autor: Fernandes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L620237207

Título: A Novel Syndrome of Generalized Lipodystrophy Associated With Pilocytic Astrocytoma

Autor: Patni et al.

Link: https://pmc.ncbi.nlm.nih.gov/articles/PMC4596037/

Título: Evaluation of epicardial adipose tissue in familial partial lipodystrophy

Autor: Godoy-Matos et al.

Link: https://dmsjournal.biomedcentral.com/articles/10.1186/s13098-015-0024-5

Título: Clinical and laboratory characteristics of 14 patients with Berardinelli-Seip syndrome

Autor: Montenegro Júnior et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=3&page=1&id=L72030936

Título: Evaluation of steatohepatitis, body composition and metabolic profile of three patients with Berardinelli-Seip syndrome

Autor: Schnoll et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L615888307

Título: Detection of congenital generalized lipodystrophy mutations by nextgeneration sequencing: Time for a new approach

Autor: Riquetto et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L615888321

Título: 25Hydroxy-Vitamin D status in patients with berardinelli-seip syndrome (congenital generalized lipodystrophy)

Autor: Karbage et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L615888339

Título: Precocious endothelial dysfunction in patients with congenital generalized lipodystrophy (Berardinelli-Seip syndrome) evaluated by two different methods

Autor: Fernandes et al.

Link: https://www.embase.com/records?subaction=viewrecord&rid=1&page=1&id=L615888356

Título: Association between Pro12Ala, Pvull, Avall, Sstl and ADIPOQ Single-Nucleotide Polymorphisms with Lipid and Glycemic Profiles of Patients with Berardinelli-Seip Syndrome

Autor: Baracho et al.

Link: https://doi.org/10.1159/000366026