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Lipodystrophy
Chapter 7: Monogenic Forms of Diabetes
Lipodystrophy Due to Adipose Tissue Specific Insulin Receptor
Commonly Used Lipidcentric ICD-10 (ICD-9) Codes
Phenotypic and Clinical Outcome Studies in Amyloidosis and Associated Autoinflammatory Diseases
A Case Report of a Chinese Familial Partial Lipodystrophic Patient with Lamin A/C Gene R482Q Mutation and Polycystic Ovary Syndr
Familial Partial Lipodystrophy
A Clinical Guide to Autoinflammatory Diseases: Familial Mediterranean Fever and Next-Of-Kin Seza Ozen and Yelda Bilginer
Hypercholesterolaemia and Its Management Deepak Bhatnagar,1,2 Handrean Soran,1 Paul N Durrington1
Treatment of Nonalcoholic Steatohepatitis in Adults: Present and Future
A Randomized, Double Blind, Placebo-Controlled Study to Assess
Congenital Generalized Lipodystrophy
PCSK9 Inhibitors Provided By: National Lipid Association’S Therapeutics Committee
Downloads/Advisorycommittees/Committeesmeetingmaterials/Drugs/ Sharing Her Pictures
Generalized Lipodystrophy (GL): Triglyceride Levels
Do You Know This Syndrome?* Você Conhece Esta Síndrome?
Acquired: Partial Lipodystrophy (Barraquer-Simons Syndrome) The
Clinical and Research Learnings from a Hybrid, Targeted Sequencing Panel for Dyslipidemias Jacqueline S
Generalized Lipodystrophy (AGL; Lawrence Syndrome)
Top View
Acquired Partial Lipodystrophy (APL) Or Barraquer-Simons Syndrome Is a Rare Form of Progressive Lipodystrophy of Unknown Etiology
Berardinelli-Seip Congenital Lipodystrophy
Fatty Liver in Lipodystrophy: a Review with a Focus on Therapeutic Perspectives of Adiponectin And/Or Leptin Replacement
Congenital Generalized Lipodystrophies—New Insights Into
HIV–ASSOCIATED LIPODYSTROPHY: Pathogenesis, Prognosis, Treatment, and Controversies
Congenital Generalized (CGL; Berardinelli-Seip Syndrome)
1 Non-Alcoholic Steatohepatitis – Diagnostic
Barraquer–Simons Syndrome: a Rare Form of Acquired Lipodystrophy Joana Oliveira1,2* , Paula Freitas1,2, Eva Lau1,2 and Davide Carvalho1,2
Supplementary Materials Table S1. List of 63 Evaluated Genes Related to Dyslipidemia and Premature Atherosclerosis with Associated Phenotypes
The Diagnosis and Management of Lipodystrophy Syndromes: a Multi-Society Practice Guideline
Screening for Familial Hypercholesterolemia
Panniculitis in Children
Membranous Lipodystrophy: Case Report and Review of the Literature*
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
Novel Forms of Lipodystrophy Why Should We Care?
Lipoatrophic Panniculitis Case Report and Review of the Literature
Lipodystrophy Syndrome Vijayanandh Mani
Early Prevention of Atherosclerosis: Detection and Management of Hypercholesterolaemia in Children and Adolescents
Management of Hypertriglyceridemia BMJ: First Published As 10.1136/Bmj.M3109 on 12 October 2020
The Diagnosis and Management of Lipodystrophy Syndromes: a Multi-Society Practice Guideline
Barraquer-Simons Syndrome Occurred After Pregnancy: a Rare Case Report
Acquired Generalized Lipodystrophy
Download Gene List
Prevalence and Incidence of Rare Diseases
What Lipodystrophies Teach Us About the Metabolic Syndrome
Early Detection of Familial Hypercholesterolemia in Children
REVIEW Lipodystrophy
Congenital Generalized Lipodystrophy: a Multisystemic Metabolic Disorder
Review Article Treatment of Nonalcoholic Steatohepatitis in Adults: Present and Future
AKCEA-ANGPTL3-Lrx) Administered Subcutaneously to Subjects with Familial Partial Lipodystrophy
TITLE of CASE Lipotransfer Provides Effective Soft