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Lipomatosis
Genetic Determinants Underlying Rare Diseases Identified Using Next-Generation Sequencing Technologies
Unilateral Multiple Tuberous Xanthomas Mimicking Multiple Lipomatosis in Type Iia Hypercholesterolemia- a Case Report with Review
Lipoprotein Lipase: a General Review Moacir Couto De Andrade Júnior1,2*
Difference Between Dyslipidemia and Hyperlipidemia Key Difference – Dyslipidemia Vs Hyperlipidemia
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Sequence Diversity in Genes of Lipid Metabolism Christine Kim Garcia,1 Gabriele Mues,2 Yuanlan Liao,1 Tommy Hyatt,1 Nila Patil,3 Jonathan C
A Case of Symmetrical Lipomatosis of the Tongue Presenting As Macroglossia
Renal Replacement Lipomatosis - a Rare but Also Underdiagnosed Entity
Inhibitors on Lipoprotein Lipase Transcriptase
Clinical and Research Learnings from a Hybrid, Targeted Sequencing Panel for Dyslipidemias Jacqueline S
The Diagnosis and Management of Lipodystrophy Syndromes: a Multi-Society Practice Guideline
United States Patent (19) 11 Patent Number: 6,093,699 Sehon Et Al
Introduction HDL Metabolism
Cutaneous Xanthoma- a Clue to Familial Hypercholesterolemia
A Case of Multiple Lipomas Coexisting with Angiolipomas: Familial Multiple Lipomatosis Or a Distinct Entity? Funda Tamer1, Mehmet Eren Yuksel2
Spinal Epidural Lipomatosis Is Associated with Liver Fat Deposition
EPHX1 Mutations Cause a Lipoatrophic Diabetes Syndrome Due To
The Diagnosis and Management of Lipodystrophy Syndromes: a Multi-Society Practice Guideline
Top View
(001-139) Includes: Diseases Generally Recogniz
Type 2 Benign Symmetric Lipomatosis (Launois-Bensaude)*
Dercum's Disease and Roch-Leri Mesosomatous Lipomatosis
Adult-Onset Asymmetrical Lipomatosis
Supplemental Information
The Morbid Anatomy of the Human Genome: Chromosomal Location of Mutations Causing Disease
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Neurometabolic Disorder with Neuromuscular Manifestation
Dercum's Disease and Roch-Leri Mesosomatic Lipomatosis
Multiple Symmetric Lipomatosis: a Diagnostic Dilemma
Launois-Bensaude Syndrome) – a Rare Cause of Muscular Weakness
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
Carbohydrate and Lipid Disorders and Relevant Considerations in Persons with Spinal Cord Injury
What Lipodystrophies Teach Us About the Metabolic Syndrome
Case Report Familial Abdominal and Intestinal Lipomatosis Presenting with Upper GI Bleeding
Disease ID Disorder Name Gene Symbols OMIM ID