Recent Publications on Hypobetalipoproteinemia: |  |
[Clinical and genetic heterogeneity in hypobetalipoproteinemia]
Familial hypobetalipoproteinemia (FHBL) is one of the causes of...
Direct Link | 1st October, 2009
|
|
[Familial hypobetalipoproteinemia: clinical characterization of a new mutation in the APOB gene]
BACKGROUND AND OBJETIVE: Familial hypobetalipoproteinemia (FHB) is usually...
Direct Link | 1st October, 2009
| Servicio de Endocrinologia, Hospital General, Segovia, Espana.
|
Apolipoprotein B gene mutations and fatty liver in Japanese hypobetalipoproteinemia.
BACKGROUND: Familial hypobetalipoproteinemia (FHBL) is a hereditary...
Direct Link | 25th September, 2009
| Department of Internal Medicine, Graduate School of Medical Science,
|
Familial hypobetalipoproteinemia: early neurological, hematological, and ocular manifestations in two affected twins responding to vitamin supplementation.
Familial hypobetalipoproteinemia is a disorder of lipid metabolism...
Direct Link | 24th September, 2009
| aDepartments of Pediatric Medicine, Rheumatology, and Child
|
PCSK9 Dominant Negative Mutant Results in Increased LDL Catabolic Rate and Familial Hypobetalipoproteinemia.
OBJECTIVE: Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a...
Direct Link | 19th September, 2009
| IRT-UN l'institut du Thorax LI7R415. 8, Quai Moncousu BP70721, 44007
|
Recurrent familial hypobetalipoproteinemia-induced nonalcoholic fatty liver disease after living donor liver transplantation.
Familial hypobetalipoproteinemia (FHBL) is one of the causes of...
Direct Link | 11th September, 2009
| Department of Surgery and Medical Science, Graduate School of Medical
|
Cryptogenic cirrhosis in a patient with familial hypocholesterolemia due to a new truncated form of apolipoprotein B.
Familial hypobetalipoproteinemia (FHBL) is an autosomal codominantly...
Direct Link | 10th September, 2009
| Functional Unit of Biochemistry of Metabolic Diseases, Laboratory of
|
Do diabetes and obesity promote hepatic fibrosis in familial heterozygous hypobetalipoproteinemia?
BACKGROUND: Familial hypobetalipoproteinemia (FHBL) is a hereditary...
Direct Link | 4th August, 2009
|
|
Mutations and polymorphisms in the proprotein convertase subtilisin kexin 9 (PCSK9) gene in cholesterol metabolism and disease.
Hypercholesterolemia is one of the major causes of coronary heart disease...
Direct Link | 7th July, 2009
| Institut Nationale de la Sante et de la Recherche Medicale (INSERM), U781,
|
Dysmorphic findings in two cases of abeta/hypobetalipoproteinemia.
OBJECTIVE: Familial hypobetalipoproteinemia (FHBL) is characterized by...
Direct Link | 29th May, 2009
| Medical Genetics Branch, National Human Genome Research Institute,
|
Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia.
OBJECTIVE: Familial hypobetalipoproteinemia (FHBL) is characterized by...
Direct Link | 7th April, 2009
| Department of Clinical Medicine and Emerging Diseases, University of
|
Identification of patients with abetalipoproteinemia and homozygous familial hypobetalipoproteinemia in Tunisia.
BACKGROUND: Abetalipoproteinemia (ABL) and Homozygous Familial...
Direct Link | 13th March, 2009
| Research Unit of Genetic and Biologic Factors of Atherosclerosis, Faculty
|
Functional analysis of two novel splice site mutations of APOB gene in familial hypobetalipoproteinemia.
Familial hypobetalipoproteinemia (FHBL) is a co-dominant disorder...
Direct Link | 3rd March, 2009
| Department of Biomedical Sciences, University of Modena and Reggio Emilia,
|
| Fatty liver and insulin resistance: not always linked.
| 14th November, 2008
| Washington University School of Medicine, Department of Internal Medicine,
|
| [Neuroacanthocytosis update]
| 13th August, 2008
| Department of Psychiatry, Kagoshima University Graduate School of Medical
|
