Physician

Internal Medicine

Dr. Silvia S. Fojo, MD

Silvia S. Fojo, MD practices Internal Medicine. Dr. Silvia S. Fojo is a published doctor as well. She has 29 publications published. The latest was: Absence of triglyceride accumulation in lipoprotein lipase-deficient human monocyte-macrophages incubated with human very low density lipoprotein.

Publications

An ATP-binding cassette gene (ABCG5) from the ABCG (White) gene subfamily maps to human chromosome 2p21 in the region of the Sitosterolemia locus.
Homozygous hypobetalipoproteinemia: transcriptional regulation and 5''-flanking sequence analysis in an apolipoprotein B deficiency state.
An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-II.
A nonsense mutation in the apolipoprotein C-IIPadova gene in a patient with apolipoprotein C-II deficiency.
The molecular biology of human apoA-I, apoA-II, apoC-II and apoB.
Lipoprotein lipaseBethesda: a single amino acid substitution (Ala-176----Thr) leads to abnormal heparin binding and loss of enzymic activity.
Molecular genetics of apoC-II and lipoprotein lipase deficiency.
Identification of two separate allelic mutations in the lipoprotein lipase gene of a patient with the familial hyperchylomicronemia syndrome.
Hypertriglyceridaemia due to genetic defects in lipoprotein lipase and apolipoprotein C-II.
The molecular defects in lipoprotein lipase deficient patients.
Apolipoprotein C-II deficiency syndrome due to apo C-IIHamburg: clinical and biochemical features and HphI restriction enzyme polymorphism.
Purification and characterization of a colony stimulating factor from human lung.
The isolation and characterization of a colony stimulating factor from human lung.
Absence of triglyceride accumulation in lipoprotein lipase-deficient human monocyte-macrophages incubated with human very low density lipoprotein.
A naturally occurring mutation at the second base of codon asparagine 43 in the proposed N-linked glycosylation site of human lipoprotein lipase: in vivo evidence that...
Human apolipoprotein C-II: complete nucleic acid sequence of preapolipoprotein C-II.
Analysis of the apoC-II gene in apoC-II deficient patients.
The localization of the gene for apolipoprotein C-II to chromosome 19.
Human preproapolipoprotein C-II. Analysis of major plasma isoforms.
Effectiveness of mevinolin on plasma lipoprotein concentrations in type II hyperlipoproteinemia.
Apolipoprotein C-II deficiency: identification of a structural variant ApoC-II Padova.
Identification of an apoC-II variant (apoC-IIBethesda) in a kindred with apoC-II deficiency and type I hyperlipoproteinemia.
Translational and post-translational processing in apolipoprotein metabolism.
Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiency.
A deletion mutation in the ApoC-II gene (ApoC-II Nijmegen) of a patient with a deficiency of apolipoprotein C-II.
Apolipoproteins and lipoproteins in human plasma: an overview.
The human preproapolipoprotein C-II gene. Complete nucleic acid sequence and genomic organization.
Adrenocortical function in type II hyperlipoproteinemic patients treated with lovastatin (mevinolin).

Schools

Washington Center School of Medicine

Doctors Specialties

Internal Medicine

Accepted Insurances

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