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Journal articles
0
0
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Al-Waili, Khalid.
Oman Medical Specialty Board.
2013-01
Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure.
Journal articles
0
0
Autosomal dominant polycystic kidney disease and pericardial effusion.
Fernandez, Guillermo Alberto Perez.
Oman Medical Specialty Board.
2018-09
Autosomal dominant polycystic kidney disease and pericardial effusion.
Theses and Dissertations
0
0
Determination of LDL cholesterol polygenic score in patients with Familial Hypercholesterolemia
Rahhal, Nour Al Huda
Sultan Qaboos University
2018
Determination of LDL cholesterol polygenic score in patients with Familial Hypercholesterolemia
Journal articles
0
0
Sanjad-Sakati Syndrome in Omani children.
Rafique, Bushra.
Oman Medical Specialty Board.
2010-07
Sanjad-Sakati Syndrome in Omani children.
Journal articles
0
0
Hypercholesterolemia among apparently healthy university students.
Shawar, Said M.
Oman Medical Specialty Board.
2012-07
Hypercholesterolemia among apparently healthy university students.
Journal articles
0
0
Criteria for diagnosis of familial hypercholesterolemia : a comprehensive analysis of the different guidelines, appraising their suitability in the Omani Arab population.
Al-Rasadi, Khalid.
Oman Medical Specialty Board.
2014-03
Criteria for diagnosis of familial hypercholesterolemia : a comprehensive analysis of the different guidelines, appraising their suitability in the Omani Arab population.
Journal articles
0
0
Clinical and genetic characteristics of familial hypercholesterolemia at Sultan Qaboos University Hospital in Oman.
Al-Waili, Khalid.
Oman Medical Specialty Board.
2020-05
Clinical and genetic characteristics of familial hypercholesterolemia at Sultan Qaboos University Hospital in Oman.
Theses and Dissertations
0
0
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Basak, Saroma.
Sultan Qaboos University
2016
Genomic studies of autosomal recessive epilepsies in three Omani consanguineous families
Journal articles
0
0
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
Alafifi, Tariq.
Oman Medical Specialty Board.
2020-05
A novel mutation of PARK-2 gene in a patient with early-onset Parkinson's disease.
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English
(9)
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Journal articles
(7)
Theses and Dissertations
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Journal articles
(7)
Theses and Dissertations
(2)
Subject
Hypercholesterolemia
(3)
Acute coronary syndrome
(1)
Arabs
(1)
Autosomal dominant hypercholesterolemia
(1)
Autosomal recessive disorder
(1)
Autosomal recessive epilepsies
(1)
Autosomal recessive Parkinsonism
(1)
biochemistry
(1)
Biochemistry and molecular biology
(1)
Cardiovascular abnormalities
(1)
Cascade-screening
(1)
Chronic renal diseases
(1)
Codon, Nonsense
(1)
Codon, Terminator
(1)
Coronary heart disease
(1)
Diabetes mellitus
(1)
Dutch criteria
(1)
Familial hypercholesterolemia
(1)
Genomics
(1)
hsCRP
(1)
Molecular biology
(1)
Mutation
(1)
Oman
(1)
Omani consanguineous families
(1)
PARK 2 protein, Human
(1)
Parkinson's disease
(1)
PCSK9 protien
(1)
Pericardial effusion
(1)
Polycystic kidney, Autosomal dominant
(1)
Population--Oman
(1)
Sanjad Sakati syndrome
(1)
Simon-Broome criteria
(1)
University students
(1)
US-Medped criteria
(1)
Author
Al-Waili, Khalid.
(2)
Al-Rasadi, Khalid.
(1)
Alafifi, Tariq.
(1)
Basak, Saroma.
(1)
Fernandez, Guillermo Alberto Perez.
(1)
Rafique, Bushra.
(1)
Rahhal, Nour Al Huda
(1)
Shawar, Said M.
(1)
Publisher
Oman Medical Specialty Board
(7)
Sultan Qaboos University
(2)
sfy39587stp18
