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Journal of General Internal Medicine
|
July 18, 2014
Application of a policy framework for the public funding of drugs for rare diseases
Eric Winquist, Doug Coyle, Joe T R Clarke, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 9, 2002
Phenylalanine requirement in children with classical PKU determined by indicator amino acid oxidation
Glenda Courtney-Martin, Rachelle Bross, Mahroukh Raffi, et al.
Journal of Medical Genetics
|
May 29, 2009
Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome Survey
A Mehta, J T R Clarke, R Giugliani, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
February 19, 2004
Total branched-chain amino acids requirement in patients with maple syrup urine disease by use of indicator amino acid oxidation with L-[1-13C]phenylalanine
Roya Riazi, Mahroukh Rafii, Joe T R Clarke, et al.
Molecular Genetics and Metabolism
|
May 12, 2009
Gb(3)/creatinine biomarkers for Fabry disease: issues to consider
Christiane Auray-Blais, David S Millington, Caroline Barr, et al.
The West Indian Medical Journal
|
April 24, 2014
A review of the HIV-infected homeless sub-population at the Centre for HIV/AIDS Research, Education and Services, Department of Medicine, University Hospital of the West Indies
G Barrow, N Clare-Pascoe, A Bahadur, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2003
Clinical and genetic aspects of trigonocephaly: a study of 25 cases
Cyrus Azimi, Shelley J Kennedy, David Chitayat, et al.
Molecular Genetics and Metabolism Reports
|
October 5, 2016
Methylmalonyl-coA epimerase deficiency: A new case, with an acute metabolic presentation and an intronic splicing mutation in the <i>MCEE</i> gene
Paula J Waters, Fanny Thuriot, Joe T R Clarke, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
July 20, 2007
Left ventricular aneurysm in a patient with mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): clinical and pathological correlation
Gavin Y Oudit, Jagdish Butany, William G Williams, et al.
Analytical Biochemistry
|
July 16, 2008
Cryptic splice site in the complementary DNA of glucocerebrosidase causes inefficient expression
Scott W Bukovac, Richard D Bagshaw, Brigitte A Rigat, et al.
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of 12
Search research articles
Search
Showing results (61-70 of 119) with videos related to
Sort By:
Page
of 12
Journal of General Internal Medicine
|
July 18, 2014
Application of a policy framework for the public funding of drugs for rare diseases
Eric Winquist, Doug Coyle, Joe T R Clarke, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 9, 2002
Phenylalanine requirement in children with classical PKU determined by indicator amino acid oxidation
Glenda Courtney-Martin, Rachelle Bross, Mahroukh Raffi, et al.
Journal of Medical Genetics
|
May 29, 2009
Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome Survey
A Mehta, J T R Clarke, R Giugliani, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
February 19, 2004
Total branched-chain amino acids requirement in patients with maple syrup urine disease by use of indicator amino acid oxidation with L-[1-13C]phenylalanine
Roya Riazi, Mahroukh Rafii, Joe T R Clarke, et al.
Molecular Genetics and Metabolism
|
May 12, 2009
Gb(3)/creatinine biomarkers for Fabry disease: issues to consider
Christiane Auray-Blais, David S Millington, Caroline Barr, et al.
The West Indian Medical Journal
|
April 24, 2014
A review of the HIV-infected homeless sub-population at the Centre for HIV/AIDS Research, Education and Services, Department of Medicine, University Hospital of the West Indies
G Barrow, N Clare-Pascoe, A Bahadur, et al.
American Journal of Medical Genetics. Part A
|
February 5, 2003
Clinical and genetic aspects of trigonocephaly: a study of 25 cases
Cyrus Azimi, Shelley J Kennedy, David Chitayat, et al.
Molecular Genetics and Metabolism Reports
|
October 5, 2016
Methylmalonyl-coA epimerase deficiency: A new case, with an acute metabolic presentation and an intronic splicing mutation in the <i>MCEE</i> gene
Paula J Waters, Fanny Thuriot, Joe T R Clarke, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology
|
July 20, 2007
Left ventricular aneurysm in a patient with mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): clinical and pathological correlation
Gavin Y Oudit, Jagdish Butany, William G Williams, et al.
Analytical Biochemistry
|
July 16, 2008
Cryptic splice site in the complementary DNA of glucocerebrosidase causes inefficient expression
Scott W Bukovac, Richard D Bagshaw, Brigitte A Rigat, et al.
Page
of 12