Search research articles
Contact Us
Filters
Showing results (21-30 of 54) with videos related to
Page
of 6
Sort By:
Annals of the Academy of Medicine, Singapore
|
April 1, 1987
Renal transplantation in primary hyperoxaluria
R W Watts, S H Morgan, M A Mansell, et al.
Nephron
|
January 1, 1987
Oxalate dynamics in chronic renal failure. Comparison with normal subjects and patients with primary hyperoxaluria
S H Morgan, P Purkiss, R W Watts, et al.
The British Journal of Radiology
|
January 1, 1985
Pulmonary artery aneurysms in Behçet's disease
R N Gibson, S H Morgan, T Krausz, et al.
Lancet (London, England)
|
November 12, 1983
Anti-Ro antibodies and abortions in women with SLE
R G Hull, E N Harris, S H Morgan, et al.
Annals of the Rheumatic Diseases
|
June 1, 1988
A double blind, placebo controlled trial of intravenous methylprednisolone in systemic lupus erythematosus
C G Mackworth-Young, J David, S H Morgan, et al.
British Journal of Rheumatology
|
November 1, 1984
Sjögren's syndrome presenting as a severe sensory neuropathy including involvement of the trigeminal nerve
R G Hull, S H Morgan, A E Harding, et al.
Human Genetics
|
November 1, 1987
Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88
K D MacDermot, S H Morgan, J K Cheshire, et al.
Nephron
|
January 1, 1990
Exclusion of primary hyperoxaluria type I (PHI) in end-stage renal failure by enzymatic analysis of a percutaneous hepatic biopsy
S H Morgan, C J Danpure, M R Bending, et al.
Contributions to Nephrology
|
January 1, 1984
Effects of acetate or bicarbonate haemodialysis on cardiocirculatory function and acid-base balance
M A Mansell, S H Morgan, C Kong, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 1987
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes
S H Morgan, J K Cheshire, T M Wilson, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 54) with videos related to
Sort By:
Page
of 6
Annals of the Academy of Medicine, Singapore
|
April 1, 1987
Renal transplantation in primary hyperoxaluria
R W Watts, S H Morgan, M A Mansell, et al.
Nephron
|
January 1, 1987
Oxalate dynamics in chronic renal failure. Comparison with normal subjects and patients with primary hyperoxaluria
S H Morgan, P Purkiss, R W Watts, et al.
The British Journal of Radiology
|
January 1, 1985
Pulmonary artery aneurysms in Behçet's disease
R N Gibson, S H Morgan, T Krausz, et al.
Lancet (London, England)
|
November 12, 1983
Anti-Ro antibodies and abortions in women with SLE
R G Hull, E N Harris, S H Morgan, et al.
Annals of the Rheumatic Diseases
|
June 1, 1988
A double blind, placebo controlled trial of intravenous methylprednisolone in systemic lupus erythematosus
C G Mackworth-Young, J David, S H Morgan, et al.
British Journal of Rheumatology
|
November 1, 1984
Sjögren's syndrome presenting as a severe sensory neuropathy including involvement of the trigeminal nerve
R G Hull, S H Morgan, A E Harding, et al.
Human Genetics
|
November 1, 1987
Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88
K D MacDermot, S H Morgan, J K Cheshire, et al.
Nephron
|
January 1, 1990
Exclusion of primary hyperoxaluria type I (PHI) in end-stage renal failure by enzymatic analysis of a percutaneous hepatic biopsy
S H Morgan, C J Danpure, M R Bending, et al.
Contributions to Nephrology
|
January 1, 1984
Effects of acetate or bicarbonate haemodialysis on cardiocirculatory function and acid-base balance
M A Mansell, S H Morgan, C Kong, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 1987
Anderson-Fabry disease--family linkage studies using two polymorphic X-linked DNA probes
S H Morgan, J K Cheshire, T M Wilson, et al.
Page
of 6