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The Medical Journal of Australia
|
May 1, 1976
Management of phenylketonuria: South Australian experience of 13 cases
E F Robertson, G N Hill, K Cashel, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiency
G K Brown, R D Scholem, S M Hunt, et al.
The Medical Journal of Australia
|
May 2, 1981
Combined analysis of acetylcholinesterase and alpha-fetoprotein improves the accuracy of antenatal diagnosis of neural-tube defects
A J Hodgson, P M Pilowsky, E F Robertson, et al.
Clinical and Experimental Neurology
|
January 1, 1985
Phytanic acid oxidase deficiency in childhood
G A Wise, B J Duffy, J D Mitchell, et al.
Developmental Medicine and Child Neurology
|
February 1, 1989
A child with Refsum's disease: successful treatment with diet and plasma exchange
N Dickson, J G Mortimer, J M Faed, et al.
The Medical Journal of Australia
|
October 11, 1975
Bioavailability of phenytoin from various pharmaceutical preparations in children
J I Manson, S M Beal, A Magarey, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher disease in the dog
B R Farrow, W J Hartley, A C Pollard, et al.
The Medical Journal of Australia
|
March 20, 1982
Enzymatic diagnosis of the mucopolysaccharidoses: experience of 96 cases diagnosed in a five-year period
J J Hopwood, V Muller, J R Harrison, et al.
The Medical Journal of Australia
|
February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight years
W F Carey, J J Hopwood, A Poulos, et al.
Archives of Disease in Childhood
|
July 1, 1978
Successful restoration of immunity in the DiGeorge syndrome with fetal thymic epithelial transplant
Y H Thong, E F Robertson, H G Rischbieth, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 52) with videos related to
Sort By:
Page
of 6
The Medical Journal of Australia
|
May 1, 1976
Management of phenylketonuria: South Australian experience of 13 cases
E F Robertson, G N Hill, K Cashel, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiency
G K Brown, R D Scholem, S M Hunt, et al.
The Medical Journal of Australia
|
May 2, 1981
Combined analysis of acetylcholinesterase and alpha-fetoprotein improves the accuracy of antenatal diagnosis of neural-tube defects
A J Hodgson, P M Pilowsky, E F Robertson, et al.
Clinical and Experimental Neurology
|
January 1, 1985
Phytanic acid oxidase deficiency in childhood
G A Wise, B J Duffy, J D Mitchell, et al.
Developmental Medicine and Child Neurology
|
February 1, 1989
A child with Refsum's disease: successful treatment with diet and plasma exchange
N Dickson, J G Mortimer, J M Faed, et al.
The Medical Journal of Australia
|
October 11, 1975
Bioavailability of phenytoin from various pharmaceutical preparations in children
J I Manson, S M Beal, A Magarey, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher disease in the dog
B R Farrow, W J Hartley, A C Pollard, et al.
The Medical Journal of Australia
|
March 20, 1982
Enzymatic diagnosis of the mucopolysaccharidoses: experience of 96 cases diagnosed in a five-year period
J J Hopwood, V Muller, J R Harrison, et al.
The Medical Journal of Australia
|
February 18, 1984
Prenatal diagnosis of lysosomal storage diseases. Review of experience in 145 patient referrals over a period of eight years
W F Carey, J J Hopwood, A Poulos, et al.
Archives of Disease in Childhood
|
July 1, 1978
Successful restoration of immunity in the DiGeorge syndrome with fetal thymic epithelial transplant
Y H Thong, E F Robertson, H G Rischbieth, et al.
Page
of 6