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A C Pollard

Showing results (41-50 of 52) with videos related to

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The Medical Journal of Australia|May 1, 1976
Management of phenylketonuria: South Australian experience of 13 casesE 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 deficiencyG 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 defectsA J Hodgson, P M Pilowsky, E F Robertson, et al.
Clinical and Experimental Neurology|January 1, 1985
Phytanic acid oxidase deficiency in childhoodG 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 exchangeN 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 childrenJ I Manson, S M Beal, A Magarey, et al.
Progress in Clinical and Biological Research|January 1, 1982
Gaucher disease in the dogB 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 periodJ 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 yearsW 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 transplantY H Thong, E F Robertson, H G Rischbieth, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
The Medical Journal of Australia|May 1, 1976
Management of phenylketonuria: South Australian experience of 13 casesE 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 deficiencyG 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 defectsA J Hodgson, P M Pilowsky, E F Robertson, et al.
Clinical and Experimental Neurology|January 1, 1985
Phytanic acid oxidase deficiency in childhoodG 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 exchangeN 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 childrenJ I Manson, S M Beal, A Magarey, et al.
Progress in Clinical and Biological Research|January 1, 1982
Gaucher disease in the dogB 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 periodJ 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 yearsW 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 transplantY H Thong, E F Robertson, H G Rischbieth, et al.
Pageof 6