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A D Patrick

Showing results (31-40 of 53) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1981
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twinsR G Gray, A D Patrick, F E Preston, et al.
The New England Journal of Medicine|March 2, 1978
Expression of hexosaminidase isoenzymes in childhood leukemiaR B Ellis, N T Rapson, A D Patrick, et al.
FEBS Letters|July 15, 1970
Tay-sachs disease and related disorders: Fractionation of brain N-acetyl-beta-hexosaminidase on DEAE-celluloseE P. Young, R B. Ellis, B D. Lake, et al.
Lancet (London, England)|November 17, 1973
Letter: Prenatal diagnosis of Tay-Sachs diseaseR B Ellis, J U Ikonne, A D Patrick, et al.
Pediatrics|September 1, 1972
Leukocyte -galactosidase activity in GM 1 -gangliosidosisE Young, R B Ellis, A D Patrick, et al.
Archives of Disease in Childhood|March 1, 1973
Family with intermittent maple syrup urine diseaseH B Valman, A D Patrick, J W Seakins, et al.
Archives of Disease in Childhood|December 1, 1977
Mannosidosis. Clinical and biochemical studyP J Milla, I E Black, A D Patrick, et al.
Lancet (London, England)|August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiencyC H Rodeck, A D Patrick, M E Pembrey, et al.
The Quarterly Journal of Medicine|January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 casesJ Spencer-Peet, M E Norman, B D Lake, et al.
Prenatal Diagnosis|February 1, 1987
First trimester diagnosis of cystinosis using intact chorionic villiA D Patrick, E P Young, J Mossman, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1981
Acute hereditary tyrosinaemia type I: clinical, biochemical and haematological studies in twinsR G Gray, A D Patrick, F E Preston, et al.
The New England Journal of Medicine|March 2, 1978
Expression of hexosaminidase isoenzymes in childhood leukemiaR B Ellis, N T Rapson, A D Patrick, et al.
FEBS Letters|July 15, 1970
Tay-sachs disease and related disorders: Fractionation of brain N-acetyl-beta-hexosaminidase on DEAE-celluloseE P. Young, R B. Ellis, B D. Lake, et al.
Lancet (London, England)|November 17, 1973
Letter: Prenatal diagnosis of Tay-Sachs diseaseR B Ellis, J U Ikonne, A D Patrick, et al.
Pediatrics|September 1, 1972
Leukocyte -galactosidase activity in GM 1 -gangliosidosisE Young, R B Ellis, A D Patrick, et al.
Archives of Disease in Childhood|March 1, 1973
Family with intermittent maple syrup urine diseaseH B Valman, A D Patrick, J W Seakins, et al.
Archives of Disease in Childhood|December 1, 1977
Mannosidosis. Clinical and biochemical studyP J Milla, I E Black, A D Patrick, et al.
Lancet (London, England)|August 7, 1982
Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiencyC H Rodeck, A D Patrick, M E Pembrey, et al.
The Quarterly Journal of Medicine|January 1, 1971
Hepatic glycogen storage disease. Clinical and laboratory findings in 23 casesJ Spencer-Peet, M E Norman, B D Lake, et al.
Prenatal Diagnosis|February 1, 1987
First trimester diagnosis of cystinosis using intact chorionic villiA D Patrick, E P Young, J Mossman, et al.
Pageof 6