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D J Carson

Showing results (31-40 of 63) with videos related to

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The Ulster Medical Journal|October 1, 1987
Renal tubular acidosis with nerve deafnessM A McShane, D J Carson, A O Redmond, et al.
Irish Journal of Medical Science|September 1, 1982
Screening for congenital hypothyroidism in Northern IrelandD J Carson, G Roberts, S L Campbell, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Pediatric Radiology|January 1, 1990
Osteopenia and phenylketonuriaD J Carson, L G Greeves, L E Sweeney, et al.
Gut|July 1, 1981
Changes in N-terminal glucagon-like immunoreactivity and insulin during short-term gluten challenge in childhood coeliac diseaseD J Carson, J F Glasgow, K D Buchanan, et al.
Archives of Disease in Childhood|February 1, 1986
Congenital hypothyroidism missed on screeningG A Grant, D J Carson, M M Reid, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
European Journal of Pediatrics|July 1, 1990
Neuroblastoma in a patient with dihydropteridine reductase deficiencyL G Greeves, R J Leeming, K Hyland, et al.
The Journal of Pediatrics|June 4, 1999
Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndromeJ M Kirk, C E Brain, D J Carson, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Ulster Medical Journal|October 1, 1987
Renal tubular acidosis with nerve deafnessM A McShane, D J Carson, A O Redmond, et al.
Irish Journal of Medical Science|September 1, 1982
Screening for congenital hypothyroidism in Northern IrelandD J Carson, G Roberts, S L Campbell, et al.
American Journal of Human Genetics|December 1, 1995
Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approachJ Zschocke, C A Graham, D J Carson, et al.
Pediatric Radiology|January 1, 1990
Osteopenia and phenylketonuriaD J Carson, L G Greeves, L E Sweeney, et al.
Gut|July 1, 1981
Changes in N-terminal glucagon-like immunoreactivity and insulin during short-term gluten challenge in childhood coeliac diseaseD J Carson, J F Glasgow, K D Buchanan, et al.
Archives of Disease in Childhood|February 1, 1986
Congenital hypothyroidism missed on screeningG A Grant, D J Carson, M M Reid, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemiaJ Zschocke, C A Graham, F J Stewart, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
European Journal of Pediatrics|July 1, 1990
Neuroblastoma in a patient with dihydropteridine reductase deficiencyL G Greeves, R J Leeming, K Hyland, et al.
The Journal of Pediatrics|June 4, 1999
Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndromeJ M Kirk, C E Brain, D J Carson, et al.
Pageof 7