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Results of search for 'au:"Applegarth, D A"', page 6 of 7
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Authors
Applegarth, D A
Bozoian, G
Bridges, M A
Chitayat, D
Clarke, L A
Coulter-Mackie, M B
Davidson, A G
Dimmick, J E
Dunn, H G
Evans, M E
Farrell, K
Hardwick, D F
Israels, S
Kirby, L T
Levy, H L
Lowry, R B
MacLeod, P M
Ross, P M
Toone, J R
Wong, L T
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Topics
Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Child
Child, Preschool
Cystic Fibrosis
Female
Glycine
Humans
Infant
Infant, Newborn
Male
Pregnancy
analysis
blood
diagnosis
enzymology
genetics
metabolism
urine
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English
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101.
Case report: diagnosis and management of type I hyperlipoproteinemia.
[electronic resource]
by
Ireton, C L
Davidson, A G
Applegarth, D A
Reilander, M A
Israels, S
Producer:
19750329
In:
Journal of the American Dietetic Association
vol. 66
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102.
Isolation of pure, active alpha 2 macroglobulin from small-scale plasma samples.
[electronic resource]
by
Bridges, M A
Applegarth, D A
Johannson, J
Davidson, A G
Wong, L T
Producer:
19820322
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 118
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103.
Protease binding by alpha 2 macroglobulin in cystic fibrosis.
[electronic resource]
by
Bridges, M A
Applegarth, D A
Johannson, J
Wong, L T
Davidson, A G
Producer:
19820322
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 118
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104.
Morquio disease presenting as hydrops fetalis and enzyme analysis of chorionic villus tissue in a subsequent pregnancy.
[electronic resource]
by
Applegarth, D A
Toone, J R
Wilson, R D
Yong, S L
Baldwin, V J
Producer:
19880620
In:
Pediatric pathology
vol. 7
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105.
Conclusions from a pilot immunoreactive trypsin newborn screen for cystic fibrosis.
[electronic resource]
by
Kirby, L T
Davidson, A G
Applegarth, D A
Wong, L T
Hardwick, D F
Producer:
19830909
In:
Clinical chemistry
vol. 29
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106.
Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria.
[electronic resource]
by
Randak, C
Roschinger, W
Rolinski, B
Hadorn, H B
Applegarth, D A
Roscher, A A
Producer:
20010111
In:
Journal of inherited metabolic disease
vol. 23
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107.
Letter: Slide test for alpha-fetoprotein.
[electronic resource]
by
Baird, P A
Applegarth, D A
Lowry, R B
Miller, J R
MacLeod, P M
Producer:
19761029
In:
Canadian Medical Association journal
vol. 115
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108.
Morphological and histochemical changes in intestinal mucosa in the reserpine-treated rat model of cystic fibrosis.
[electronic resource]
by
Park, C M
Reid, P E
Owen, D A
Sanker, J M
Applegarth, D A
Producer:
19870908
In:
Experimental and molecular pathology
vol. 47
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109.
Pathogenesis of methionine-induced toxicity.
[electronic resource]
by
Hardwick, D F
Applegarth, D A
Cockcroft, D M
Ross, P M
Cder, R J
Producer:
19700619
In:
Metabolism: clinical and experimental
vol. 19
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110.
Argininosuccinic aciduria. A developmental and biochemical case study.
[electronic resource]
by
Margalith, D
Crichton, J U
Wong, L
Davidson, A G
Applegarth, D A
Toone, J R
Producer:
19831028
In:
Journal of the neurological sciences
vol. 60
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111.
Comparison of the carbohydrate composition of alpha 2-macroglobulin from patients with cystic fibrosis and normal controls.
[electronic resource]
by
Park, C M
Reid, P E
Applegarth, D A
Wong, L T
MacDonald, I B
Producer:
19850621
In:
Pediatric research
vol. 19
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112.
Guanosine triphosphate cyclohydrolase I deficiency: early diagnosis by routine urine pteridine screening.
[electronic resource]
by
Naylor, E W
Ennis, D
Davidson, A G
Wong, L T
Applegarth, D A
Niederwieser, A
Producer:
19870331
In:
Pediatrics
vol. 79
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113.
Juvenile galactosialidosis in a white male: a new variant.
[electronic resource]
by
Chitayat, D
Applegarth, D A
Lewis, J
Dimmick, J E
McCormick, A Q
Hall, J G
Producer:
19890505
In:
American journal of medical genetics
vol. 31
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114.
Glycogen storage disease type I: effect of continuous nocturnal nasogastric feeding.
[electronic resource]
by
Davidson, A G
Wong, L T
Kirby, L
Tze, W J
Rigg, J M
Applegarth, D A
Producer:
19790313
In:
Monographs in human genetics
vol. 9
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115.
The differential diagnosis of adult onset metachromatic leukodystrophy and early onset familial Alzheimer disease in an Alzheimer clinic population.
[electronic resource]
by
Sadovnick, A D
Tuokko, H
Applegarth, D A
Toone, J R
Hadjistavropoulos, T
Beattie, B L
Producer:
19940322
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 20
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116.
Biochemical investigation of a child with molybdenum cofactor deficiency.
[electronic resource]
by
Bamforth, F J
Johnson, J L
Davidson, A G
Wong, L T
Lockitch, G
Applegarth, D A
Producer:
19910329
In:
Clinical biochemistry
vol. 23
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117.
The high incidence of valproate hepatotoxicity in infants may relate to familial metabolic defects.
[electronic resource]
by
Appleton, R E
Farrell, K
Applegarth, D A
Dimmick, J E
Wong, L T
Davidson, A G
Producer:
19900731
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 17
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118.
Non-concordance of CVS and liver glycine cleavage enzyme in three families with non-ketotic hyperglycinaemia (NKH) leading to false negative prenatal diagnoses.
[electronic resource]
by
Applegarth, D A
Toone, J R
Rolland, M O
Black, S H
Yim, D K
Bemis, G
Producer:
20000630
In:
Prenatal diagnosis
vol. 20
Online resources:
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119.
Free and total serum valproate concentrations: their relationship to seizure control, liver enzymes and plasma ammonia in children.
[electronic resource]
by
Farrell, K
Abbott, F S
Orr, J M
Applegarth, D A
Jan, J E
Wong, P K
Producer:
19861016
In:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
vol. 13
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120.
Prenatal diagnosis of pyruvate carboxylase deficiency.
[electronic resource]
by
Robinson, B H
Toone, J R
Benedict, R P
Dimmick, J E
Oei, J
Applegarth, D A
Producer:
19850326
In:
Prenatal diagnosis
vol. 5
Online resources:
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