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Results of search for 'au:"STANLEY, C A"', page 4 of 6
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Authors
Aguilar-Bryan, L
Anday, E K
Baker, L
Bennett, M J
Berry, G T
Bonnefont, J P
Coates, P M
Corkey, B E
Douglas, S D
Ferry, R J
Glaser, B
Hale, D E
Hsu, B Y
Kelly, A
Kilpatrick, L
Nestorowicz, A
Permutt, M A
Stanley, C A
Thornton, P S
Treem, W R
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Adolescent
Adult
Carnitine
Child
Child, Preschool
Fasting
Fatty Acids
Female
Humans
Hyperinsulinism
Hypoglycemia
Infant
Infant, Newborn
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blood
deficiency
diagnosis
etiology
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61.
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1b.
[electronic resource]
by
Korchak, H M
Garty, B Z
Stanley, C A
Baker, L
Douglas, S D
Kilpatrick, L
Producer:
19930805
In:
European journal of pediatrics
vol. 152 Suppl 1
Online resources:
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62.
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder.
[electronic resource]
by
Thornton, P S
Sumner, A E
Ruchelli, E D
Spielman, R S
Baker, L
Stanley, C A
Producer:
19911218
In:
The Journal of pediatrics
vol. 119
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63.
Detection and quantitation of acylcarnitines in plasma and blood spots from patients with inborn errors of fatty acid oxidation.
[electronic resource]
by
Schmidt-Sommerfeld, E
Penn, D
Duran, M
Rinaldo, P
Bennett, M J
Santer, R
Stanley, C A
Producer:
19921218
In:
Progress in clinical and biological research
vol. 375
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64.
Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor.
[electronic resource]
by
Katz, L E
Ferry, R J
Stanley, C A
Collett-Solberg, P F
Baker, L
Cohen, P
Producer:
19991006
In:
The Journal of clinical endocrinology and metabolism
vol. 84
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65.
Acarbose treatment of postprandial hypoglycemia in children after Nissen fundoplication.
[electronic resource]
by
Ng, D D
Ferry, R J
Kelly, A
Weinzimer, S A
Stanley, C A
Katz, L E
Producer:
20020125
In:
The Journal of pediatrics
vol. 139
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66.
Dual regulation of insulin-like growth factor binding protein-1 levels by insulin and cortisol during fasting.
[electronic resource]
by
Katz, L E
Satin-Smith, M S
Collett-Solberg, P
Baker, L
Stanley, C A
Cohen, P
Producer:
19990111
In:
The Journal of clinical endocrinology and metabolism
vol. 83
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67.
Fetal and neonatal hazards of maternal hydration with 5% dextrose before caesarean section.
[electronic resource]
by
Kenepp, N B
Kumar, S
Shelley, W C
Stanley, C A
Gabbe, S G
Gutsche, B B
Producer:
19820722
In:
Lancet (London, England)
vol. 1
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68.
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators.
[electronic resource]
by
Stanley, C A
Fang, J
Kutyna, K
Hsu, B Y
Ming, J E
Glaser, B
Poncz, M
Producer:
20000706
In:
Diabetes
vol. 49
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69.
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome.
[electronic resource]
by
Hsu, B Y
Kelly, A
Thornton, P S
Greenberg, C R
Dilling, L A
Stanley, C A
Producer:
20010405
In:
The Journal of pediatrics
vol. 138
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70.
Cerebral metabolic response and mitochondrial activity following insulin-induced hypoglycemia in newborn lambs.
[electronic resource]
by
Belik, J
Wagerle, L C
Stanley, C A
Sacks, L M
Herbert, D W
Delivoria-Papadopoulos, M
Producer:
19890710
In:
Biology of the neonate
vol. 55
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71.
Impaired chemotaxis and neutrophil (polymorphonuclear leukocyte) function in glycogenosis type IB.
[electronic resource]
by
Koven, N L
Clark, M M
Cody, C S
Stanley, C A
Baker, L
Douglas, S D
Producer:
19860627
In:
Pediatric research
vol. 20
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72.
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.
[electronic resource]
by
Glaser, B
Furth, J
Stanley, C A
Baker, L
Thornton, P S
Landau, H
Permutt, M A
Producer:
19990921
In:
Human mutation
vol. 14
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73.
Genetics of type II diabetes.
[electronic resource]
by
Permutt, M A
Chiu, K
Ferrer, J
Glaser, B
Inoue, H
Nestorowicz, A
Stanley, C A
Tanizawa, Y
Producer:
19981106
In:
Recent progress in hormone research
vol. 53
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74.
The personal experience of juvenile Huntington's disease: an interpretative phenomenological analysis of parents' accounts of the primary features of a rare genetic condition.
[electronic resource]
by
Smith, J A
Brewer, H M
Eatough, V
Stanley, C A
Glendinning, N W
Quarrell, O W J
Producer:
20071018
In:
Clinical genetics
vol. 69
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75.
Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome.
[electronic resource]
by
Kelly, A
Ng, D
Ferry, R J
Grimberg, A
Koo-McCoy, S
Thornton, P S
Stanley, C A
Producer:
20010906
In:
The Journal of clinical endocrinology and metabolism
vol. 86
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76.
Renal handling of carnitine in secondary carnitine deficiency disorders.
[electronic resource]
by
Stanley, C A
Berry, G T
Bennett, M J
Willi, S M
Treem, W R
Hale, D E
Producer:
19930922
In:
Pediatric research
vol. 34
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77.
Hyperfiltration and renal disease in glycogen storage disease, type I.
[electronic resource]
by
Baker, L
Dahlem, S
Goldfarb, S
Kern, E F
Stanley, C A
Egler, J
Olshan, J S
Heyman, S
Producer:
19891006
In:
Kidney international
vol. 35
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78.
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
[electronic resource]
by
Glaser, B
Ryan, F
Donath, M
Landau, H
Stanley, C A
Baker, L
Barton, D E
Thornton, P S
Producer:
19990811
In:
Diabetes
vol. 48
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79.
Interferon-gamma corrects the respiratory burst defect in vitro in monocyte-derived macrophages from glycogen storage disease type 1b patients.
[electronic resource]
by
McCawley, L J
Korchak, H M
Cutilli, J R
Stanley, C A
Baker, L
Douglas, S D
Kilpatrick, L
Producer:
19940418
In:
Pediatric research
vol. 34
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80.
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome.
[electronic resource]
by
Corkey, B E
Hale, D E
Glennon, M C
Kelley, R I
Coates, P M
Kilpatrick, L
Stanley, C A
Producer:
19881026
In:
The Journal of clinical investigation
vol. 82
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