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Results of search for 'au:"Gordon, B A"', page 1 of 3
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Authors
BEVERIDGE, J M
Benson, A C
Bird, S R
Budreau, C H
Coulter-Mackie, M B
DiCioccio, R A
Feleki, V
Fraser, S F
GORDON, B A
Gatfield, D P
Gatfield, P D
Gilbert, J J
Gordon, B A
Gordon, K E
Hahn, A F
Haust, M D
Hechtman, P
Hinton, G G
Rip, J W
Rupar, C A
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Topics
Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Ammonia
Child
Child, Preschool
Female
Fibroblasts
Glycosaminoglycans
Humans
Infant
Liver
Male
Ornithine
analysis
blood
enzymology
genetics
metabolism
pathology
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English
Your search returned 48 results.
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1.
MANAGEMENT OF RECTAL BLEEDING IN INFANTS.
[electronic resource]
by
GORDON, B A
Producer:
19961201
In:
Clinical proceedings - Children's Hospital of the District of Columbia
vol. 21
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2.
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3.
[electronic resource]
by
Gordon, B A
Feleki, V
Producer:
19720503
In:
Clinical biochemistry
vol. 3
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3.
Leukocyte hydrolases in the Sanfilippo syndrome.
[electronic resource]
by
Gordon, B A
Feleki, V
Producer:
19740405
In:
Clinical biochemistry
vol. 4
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4.
Ultrastructural and biochemical aspects of the Sanfilippo syndrome,--type III genetic mucopolysaccharidosis.
[electronic resource]
by
Haust, M D
Gordon, B A
Producer:
19861118
In:
Connective tissue research
vol. 15
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5.
Ultrastructural changes in the mitochondria in disorders in ornithine metabolism.
[electronic resource]
by
Haust, M D
Gordon, B A
Producer:
19810521
In:
Pediatric research
vol. 14
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6.
Methylmalonic acidemia controlled with oral administration of vitamin B12.
[electronic resource]
by
Gordon, B A
Carson, R A
Producer:
19761029
In:
Canadian Medical Association journal
vol. 115
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7.
Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and 3.
[electronic resource]
by
Gordon, B A
Haust, M D
Producer:
19720601
In:
Clinical biochemistry
vol. 4
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8.
Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
[electronic resource]
by
Haust, M D
Gordon, B A
Producer:
19870626
In:
Birth defects original article series
vol. 23
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9.
A simple spectrophotometric enzyme assay with absolute specificity for arylsulfatase A.
[electronic resource]
by
Rip, J W
Gordon, B A
Producer:
19980604
In:
Clinical biochemistry
vol. 31
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10.
Defective expression of alpha-L-fucosidase by lymphoid cells of a fucosidosis patient.
[electronic resource]
by
DiCioccio, R A
Gordon, B A
Producer:
19910926
In:
Clinical biochemistry
vol. 24
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11.
The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases.
[electronic resource]
by
Gordon, B A
Haust, M D
Producer:
19720503
In:
Clinical biochemistry
vol. 3
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12.
Pyomyositis: characteristics at CT and MR imaging.
[electronic resource]
by
Gordon, B A
Martinez, S
Collins, A J
Producer:
19951101
In:
Radiology
vol. 197
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13.
THE EFFECT OF DIETARY FAT ON BILE ACID METABOLISM IN MAN.
[electronic resource]
by
GORDON, B A
KUKSIS, A
BEVERIDGE, J M
Producer:
19961201
In:
Canadian journal of biochemistry
vol. 42
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14.
Ornithine methyl ester. An unusual metabolite encountered in the urine of patients with a urea cycle disorder characterized by hyperammonemia, hyperornithinemia and homocitrullinuria.
[electronic resource]
by
Gordon, B A
Gatfield, P D
Taller, E
Producer:
19770718
In:
Clinical biochemistry
vol. 10
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15.
Unusual clinical and ultrastructural features in a boy with biochemically typical mannosidosis.
[electronic resource]
by
Gordon, B A
Carson, R
Haust, M D
Producer:
19810513
In:
Acta paediatrica Scandinavica
vol. 69
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16.
Whole-body positron emission tomography: normal variations, pitfalls, and technical considerations.
[electronic resource]
by
Gordon, B A
Flanagan, F L
Dehdashti, F
Producer:
19980102
In:
AJR. American journal of roentgenology
vol. 169
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17.
Separation of bile acid conjugates by ion exchange chromatography.
[electronic resource]
by
GORDON, B A
KUKSIS, A
BEVERIDGE, J M
Producer:
19981101
In:
Canadian journal of biochemistry and physiology
vol. 41
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18.
Prefrontal gray matter volume mediates age effects on memory strategies.
[electronic resource]
by
Kirchhoff, B A
Gordon, B A
Head, D
Producer:
20141104
In:
NeuroImage
vol. 90
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19.
Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria.
[electronic resource]
by
Haust, M D
Gatfield, P D
Gordon, B A
Producer:
19810720
In:
Human pathology
vol. 12
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20.
The hyperornithinemia, hyperammonemia, homocitrullinuria syndrome: an ornithine transport defect remediable with ornithine supplements.
[electronic resource]
by
Gordon, B A
Gatfield, D P
Haust, M D
Producer:
19871027
In:
Clinical and investigative medicine. Medecine clinique et experimentale
vol. 10
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