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Results of search for 'au:"Hsia, D Y"', page 3 of 9
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Authors
ALLEN, F H
BIGLER, J A
Berman, J L
DIAMOND, L K
DOWBEN, R M
DRISCOLL, S G
GELLIS, S S
GROSSMAN, A
HSIA, D Y
HSIA, D Y Y
HUANG, I
Hsia, D Y
INOUYE, T
JAKOVCIC, S
Justice, P
KNOX, W E
Nadler, H L
O'Flynn, M E
Shih, L Y
Smith, G F
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Topics
Acid Phosphatase
Bilirubin
Child
Erythrocytes
Female
Galactosemias
Glucosephosphate Dehydrogenase
Heterozygote
Humans
Infant
Infant, Newborn
Leukocytes
Male
Phenylalanine
Phenylketonurias
analysis
blood
diagnosis
enzymology
metabolism
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English
Finnish
Your search returned 165 results.
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41.
Detection of the heterozygous carriers of phenylketonuria.
[electronic resource]
by
DRISCOLL, K W
HSIA, D Y
Producer:
20020501
In:
Lancet (London, England)
vol. 271
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42.
Epinephrine metabolism in phenylketonuria.
[electronic resource]
by
NADLER, H L
HSIA, D Y
Producer:
19981101
In:
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.)
vol. 107
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43.
Experimental studies on blood-spinal fluid barrier for bilirubin.
[electronic resource]
by
LEE, T C
HSIA, D Y
Producer:
19981101
In:
The Journal of laboratory and clinical medicine
vol. 54
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44.
Birth weight in infants of diabetic mothers.
[electronic resource]
by
HSIA, D Y
GELLIS, S S
Producer:
20000701
In:
Annals of human genetics
vol. 22
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45.
Detection of heterozygous carriers in glycogen storage disease of the liver (von Gierke's disease).
[electronic resource]
by
HSIA, D Y
KOT, E G
Producer:
20000701
In:
Nature
vol. 183
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46.
The dietary phenylalanine requirements and tolerances of phenylketonuric patients.
[electronic resource]
by
PAINE, R S
HSIA, D Y
Producer:
20000701
In:
A.M.A. journal of diseases of children
vol. 94
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47.
Hyperphenylalanemia.
[electronic resource]
by
Hsia, D Y
O'Flynn, M E
Producer:
19670415
In:
Metabolism: clinical and experimental
vol. 16
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48.
Variability in the clinical manifestations of galactosemia.
[electronic resource]
by
HSIA, D Y
WALKER, F A
Producer:
19981101
In:
The Journal of pediatrics
vol. 59
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49.
Variability in the clinical manifestations of galactosemia.
[electronic resource]
by
HSIA, D Y
WALKER, F A
Producer:
19981101
In:
The Journal of pediatrics
vol. 61
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50.
Predicted and measured exposures from 41Ar released to the atmosphere by a heavy water research reactor.
[electronic resource]
by
Hsia, D Y
Chen, T K
Producer:
19770512
In:
Health physics
vol. 31
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51.
The distribution of genetic polymorphisms among Chinese in Taiwan.
[electronic resource]
by
Shih, L Y
Hsia, D Y
Producer:
19700205
In:
Human heredity
vol. 19
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52.
Summary of a symposium on phototherapy for hyperbilirubinemia.
[electronic resource]
by
Behrman, R E
Hsia, D Y
Producer:
19720202
In:
Birth defects original article series
vol. 6
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53.
Viral hepatitis.
[electronic resource]
by
GELLIS, S S
HSIA, D Y
Producer:
20030501
In:
The New England journal of medicine
vol. 249
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54.
Pathogenetic problems in phenylketonuria.
[electronic resource]
by
KNOX, W E
HSIA, D Y
Producer:
20020501
In:
The American journal of medicine
vol. 22
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55.
Studies on linkage between phenylketonuria and the blood groups.
[electronic resource]
by
HSIA, D Y
STEINBERG, A G
Producer:
19981101
In:
American journal of human genetics
vol. 12
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56.
Jaundice in infancy.
[electronic resource]
by
GELLIS, S S
HSIA, D Y Y
Producer:
20030501
In:
Pediatric clinics of North America
p. 449-64
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57.
The infant of diabetic mother.
[electronic resource]
by
GELLIS, S S
HSIA, D Y Y
Producer:
20000701
In:
A.M.A. journal of diseases of children
vol. 97
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58.
Penylketonuria detection of the heterozygous carrier.
[electronic resource]
by
HSIA, D Y Y
PAINE, R S
Producer:
20000701
In:
Journal of mental deficiency research
vol. 1
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59.
The development of enzyme systems during early infancy.
[electronic resource]
by
DRISCOLL, S G
HSIA, D Y Y
Producer:
20000701
In:
Pediatrics
vol. 22
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60.
Glycogen storage disease previously reported as familial hyperlipidemia.
[electronic resource]
by
Jakovcic, S
Fuhrmann, W
Hsia, D Y
Producer:
19660212
In:
Pediatrics
vol. 36
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