D. Hsia

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Clinical variants of galactosemia.

D. Hsia, 1967, Metabolism: clinical and experimental.

A case of classical maple syrup urine disease “Thiamine non‐responsive”

P. Wong, D. Hsia, P. Justice, 1972, Clinical genetics.

Phenylalanine-hydroxylase activity in hyperphenylalaninaemia.

D. Hsia, P. Justice, M. O'Flynn, 1967, Lancet.

Prolonged obstructive jaundice in infancy.

L. Diamond, D. Hsia, F. Allen, 1952, A.M.A. American journal of diseases of children.

Prolonged obstructive jaundice in infancy. V. The genetic components in neonatal hepatitis.

S. Driscoll, D. Hsia, S. Gellis, 1958, A.M.A. journal of diseases of children.

Down's syndrome. A critical review of the biochemical and immunological data.

R. Dowben, D. Hsia, P. Justice, 1971, American journal of diseases of children.

Identification of Galactose-6-Phosphate in Galactosæmic Erythrocytes

M. Tannenbaum, T. Inouye, D. Hsia, 1962, Nature.

Detection of Heterozygous Carriers in Glycogen Storage Disease of the Liver (von Gierke's Disease)

D. Hsia, E. Kot, E. Kot, 1959, Nature.

Study of hereditary metabolic diseases using in vitro techniques.

D. Hsia, 1970, Metabolism: clinical and experimental.

Use of white blood cells and cultured somatic cells in clinical genetic disorders

D. Hsia, 1970 .

Human Developmental Genetics

D. Hsia, 1968 .

The Infant of the Diabetic Mother

D. Hsia, S. Gellis, 1959 .

A case of phenylketonuria with borderline intelligence.

R. Paine, D. Hsia, W. Knox, 1957, A.M.A. journal of diseases of children.

The laboratory detection of heterozygotes.

D. Hsia, 1957, American journal of human genetics.

Galactosemia: A study of twenty‐seven kindreds in North America *

A. Steinberg, H. Slatis, D. Hsia, 1962, Annals of human genetics.

Utilization of leukocytes for the study of inborn errors of metabolism.

D. Hsia, 1972, Enzyme.

Development of 5-Hydroxytryptophan Decarboxylase Activity in Rat Kidney

D. Hsia, S. Tannenbaum, I. Huang, 1960, Nature.

Amylo-1, 6-glucosidase in human fibroblasts: Studies in Type III glycogen storage disease

D. Hsia, P. Justice, C. Ryan, 1970 .

BIOCHEMICAL CHANGES IN CHROMOSOMAL ABNORMALITIES *

L. Shih, D. Hsia, H. Nadler, 1969 .

INHIBITION OF GLUCURONOSYL TRANSFERASE BY STEROID HORMONES.

R. Dowben, D. Hsia, S. Riabov, 1963, Archives of biochemistry and biophysics.

The Genetic Mechanism of Gaucher's Disease1,2

J. Naylor, D. Hsia, J. A. Bigler, 1962 .

The detection of heterozygous carriers.

D. Hsia, 1969, The Medical clinics of North America.

The dietary phenylalanine requirements and tolerances of phenylketonuric patients.

R. Paine, D. Hsia, 1957, A.M.A. journal of diseases of children.

Altered sex ratio among phenylketonuric infants ascertained by screening the newborn.

D. Hsia, J. Dobson, 1970, Lancet.

Atypical phenylketonuria with borderline or normal intelligence.

D. Hsia, M. O'Flynn, J. Berman, 1968, American journal of diseases of children.

Utilization of white blood cells for study of clinical genetic disorders

D. Hsia, H. Nadler, 1967 .

INHIBITORS OF GLUCURONYL TRANSFERASE IN THE NEWBORN *

R. Dowben, D. Hsia, Svetislav Riabov, 1963, Annals of the New York Academy of Sciences.

Hyperphenylalanemia without phenylketonuria.

P. Tillman, D. Hsia, M. O'Flynn, 1967, American journal of diseases of children.

Glutamine in pku.

M. Partington, P. Wong, D. Hsia, 1971, The New England journal of medicine.

EFFECT OF VITAMIN B6ON BLOOD 5-HYDROXYTRYPTAMINE CONCENTRATION

D. Hsia, P. Justice, J. Berman, 1969 .

Causes for high phenylalanine with normal tyrosine in newborn screening programs.

G. Cunningham, D. Hsia, J. Berman, 1969, American journal of diseases of children.

Metabolic disorders associated with mental retardation.

D. Hsia, P. Justice, H. Nadler, 1968, Pediatric clinics of North America.

SCREENING NEWBORN INFANTS FOR PHENYLKETONURIA.

H. Slatis, D. Hsia, J. Berman, 1964, JAMA.

Serum phenylalanine and tyrosine levels in the newborn infant.

S. Jakovcic, D. Hsia, M. Litwack, 1962, New England Journal of Medicine.

Diet in relation to hereditary metabolic disorders.

D. Hsia, M. O'Flynn, 1962, Pediatric clinics of North America.

Detection by Phenylalanine Tolerance Tests of Heterozygous Carriers of Phenylketonuria

D. Hsia, W. Troll, W. Knox, 1956, Nature.

CEREBROSIDE METABOLISM IN EXPERIMENTAL PHENYLKETONURIA AND GALACTOSEMIA

T. Inouye, D. Hsia, P. Justice, 1967 .

PARTIAL PURIFICATION OF HEXOSE-1-PHOSPHATE URIDYLTRANSFERASE FROM HUMAN RED CELLS.

T. Inouye, D. Hsia, S. Riabov, 1965, Biochimica et biophysica acta.

STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME.

P. Wong, T. Inouye, D. Hsia, 1964, The New England journal of medicine.

Variability in the clinical manifestations of galactosemia.

D. Hsia, F. A. Walker, David Yi-Yung Hsia, 1961, The Journal of pediatrics.

Inborn errors of carbohydrate metabolism.

D. Hsia, 1961, Diabetes.

GENETIC ERRORS OF METABOLISM AND ENVIRONMENTAL INTERACTION: A SYNTHESIS *

D. Hsia, 1961, Annals of the New York Academy of Sciences.

The Genetic Mechanism of Galactosaemia*

A. L. Newcomb, D. Hsia, K. Hugh-Jones, 1960, Archives of disease in childhood.

Hereditary Metabolic Disorders Involving the Nervous System

D. Hsia, J. Slack, K. Simpson, 1960 .

Serum Bilirubin Levels and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborn American Negroes.

D. Hsia, M. O'Flynn, 1963 .

BIRTH WEIGHT IN CYSTIC FIBROSIS OF THE PANCREAS *

D. Hsia, 1959, Annals of human genetics.

Prolonged obstructive jaundice in infancy. IV. Neonatal hepatitis.

J. Craig, D. Hsia, S. Gellis, 1954, A.M.A. American journal of diseases of children.

Family outbreaks of infectious hepatitis; prophylactic use of gamma globulin.

D. Hsia, S. Gellis, B. Brooks, 1953, The New England journal of medicine.

Inhibition of Glucuronosyl Transferase by Progestational Agents from Serum of Pregnant Women

R. Dowben, D. Hsia, A. Grossman, 1960, Nature.

THE DIAGNOSIS OF CARRIERS OF DISEASE‐PRODUCING GENES *

D. Hsia, 1966 .

Summary of a symposium on phototherapy for hyperbilirubinemia.

R. Behrman, D. Hsia, 1969, Birth defects original article series.

REACTION OF ALKALI METAL CYANIDES WITH ALKYL HALIDES IN HMPA OR HMPA CONTAINING CROWN ETHER

T. Sawyer, G. Parries, D. Hsia, 1978 .

Epinephrine Metabolism in Phenylketonuria.∗

D. Hsia, H. Nadler, 1961, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

The Metabolism of Indole‐Compounds in Phenylketonuria

D. Hsia, I. Huang, 1961, Cerebral palsy bulletin.

Pathogenetic problems in phenylketonuria.

D. Hsia, W. Knox, 1957, The American journal of medicine.

Studies on respiratory rate in the newborn; its use in the evaluation of respiratory distress in infants of diabetic mothers.

D. Hsia, S. Gellis, H. Haddad, 1956, Pediatrics.

The nature of disaccharidases in human leukocytes.

D. Hsia, J. Farquhar, J. Monteleleone, 1969, The Journal of laboratory and clinical medicine.

Genetic and Biochemical Aspects of Reproductive Failure

D. Hsia, 1967 .

Studies on the relation between serum and spinal fluid bilirubin during early infancy.

D. Hsia, M. Nasralla, E. Gawronska, 1958, The Journal of clinical investigation.

Clinical course of hyperbilirubinemia in premature infants. A preliminary report.

D. Hsia, J. Slack, K. Simpson, 1960, The New England journal of medicine.

Enzyme changes and polyribosome profiles in phytohemagglutinin stimulated lymphocytes.

R. Dowben, D. Hsia, H. Nadler, 1969, Blood.

Gamma globulin in the prevention of infectious hepatitis; studies on the use of small doses in family outbreaks.

D. Hsia, S. Gellis, M. Lonsway, 1954, The New England journal of medicine.

Enzymes in trisomy-18 syndrome.

T. Inouye, D. Hsia, H. Nadler, 1966, Lancet.

Serum-alkaline-phosphatase in cystic fibrosis of the pancreas.

L. Shih, D. Hsia, P. Justice, 1969, Lancet.

BIOCHEMICAL CHANGES IN CHROMOSOMAL ABNORMALITIES *

L. Shih, D. Hsia, H. Nadler, 1968 .

ISOENZYMES IN DOWN'S SYNDROME

D. Hsia, H. Nadler, P. Monteleone, 1967 .

Polyribosomes from L cells.

R. Dowben, D. Hsia, H. Nadler, 1969, Experimental cell research.

Lymphocyte and granulocyte enzyme activity in patients with Down's syndrome.

T. Inouye, D. Hsia, H. Nadler, 1967, Blood.

Cirrhosis of the liver in infants and children.

J. Craig, D. Hsia, S. Gellis, 1955, A.M.A. American journal of diseases of children.

Jaundice in infancy.

D. Hsia, S. Gellis, 1955, Pediatric clinics of North America.

BIRTH WEIGHT IN INFANTS OF DIABETIC MOTHERS

D. Hsia, S. Gellis, 1957, Annals of human genetics.

ENZYMES IN DOWN'S SYNDROME

P. Wong, T. Inouye, L. Shih, 1965 .

Enzymes in Cultivated Human Fibroblasts derived from Patients with Down's Syndrome (Mongolism)

T. Inouye, D. Hsia, P. Justice, 1967, Nature.

Enzymes in cultivated human fibroblasts derived from patients with autosomal trisomy syndromes.

T. Inouye, D. Hsia, H. Nadler, 1967, American journal of human genetics.

β-Galactosidase activity in human intestinal lactases

G. Semenza, A. Prader, M. Makler, 1966 .

Portal hypertension in infants and children.

D. Hsia, S. Gellis, 1955, A.M.A. American journal of diseases of children.

Studies on Inhibition of Brain 5-Hydroxytryptophan Decarboxylase by Phenylalanine Metabolites.∗

D. Hsia, P. Justice, 1965, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

Studies on Inhibition of 5-Hydroxy Tryptophan Decarboxylase by Phenylalanine Metabolites.∗

D. Hsia, I. Huang, 1963, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

THE INFLUENCE OF SERUM BILIRUBIN LEVELS UPON THE ULTIMATE DEVELOPMENT OF LOW BIRTHWEIGHT INFANTS.

J. Cosbey, D. Hsia, N. Haimowitz, 2008, Journal of mental deficiency research.

Serum bilirubin levels in the newborn infant.

L. Diamond, D. Hsia, F. Allen, 1953, The Journal of pediatrics.

A long-term follow-up study on infectious hepatitisduring pregnancy

D. Hsia, S. Gellis, Robert G. Taylor, 1952 .

Activity of glucose-6-phosphate dehydrogenase in erythrocyes of patients with various abnormal hemoglobins.

J. Naylor, D. Hsia, I. Schulman, 1960, Pediatrics.

STUDIES ON THE EFFECT OF NOVOBIOCIN ON GLUCURONYL TRANSFERASE

R. Dowben, D. Hsia, H. Lokietz, 1963 .

A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria.

R. Paine, D. Hsia, W. Knox, 1958, Pediatrics.

A controlled study on effect of promethazine hydrochloride and meperidine hydrochloride upon serum bilirubin levels in the newborn infant

D. Hsia, A. Grossman, W. Rowley, 1963 .

The Role of Phenylalanine in Mental Development

D. Hsia, 1969 .

Some observations on the dietary treatment of phenylketonuria.

D. Hsia, M. O'Flynn, 1968, The Journal of pediatrics.

Clinical management of phenylketonuria.

N. Raskin, D. Hsia, W. Rowley, 1962, Quarterly bulletin. Northwestern University (Evanston, Ill.). Medical School.

Recent developments in inborn errors of metabolism.

D. Hsia, 1960, American journal of public health and the nation's health.

Studies on linkage between phenylketonuria and the blood groups.

A. Steinberg, D Y HSIA, A G STEINBERG, 1960, American journal of human genetics.

Phenylketonuria: the phenylalanine-tyrosine ratio in the detection of the heterozygous carrier.

D Y Y HSIA, D. Hsia, D. Y. Hsia, 1958, Journal of mental deficiency research.

NUTRITIONAL MANAGEMENT IN HEREDITARY METABOLIC DISEASE

D. Hsia, 1968, Developmental medicine and child neurology.

The metabolism of 5-hydroxytryptamine (serotonin) in the newborn.

D. Hsia, P. Justice, J. Berman, 1965, The Journal of pediatrics.

Screening for galactosemia and glucose-6-phosphate dehydrogenase deficiency in newborn infants.

D. Hsia, K. Nelson, 1967, Jornal de Pediatria.

Further studies on the heterozygous carrier in galactosemia.

M. Tannenbaum, D. Hsia, K. Simpson, 1960, The Journal of laboratory and clinical medicine.

Enzymatic Oxidation of Galactose-6-phosphate

T. Inouye, D. Hsia, J. A. Schneider, 1964, Nature.

Variability in the clinical manifestations of galactosemia.

D. Hsia, F. A. Walker, 1962, The Journal of pediatrics.

Lipoprotein lipase in cystic fibrosis of the pancreas.

D. Hsia, H. Traisman, S. Nair, 1962, The Journal of laboratory and clinical medicine.

Studies on the genetic mechanism of cystic fibrosis of the pancreas.

D. Hsia, M. Smoller, 1959, A.M.A. journal of diseases of children.

Abnormal sweat electrolytes in patients with allergies; a preliminary report.

S. Driscoll, D. Hsia, T. C. Lee, 1958, A.M.A. journal of diseases of children.

Studies on mechanism for decreased lipoprotein lipase in cystic fibrosis of the pancrease.

S. Jakovcic, D. Hsia, 1963, The Journal of pediatrics.

Pregnancy in the diabetic mother with nephritis.

D. Hsia, T. Oppé, S. Gellis, 1957, Lancet.

Studies on erythroblastosis due to ABO incompatibility.

D. Hsia, S. Gellis, 1953, Pediatrics.

Brain Serotonin in Experimental Tyrosinosis

D. Hsia, P. Justice, J. Berman, 1964, Nature.

Mechanisms for the Decrease of Brain Serotonin

K. Nishimura, D. Hsia, Yvonne Brenchley, 1963, Nature.

HOMOLOGOUS SERUM‐HEPATITIS FOLLOWING THE USE OF FRACTION IV PREPARED FROM POSTPARTUM PLASMA: A report of four cases

J. Kennell, D. Hsia, S. Gellis, 1953, The American journal of the medical sciences.

The development of enzyme systems during early infancy.

S. Driscoll, D. Hsia, 1958, Pediatrics.

Characterization of leukocyte glucose-6-phosphate dehydrogenase in normal and mutant human subjects.

L. Shih, D. Hsia, P. Justice, 1966, The Journal of laboratory and clinical medicine.

Electrophoretic mobility of glucose-6-phosphate dehydrogenase in lymphocytes and granulocytes.

D. Hsia, P. Justice, H. Nadler, 1967, Clinica chimica acta; international journal of clinical chemistry.

Congenital nonspherocytic hemolytic anemia associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a Negro family.

D. Hsia, P. Justice, N. Shahidi, 1966, Pediatrics.

Glucose-6-phosphate dehydrogenase deficiency in Taiwan.

L. Shih, D. Hsia, R. Blackwell, 1963, American journal of human genetics.

The genetic mechanism of idiopathic hyperlipemia.

D. Hsia, J. Boggs, R. F. Mais, 1957, The New England journal of medicine.

Prolonged obstructive jaundice in infancy. I. General survey of 156 cases.

L. Diamond, D. Hsia, F. Allen, 1952, Pediatrics.

Penylketonuria detection of the heterozygous carrier.

R. Paine, D. Hsia, 2008, Journal of mental deficiency research.

Inborn Errors of Metabolism

D. Hsia, 1959 .

INBORN ERRORS OF METABOLISM, PART 2: LABORATORY METHODS

T. Inouye, D. Hsia, 1966 .

Gaucher's disease; report of two cases in father and son and review of the literature.

J. Naylor, D. Hsia, J. A. Bigler, 1959, The New England journal of medicine.

The distribution of genetic polymorphisms among patients with Down's syndrome, phenylketonuria, and cystic fibrosis of the pancreas.

L. Shih, D. Hsia, J. Farquhar, 1969, American journal of human genetics.

Tissue Cystathionine in Mice Treated With Cysteine and Homoserine

P. Wong, D. Hsia, R. Fresco, 1970, Pediatric Research.

Conference on sex ratio in phenylketonuria.

R. Koch, D. Hsia, L. Woolf, 1971, The Journal of pediatrics.

Sex ratio in phenylketonuria.

R. Koch, D. Hsia, L. Woolf, 1970, The Lancet.

Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.

G. Cunningham, D. Hsia, J. Berman, 1969, American journal of diseases of children.

Detection of the heterozygous carriers of phenylketonuria.

D. Hsia, K. Driscoll, 1956, Lancet.

The nature and origin of X chromosome aberrations in Turner's syndrome

D. Hsia, 1964 .

Phenylketonuria and its variants.

D. Hsia, 1970, Progress in medical genetics.

PHENYLKETONURIA: A STUDY OF HUMAN BIOCHEMICAL GENETICS E. Mead Johnson Award Address, October 26, 1965

D. Hsia, 1966 .

Studies on the mechanical fragility of erythrocytes. I. Normal values for infants and children.

R. Goldbloom, D. Hsia, J. Reinhold, 1953, Blood.

Liver function tests in infants and children.

D. Hsia, S. Gellis, 1955, Pediatric clinics of North America.

Prolonged obstructive jaundice in infancy. III. Liver function tests.

D. Hsia, S. Gellis, 1953, A.M.A. American journal of diseases of children.

Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus.

L. Diamond, D. Hsia, F. Allen, 1952, The New England journal of medicine.

Enzyme studies during lymphocyte stimulation with phytohemagglutinin in Down's syndrome.

D. Hsia, H. Nadler, P. Monteleone, 1967, Life sciences.

Genetic studies on vitamin D resistant rickets (familial hypophosphatemia).

D. Hsia, M. Kraus, J. Samuels, 1959, American journal of human genetics.

The development of intestinal -galactosidase and -glucuronidase in the newborn

D. Hsia, 1966 .

Beta-galactosidase activity in human intestinal lactases.

A. Prader, M. Makler, D. Hsia, 1966, Biochimica et Biophysica Acta.

"Neonatal Hepatitis" in Twin Pregnancy

P. Wong, D. Hsia, R. Burnstine, 1965, Pediatrics.

Studies on the relation of mechanical fragility of erythrocytes to physiological jaundice.

R. Goldbloom, D. Hsia, S. Gellis, 1953, A.M.A. American journal of diseases of children.

The Heterozygous Carrier in Galactosæmia

S. Driscoll, D. Hsia, I. Huang, 1958, Nature.

Recent developments in the study of hereditary diseases in children.

D. Hsia, 1957, Postgraduate medicine.

The excretion of 5-hydroxyindoleacetic acid in the heterozygous carrier for phenylketonuria.

W. Rowley, D. Hsia, I. Huang, 1961, Journal of mental deficiency research.

Metabolism of 5-Hydroxyindole Compounds in Experimentally Produced Phenylketonuric Rats.∗ †

D. Hsia, S. Tannenbaum, I. Huang, 1961, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

THIN-LAYER CHROMATOGRAPHIC ANALYSIS OF PLASMA PHOSPHOLIPIDS IN ESSENTIAL FAMILIAL HYPERLIPIDEMIA.

S. Jakovcic, D. Hsia, J. C. Christian, 1964, The Journal of laboratory and clinical medicine.

Hepatic dysfunction in infectious mononucleosis in children.

D. Hsia, S. Gellis, 1952, A.M.A. American journal of diseases of children.

The mechanism of blue light on neonatal jaundice.

D. Hsia, S. Porto, 1969, The Journal of pediatrics.

The hyperlipidemia in glycogen storage disease.

A. Khachadurian, S. Jakovcic, D. Hsia, 1966, The Journal of laboratory and clinical medicine.

Amylo-1,6-glucosidase in human fibroblasts: studies 3 glycogen storage disease.

D. Hsia, P. Justice, C. Ryan, 1970, Biochemical and biophysical research communications.

LEUCOCYTE TRANSFERASE IN NEGROES

T. Inouye, D. Hsia, H. Nadler, 1967 .

Triple X female and a Down's syndrome offspring.

D. Hsia, G. F. Smith, J. Singer, 1972, Journal of medical genetics.

Neonatal jaundice.

D. Hsia, S. Porto, David Evans, 2007, BMJ clinical evidence.

Experimental studies on blood-spinal fluid barrier for bilirubin.

D. Hsia, T. C. Lee, 1959, The Journal of laboratory and clinical medicine.

A micromethod for serum bilirubin.

H. Hsia, D. Hsia, S. Gellis, 1952, The Journal of laboratory and clinical medicine.

Determination of concentration of bilirubin in serum. I. Rapid micro-method employing photoelectric colorimeter. II. Rapid micro-method employing color standards.

H. Hsia, D. Hsia, S. Gellis, 1956, Pediatrics.

Cystic fibrosis of the pancreas.

D. Hsia, M. O'Flynn, W. Rowley, 1966, Advances in cardiopulmonary diseases.

Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus.

L. Diamond, D. Hsia, F. Allen, 1952, The New England journal of medicine.

Inheritance of factor XIII.

L. Lorand, D. Hsia, 1970, American journal of human genetics.

Purification and characterization of genetic variants of 6-phosphogluconate dehydrogenase

L. Shih, D. Hsia, P. Justice, 1968, Biochemical Genetics.

Screening newborn infantsfor galactosemia

D. Hsia, R. Gatti, P. Manfield, 1966 .

Polysomes of Cultured Normal and Leukaemic Lymphocytes: Response to Phytohaemagglutinin

D. Hsia, P. Justice, Y. Rabinowitz, 1973, British journal of haematology.

Inheritance of deficiency of fibrin-stabilizing factor (factor 13).

L. Lorand, D. Hsia, A. Atencio, 1970, American journal of human genetics.

Characterization of Glucose-6-phosphate Dehydrogenase among Chinese

P. Wong, L. Shih, D. Hsia, 1965, Nature.

A manometric assay for glucose-6-phosphate dehydrogenase.

M. Tannenbaum, D. Hsia, J. A. Schneider, 1961, Clinica chimica acta; international journal of clinical chemistry.