Publications by Hsia D | LitMetric

Publications by authors named "Hsia D"

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MECHANISMS FOR THE DECREASE OF BRAIN SEROTONIN.

D Y HSIA K NISHIMURA Y BRENCHLEY

Nature

November 1963

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INHIBITION OF GLUCURONOSYL TRANSFERASE BY STEROID HORMONES.

D Y HSIA S RIABOV R M DOWBEN

Arch Biochem Biophys

November 1963

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

W F ROWLEY O TANNRIKULU A GROSSMAN D Y HSIA

J Pediatr

June 1963

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Glucose-6-phosphate dehydrogenase deficiency in Taiwan.

T C LEE L Y SHIH P C HUANG C C LIN B N BLACKWELL

Am J Hum Genet

June 1963

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

S JAKOVCIC D Y HSIA

J Pediatr

January 1963

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Serum phenylalanine and tyrosine levels in the newborn infant.

D Y HSIA M LITWACK M O'FLYNN S JAKOVCIC

N Engl J Med

November 1962

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Diet in relation to hereditary metabolic disorders.

D Y HSIA M O'FLYNN

Pediatr Clin North Am

November 1962

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Variability in the clinical manifestations of galactosemia.

D Y HSIA F A WALKER

J Pediatr

August 1962

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Galactosemia: a study of twenty-seven kindreds in North America.

F A WALKER D Y HSIA H M SLATIS A G STEINBERG

Ann Hum Genet

May 1962

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Lipoprotein lipase in cystic fibrosis of the pancreas.

J SLACK S NAIR H TRAISMAN G BECKER S MAHLER

J Lab Clin Med

February 1962

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Clinical management of phenylketonuria.

D Y HSIA W ROWLEY N J RASKIN

Q Bull Northwest Univ Med Sch

November 1998

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[Human biochemical genetics].

Duodecim

November 1998

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Galactosemia: clinical, genetic, and biochemical study.

D Y HSIA T INOUYE F A WALKER

JAMA

December 1961

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Variability in the clinical manifestations of galactosemia.

D Y HSIA F A WALKER

J Pediatr

December 1961

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Blood glucose-6-phosphate in heterozygous carriers and patients with liver glycogen disease (Von Gierke's disease).

J E SOKAL S FLEISSNER E J SARCIONE C U LOWE D Y HSIA

Nature

October 1961

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Epinephrine metabolism in phenylketonuria.

H L NADLER D Y HSIA

Proc Soc Exp Biol Med

November 1998

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A manometric assay for glucose-6-phosphate dehydrogenase.

J A SCHNEIDER M TANNENBAUM D Y HSIA

Clin Chim Acta

July 1961

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Inborn errors of carbohydrate metabolism.

Diabetes

November 1998

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Genetic errors of metabolism and environmental interaction: a synthesis.

Ann N Y Acad Sci

June 1961

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

D Y HSIA W A ROWLEY I HUANG

J Ment Defic Res

June 1961

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The metabolism of indole-compounds in phenvlketonuria.

D Y HSIA I HUANG

Cereb Palsy Bull

June 1961

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Metabolism of 5-hydroxyindole compounds in experimentally produced phenylketonuric rats.

I HUANG S TANNENBAUM L BLUME D Y HSIA

Proc Soc Exp Biol Med

March 1961

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

K HUGH-JONES J SLACK K SIMPSON A GROSSMAN D Y HSIA

N Engl J Med

December 1960

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The genetic mechanism of galactosaemia.

K HUGH-JONES A L NEWCOMB D Y HSIA

Arch Dis Child

December 1960

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Recent developments in inborn errors of metabolism.

Am J Public Health Nations Health

November 1960

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