 |
|
| ARTICLES
|
|---|
|
|
|
Mary L. Efron, (Nov 18, 1926, to Sept 2, 1967)
R. Westall
Am J Dis Child. 1969;117:1-2.
|
|
|
|
Mary L. Efron, (Nov. 18, 1926, to Sept. 2, 1967)
R. D. Adams
Am J Dis Child. 1969;117:2-3.
|
|
|
|
Use of human genetic variation to study membrane transport of amino acids in kidney
C. R. Scriver
Am J Dis Child. 1969;117:4-12.
|
|
|
|
Disorders of intestinal transport of amino acids
S. O. Thier; D. H. Alpers
Am J Dis Child. 1969;117:13-23.
|
|
|
|
Blood and urine amino acid aberrations. Physiologic and pathological changes in patients without inborn errors of amino acid metabolism
R. D. Feigin
Am J Dis Child. 1969;117:24-47.
|
|
|
|
Results of mass screening for hyperaminoacidemias in the newborn infant
C. Clow; C. R. Scriver; E. Davies
Am J Dis Child. 1969;117:48-53.
|
|
|
|
Causes for high phenylalanine with normal tyrosine in newborn screening programs
J. L. Berman; G. C. Cunningham; R. W. Day; R. Ford; D. Y. Hsia
Am J Dis Child. 1969;117:54-65.
|
|
|
|
Mental deficiency and a new aminoaciduria
M. G. Ampola; M. L. Efron; E. M. Bixby; E. Meshorer
Am J Dis Child. 1969;117:66-70.
|
|
|
|
Beta-mercaptolactate-cysteine disulfide in the urine of a mentally retarded patient
J. C. Crawhall; R. Parker; W. Sneddon; E. P. Young
Am J Dis Child. 1969;117:71-82.
|
|
|
|
Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation
V. E. Shih; M. L. Efron; H. W. Moser
Am J Dis Child. 1969;117:83-92.
|
|
|
|
A defect in intestinal amino acid transport in Lowe's syndrome
C. S. Bartsocas; H. L. Levy; J. D. Crawford; S. O. Thier
Am J Dis Child. 1969;117:93-95.
|
|
|
|
Hypermethioninemia with other hyperaminoacidemias. Studies in infants on high-protein diets
H. L. Levy; V. E. Shih; P. M. Madigan; V. Karolkewicz; J. R. Carr; A. Lum; A. A. Richards; J. D. Crawford; R. A. MacCready
Am J Dis Child. 1969;117:96-103.
|
|
|
|
D-methioninuria due to DL-methionine ingestion. An artefact detected by a mass screening program for errors of amino acid metabolism
M. L. Efron; T. C. McPherson; V. E. Shih; C. F. Welsh; R. A. MacCready
Am J Dis Child. 1969;117:104-107.
|
|
|
|
Absence of acid maltase in glycogenesis type 2(Pompe's disease) in tissue culture
J. Dancis; J. Hutzler; J. Lynfield; R. P. Cox
Am J Dis Child. 1969;117:108-111.
|
|
|
|
Byler disease. Fatal familial intrahepatic cholestasis in an Amish kindred
R. J. Clayton; F. L. Iber; B. H. Ruebner; V. A. McKusick
Am J Dis Child. 1969;117:112-124.
|
|
