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New York State Journal of Medicine
|
January 15, 1971
Hazards in routine use of peritoneal dialysis
R Matalon, S Levine, R P Eisinger
Journal of the American Dental Association (1939)
|
December 1, 1983
Delayed dental age in hepatorenal glycogen storage disease
H T Loevy, R Matalon, I M Rosenthal
Ophthalmology
|
February 1, 1986
Galactokinase activity in patients with idiopathic cataracts
M J Elman, M T Miller, R Matalon
Journal of Inherited Metabolic Disease
|
January 1, 1988
Carrier detection for Sanfilippo A syndrome
R Matalon, M Deanching, R Marback, et al.
Advances in Pediatrics
|
January 1, 1989
Hyperphenylalaninemia due to inherited deficiencies of tetrahydrobiopterin
R Matalon, K Michals, N Blau, et al.
Biomedical & Environmental Mass Spectrometry
|
October 1, 1988
Analysis of the pentafluorobenzoyl derivative of phenylethylamine utilizing negative ion chemical ionization and gas chromatography/mass spectrometry
P Gashkoff, R Matalon, V Papa, et al.
The Journal of Pediatrics
|
February 1, 1981
Linguistic development of children with phenylketonuria and normal intelligence
C R Melnick, K K Michals, R Matalon
Journal of Inherited Metabolic Disease
|
January 1, 1992
Prenatal diagnosis of Canavan disease
R Matalon, K Michals, P Gashkoff, et al.
Journal of the American College of Nutrition
|
April 1, 1997
Phenylketonuria: current dietary treatment practices in the United States and Canada
R O Fisch, R Matalon, S Weisberg, et al.
American Journal of Medical Genetics
|
August 1, 1990
Transmission of ring 14 chromosome from mother to two sons
R Matalon, P Supple, H Wyandt, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 185) with videos related to
Sort By:
Page
of 19
New York State Journal of Medicine
|
January 15, 1971
Hazards in routine use of peritoneal dialysis
R Matalon, S Levine, R P Eisinger
Journal of the American Dental Association (1939)
|
December 1, 1983
Delayed dental age in hepatorenal glycogen storage disease
H T Loevy, R Matalon, I M Rosenthal
Ophthalmology
|
February 1, 1986
Galactokinase activity in patients with idiopathic cataracts
M J Elman, M T Miller, R Matalon
Journal of Inherited Metabolic Disease
|
January 1, 1988
Carrier detection for Sanfilippo A syndrome
R Matalon, M Deanching, R Marback, et al.
Advances in Pediatrics
|
January 1, 1989
Hyperphenylalaninemia due to inherited deficiencies of tetrahydrobiopterin
R Matalon, K Michals, N Blau, et al.
Biomedical & Environmental Mass Spectrometry
|
October 1, 1988
Analysis of the pentafluorobenzoyl derivative of phenylethylamine utilizing negative ion chemical ionization and gas chromatography/mass spectrometry
P Gashkoff, R Matalon, V Papa, et al.
The Journal of Pediatrics
|
February 1, 1981
Linguistic development of children with phenylketonuria and normal intelligence
C R Melnick, K K Michals, R Matalon
Journal of Inherited Metabolic Disease
|
January 1, 1992
Prenatal diagnosis of Canavan disease
R Matalon, K Michals, P Gashkoff, et al.
Journal of the American College of Nutrition
|
April 1, 1997
Phenylketonuria: current dietary treatment practices in the United States and Canada
R O Fisch, R Matalon, S Weisberg, et al.
American Journal of Medical Genetics
|
August 1, 1990
Transmission of ring 14 chromosome from mother to two sons
R Matalon, P Supple, H Wyandt, et al.
Page
of 19