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Pediatric Research
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July 17, 1998
Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A)
A Fischer, K P Carmichael, J F Munnell, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1991
Intellectual development in 12-year-old children treated for phenylketonuria
C G Azen, R Koch, E G Friedman, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'
W B Hanley, C Azen, R Koch, et al.
Journal of Pediatric Hematology/Oncology
|
April 10, 2022
Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case Report
Rameshwar R Rao, Ben W Dulken, Dena R Matalon, et al.
Pediatric Research
|
August 1, 1989
Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancy
J A Wolff, B Barshop, W L Nyhan, et al.
American Journal of Obstetrics and Gynecology
|
April 1, 1992
Maternal phenylketonuria collaborative study, obstetric aspects and outcome: the first 6 years
L D Platt, R Koch, C Azen, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2023
Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome
Dena R Matalon, Elizabeth J Bhoj, Dong Li, et al.
Molecular Genetics and Metabolism
|
September 26, 2000
Maternal phenylketonuria: an international study
R Koch, W Hanley, H Levy, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994
R Koch, H L Levy, R Matalon, et al.
European Journal of Pediatrics
|
July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemia
H L Levy, S E Waisbren, D Lobbregt, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 185) with videos related to
Sort By:
Page
of 19
Pediatric Research
|
July 17, 1998
Sulfamidase deficiency in a family of Dachshunds: a canine model of mucopolysaccharidosis IIIA (Sanfilippo A)
A Fischer, K P Carmichael, J F Munnell, et al.
American Journal of Diseases of Children (1960)
|
January 1, 1991
Intellectual development in 12-year-old children treated for phenylketonuria
C G Azen, R Koch, E G Friedman, et al.
Journal of Inherited Metabolic Disease
|
October 27, 2004
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'
W B Hanley, C Azen, R Koch, et al.
Journal of Pediatric Hematology/Oncology
|
April 10, 2022
Leiomyomatosis in an Infant With a SUFU Splice Site Variant: Case Report
Rameshwar R Rao, Ben W Dulken, Dena R Matalon, et al.
Pediatric Research
|
August 1, 1989
Effects of ascorbic acid in alkaptonuria: alterations in benzoquinone acetic acid and an ontogenic effect in infancy
J A Wolff, B Barshop, W L Nyhan, et al.
American Journal of Obstetrics and Gynecology
|
April 1, 1992
Maternal phenylketonuria collaborative study, obstetric aspects and outcome: the first 6 years
L D Platt, R Koch, C Azen, et al.
American Journal of Medical Genetics. Part A
|
January 7, 2023
Genomic sequencing in a cohort of individuals with fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) syndrome
Dena R Matalon, Elizabeth J Bhoj, Dong Li, et al.
Molecular Genetics and Metabolism
|
September 26, 2000
Maternal phenylketonuria: an international study
R Koch, W Hanley, H Levy, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement
|
December 1, 1994
The international collaborative study of maternal phenylketonuria: status report 1994
R Koch, H L Levy, R Matalon, et al.
European Journal of Pediatrics
|
July 1, 1996
Maternal non-phenylketonuric mild hyperphenylalaninemia
H L Levy, S E Waisbren, D Lobbregt, et al.
Page
of 19