Search research articles
Contact Us
Filters
Showing results (681-690 of 694) with videos related to
Page
of 70
Sort By:
Journal of Inherited Metabolic Disease
|
June 17, 2015
Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
Stefan Kölker, Angeles Garcia Cazorla, Vassili Valayannopoulos, et al.
Physical Review Letters
|
June 26, 2026
Beta-Delayed Neutron Emission of N=84 ^{132}Cd
M Madurga, Z Y Xu, R Grzywacz, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
Stefan Kölker, Angeles Garcia-Cazorla, Angeles Garcia Cazorla, et al.
Journal of Inherited Metabolic Disease
|
February 12, 2019
Newborn screening for homocystinurias: Recent recommendations versus current practice
Rebecca Keller, Petr Chrastina, Markéta Pavlíková, et al.
Physical Review Letters
|
November 20, 2020
Competition between Allowed and First-Forbidden β Decay: The Case of ^{208}Hg→^{208}Tl
R J Carroll, Zs Podolyák, T Berry, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
Stefan Kölker, Vassili Valayannopoulos, Alberto B Burlina, et al.
Journal of Inherited Metabolic Disease
|
June 17, 2015
Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
Stefan Kölker, Vassili Valayannopoulos, Alberto B Burlina, et al.
Nature Communications
|
June 13, 2023
Immune resilience despite inflammatory stress promotes longevity and favorable health outcomes including resistance to infection
Sunil K Ahuja, Muthu Saravanan Manoharan, Grace C Lee, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2019
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry
Martina Huemer, Daria Diodato, Diego Martinelli, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
Paulien A Terhal, Rutger Jan A J Nievelstein, Eva J J Verver, et al.
Page
of 70
Search research articles
Search
Showing results (681-690 of 694) with videos related to
Sort By:
Page
of 70
Journal of Inherited Metabolic Disease
|
June 17, 2015
Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
Stefan Kölker, Angeles Garcia Cazorla, Vassili Valayannopoulos, et al.
Physical Review Letters
|
June 26, 2026
Beta-Delayed Neutron Emission of N=84 ^{132}Cd
M Madurga, Z Y Xu, R Grzywacz, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation
Stefan Kölker, Angeles Garcia-Cazorla, Angeles Garcia Cazorla, et al.
Journal of Inherited Metabolic Disease
|
February 12, 2019
Newborn screening for homocystinurias: Recent recommendations versus current practice
Rebecca Keller, Petr Chrastina, Markéta Pavlíková, et al.
Physical Review Letters
|
November 20, 2020
Competition between Allowed and First-Forbidden β Decay: The Case of ^{208}Hg→^{208}Tl
R J Carroll, Zs Podolyák, T Berry, et al.
Journal of Inherited Metabolic Disease
|
April 16, 2015
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
Stefan Kölker, Vassili Valayannopoulos, Alberto B Burlina, et al.
Journal of Inherited Metabolic Disease
|
June 17, 2015
Erratum to: The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype
Stefan Kölker, Vassili Valayannopoulos, Alberto B Burlina, et al.
Nature Communications
|
June 13, 2023
Immune resilience despite inflammatory stress promotes longevity and favorable health outcomes including resistance to infection
Sunil K Ahuja, Muthu Saravanan Manoharan, Grace C Lee, et al.
Journal of Inherited Metabolic Disease
|
February 19, 2019
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry
Martina Huemer, Daria Diodato, Diego Martinelli, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
A study of the clinical and radiological features in a cohort of 93 patients with a COL2A1 mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype
Paulien A Terhal, Rutger Jan A J Nievelstein, Eva J J Verver, et al.
Page
of 70