tyrosine and Glycogen Storage Disease Type II

tyrosine has been researched along with Glycogen Storage Disease Type II in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kiuru-Enari, SM; Korpela, MP; Lamminen, AE; Löfberg, MI; Paetau, A; Timonen, MH	1
Allende, H; Boix-Ochoa, J; Infante, D; Margarit, C; Martínez Ibáñez, V; Sanchís, L; Tormo, R	1

Other Studies

2 other study(ies) available for tyrosine and Glycogen Storage Disease Type II

Article	Year
A novel mutation of the GAA gene in a Finnish late-onset Pompe disease patient: clinical phenotype and follow-up with enzyme replacement therapy. Muscle & nerve, 2009, Volume: 40, Issue:1 Topics: alpha-Glucosidases; DNA Mutational Analysis; Electrocardiography; Electromyography; Electrons; Female; Finland; Follow-Up Studies; Glycogen Storage Disease Type II; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Muscle, Skeletal; Mutation; Radionuclide Imaging; Recombinant Proteins; Tyrosine; Young Adult	2009
[New perspectives in liver-based metabolic errors: liver transplantation]. Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica, 1989, Volume: 2, Issue:3 Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycogen Storage Disease Type II; Humans; Hyperlipoproteinemia Type II; Infant, Newborn; Liver; Liver Cirrhosis; Liver Transplantation; Male; Metabolism, Inborn Errors; Tyrosine	1989

Article

Year

A novel mutation of the GAA gene in a Finnish late-onset Pompe disease patient: clinical phenotype and follow-up with enzyme replacement therapy.

Muscle & nerve, 2009, Volume: 40, Issue:1

Topics: alpha-Glucosidases; DNA Mutational Analysis; Electrocardiography; Electromyography; Electrons; Female; Finland; Follow-Up Studies; Glycogen Storage Disease Type II; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Muscle, Skeletal; Mutation; Radionuclide Imaging; Recombinant Proteins; Tyrosine; Young Adult

2009

[New perspectives in liver-based metabolic errors: liver transplantation].

Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica, 1989, Volume: 2, Issue:3

Topics: alpha 1-Antitrypsin Deficiency; Amino Acid Metabolism, Inborn Errors; Child; Female; Glycogen Storage Disease Type II; Humans; Hyperlipoproteinemia Type II; Infant, Newborn; Liver; Liver Cirrhosis; Liver Transplantation; Male; Metabolism, Inborn Errors; Tyrosine

1989