tyrosine and Amylopectinosis

tyrosine has been researched along with Amylopectinosis in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (25.00)	18.7374
1990's	2 (50.00)	18.2507
2000's	1 (25.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abbey, CA; Adelson, DL; Binns, MM; Mickelson, JR; Valberg, SJ; Ward, TL	1
Honnda, K; Inamoto, T; Tanaka, K; Tokunaga, Y; Uemoto, S; Yamaoka, Y	1
Kumada, S; Okaniwa, M	1
Dimmick, JE; Hardwick, DF	1

Reviews

2 review(s) available for tyrosine and Amylopectinosis

Article	Year
[Progressive neuronal degeneration and childhood cirrhosis]. Ryoikibetsu shokogun shirizu, 1995, Issue:8 Topics: Galactosemias; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Metabolism, Inborn Errors; Peripheral Nervous System Diseases; Tyrosine	1995
Metabolic cirrhoses of infancy and early childhood. Perspectives in pediatric pathology, 1976, Volume: 3 Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine	1976

Article

Year

[Progressive neuronal degeneration and childhood cirrhosis].

Ryoikibetsu shokogun shirizu, 1995, Issue:8

Topics: Galactosemias; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Cirrhosis; Metabolism, Inborn Errors; Peripheral Nervous System Diseases; Tyrosine

1995

Metabolic cirrhoses of infancy and early childhood.

Perspectives in pediatric pathology, 1976, Volume: 3

Topics: Amino Acid Metabolism, Inborn Errors; Cystic Fibrosis; Cystinosis; Fructose Intolerance; Galactosemias; Genetics, Medical; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Iatrogenic Disease; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Liver; Liver Cirrhosis; Metabolism, Inborn Errors; Mucopolysaccharidoses; Niemann-Pick Diseases; Polycystic Kidney Diseases; Tyrosine

1976

Other Studies

2 other study(ies) available for tyrosine and Amylopectinosis

Article	Year
Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV. Mammalian genome : official journal of the International Mammalian Genome Society, 2004, Volume: 15, Issue:7 Topics: 1,4-alpha-Glucan Branching Enzyme; Alleles; Animals; Base Sequence; Codon; Codon, Terminator; DNA; DNA Mutational Analysis; DNA, Complementary; Exons; Genes, Recessive; Genotype; Glycogen Storage Disease Type IV; Homozygote; Horses; Humans; Molecular Sequence Data; Mutation; Polysaccharides; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tyrosine	2004
Living-related liver transplantation for inborn errors of metabolism. Transplantation proceedings, 1994, Volume: 26, Issue:4 Topics: Adolescent; Adult; Child; Child, Preschool; Fathers; Female; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Transplantation; Male; Metabolism, Inborn Errors; Mothers; Porphyria, Hepatoerythropoietic; Survival Rate; Tissue Donors; Tyrosine	1994

Article

Year

Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV.

Mammalian genome : official journal of the International Mammalian Genome Society, 2004, Volume: 15, Issue:7

Topics: 1,4-alpha-Glucan Branching Enzyme; Alleles; Animals; Base Sequence; Codon; Codon, Terminator; DNA; DNA Mutational Analysis; DNA, Complementary; Exons; Genes, Recessive; Genotype; Glycogen Storage Disease Type IV; Homozygote; Horses; Humans; Molecular Sequence Data; Mutation; Polysaccharides; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tyrosine

2004

Transplantation proceedings, 1994, Volume: 26, Issue:4

Topics: Adolescent; Adult; Child; Child, Preschool; Fathers; Female; Glycogen Storage Disease Type IV; Hepatolenticular Degeneration; Humans; Infant; Liver Transplantation; Male; Metabolism, Inborn Errors; Mothers; Porphyria, Hepatoerythropoietic; Survival Rate; Tissue Donors; Tyrosine

1994