isoleucine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

isoleucine has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Boyadjiev, S; Dlouhy, SR; Green, K; Hodes, ME; Pratt, VM	1
Conneally, PM; Dlouhy, SR; Hodes, ME; Pratt, VM; Schinzel, A; Trofatter, JA	1

Other Studies

2 other study(ies) available for isoleucine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

Article	Year
Pelizaeus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus. American journal of medical genetics, 1995, Jul-31, Volume: 58, Issue:1 Topics: Adult; Base Sequence; Deoxyribonucleases, Type II Site-Specific; Diffuse Cerebral Sclerosis of Schilder; DNA Primers; Exons; Family; Female; Genetic Markers; Humans; Infant, Newborn; Isoleucine; Male; Molecular Sequence Data; Myelin Proteolipid Protein; Point Mutation; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Threonine; X Chromosome	1995
A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease. American journal of medical genetics, 1991, Volume: 38, Issue:1 Topics: Diffuse Cerebral Sclerosis of Schilder; Exons; Female; Heterozygote; Humans; Isoleucine; Magnetic Resonance Imaging; Male; Mutation; Myelin Proteins; Myelin Proteolipid Protein; Pedigree; Threonine; X Chromosome	1991

Article

Year

Pelizaeus-Merzbacher disease caused by a de novo mutation that originated in exon 2 of the maternal great-grandfather of the propositus.

American journal of medical genetics, 1995, Jul-31, Volume: 58, Issue:1

Topics: Adult; Base Sequence; Deoxyribonucleases, Type II Site-Specific; Diffuse Cerebral Sclerosis of Schilder; DNA Primers; Exons; Family; Female; Genetic Markers; Humans; Infant, Newborn; Isoleucine; Male; Molecular Sequence Data; Myelin Proteolipid Protein; Point Mutation; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Threonine; X Chromosome

1995

A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease.

American journal of medical genetics, 1991, Volume: 38, Issue:1

Topics: Diffuse Cerebral Sclerosis of Schilder; Exons; Female; Heterozygote; Humans; Isoleucine; Magnetic Resonance Imaging; Male; Mutation; Myelin Proteins; Myelin Proteolipid Protein; Pedigree; Threonine; X Chromosome

1991