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

ornithine has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (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
Dlouhy, SR; Geraghty, MT; Hodes, ME; Naidu, S	1

Other Studies

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

Article	Year
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria. Journal of inherited metabolic disease, 1997, Volume: 20, Issue:6 Topics: Brain; Child, Preschool; Deoxyribonucleases, Type II Site-Specific; Diffuse Cerebral Sclerosis of Schilder; DNA; Genetic Linkage; Humans; Kidney; Lysine; Magnetic Resonance Imaging; Male; Mutation; Myelin Proteolipid Protein; Ornithine; Pedigree; Spastic Paraplegia, Hereditary; X Chromosome	1997

Article

Year

A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.

Journal of inherited metabolic disease, 1997, Volume: 20, Issue:6

Topics: Brain; Child, Preschool; Deoxyribonucleases, Type II Site-Specific; Diffuse Cerebral Sclerosis of Schilder; DNA; Genetic Linkage; Humans; Kidney; Lysine; Magnetic Resonance Imaging; Male; Mutation; Myelin Proteolipid Protein; Ornithine; Pedigree; Spastic Paraplegia, Hereditary; X Chromosome

1997