lysine has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 2 studies
| 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 | Studies |
|---|---|
| Dlouhy, SR; Hodes, ME; Marks, HG; Naidu, S; Pratt, VM | 1 |
| Dlouhy, SR; Geraghty, MT; Hodes, ME; Naidu, S | 1 |
2 other study(ies) available for lysine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis
| Article | Year |
|---|---|
A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher disease.
Topics: Amino Acid Sequence; Asparagine; Base Sequence; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; DNA Primers; Exons; Female; Humans; Lysine; Male; Molecular Sequence Data; Myelin Proteins; Myelin Proteolipid Protein; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic | 1995 |
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuria.
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 |