proline and Cerebral Pseudosclerosis

proline has been researched along with Cerebral Pseudosclerosis in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	1 (33.33)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Correa, G; Lopera, F; Moreno, S; Ramírez-Gomez, L; Rio, MJ; Velez-Pardo, C	1
Chang, JG; Jong, YJ; Lee, CC; Lin, SP; Lo, MC; Tsai, CH; Tsai, FJ; Wu, JY; Yang, CF	1
Greco, GM; Magli, A	1

Reviews

1 review(s) available for proline and Cerebral Pseudosclerosis

Article	Year
[Eye manifestations of amino acid disorders]. Minerva pediatrica, 1978, May-31, Volume: 30, Issue:10 Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates	1978

Article

Year

[Eye manifestations of amino acid disorders].

Minerva pediatrica, 1978, May-31, Volume: 30, Issue:10

Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates

1978

Other Studies

2 other study(ies) available for proline and Cerebral Pseudosclerosis

Article	Year
New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred. Neuroscience letters, 2004, Sep-09, Volume: 367, Issue:3 Topics: Adenosine Triphosphatases; Adolescent; Adult; Cation Transport Proteins; Colombia; Copper-Transporting ATPases; DNA Mutational Analysis; Exons; Female; Founder Effect; Hepatolenticular Degeneration; Humans; Male; Molecular Sequence Data; Mutation; Polymorphism, Single-Stranded Conformational; Proline; Threonine	2004
Mutation analysis of Wilson disease in Taiwan and description of six new mutations. Human mutation, 1998, Volume: 12, Issue:6 Topics: Alleles; Alternative Splicing; Amino Acid Substitution; Arginine; Aspartic Acid; DNA; DNA Mutational Analysis; Glutamine; Glycine; Hepatolenticular Degeneration; Humans; Leucine; Leukocytes; Mutation; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Proline; Taiwan	1998

Article

Year

New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred.

Neuroscience letters, 2004, Sep-09, Volume: 367, Issue:3

Topics: Adenosine Triphosphatases; Adolescent; Adult; Cation Transport Proteins; Colombia; Copper-Transporting ATPases; DNA Mutational Analysis; Exons; Female; Founder Effect; Hepatolenticular Degeneration; Humans; Male; Molecular Sequence Data; Mutation; Polymorphism, Single-Stranded Conformational; Proline; Threonine

2004

Mutation analysis of Wilson disease in Taiwan and description of six new mutations.

Human mutation, 1998, Volume: 12, Issue:6

Topics: Alleles; Alternative Splicing; Amino Acid Substitution; Arginine; Aspartic Acid; DNA; DNA Mutational Analysis; Glutamine; Glycine; Hepatolenticular Degeneration; Humans; Leucine; Leukocytes; Mutation; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Proline; Taiwan

1998