arginine and Absence of Corpus Callosum

arginine has been researched along with Absence of Corpus Callosum in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Chitayat, D; Fransen, E; Holden, JJ; Van Camp, G; Vits, L; Willems, PJ	1
Abe, K; Hayashi, T; Iwatsuki, K; Manabe, Y; Matsubara, E; Murakami, T; Nagano, I; Sato, K; Shoji, M	1

Other Studies

2 other study(ies) available for arginine and Absence of Corpus Callosum

Article	Year
Evidence for somatic and germline mosaicism in CRASH syndrome. Human mutation, 1998, Volume: Suppl 1 Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Amino Acid Substitution; Arginine; DNA; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; Germ-Line Mutation; Humans; Hydrocephalus; Intellectual Disability; Leukocyte L1 Antigen Complex; Male; Membrane Glycoproteins; Mosaicism; Mutation; Neural Cell Adhesion Molecules; Pedigree; Polymorphism, Single-Stranded Conformational; Proline; Spastic Paraplegia, Hereditary; Thumb; X Chromosome	1998
Two Japanese CADASIL families with a R141C mutation in the Notch3 gene. Internal medicine (Tokyo, Japan), 2001, Volume: 40, Issue:11 Topics: Agenesis of Corpus Callosum; Arginine; Cysteine; Dementia, Multi-Infarct; DNA Mutational Analysis; Female; Humans; Middle Aged; Mutation, Missense; Pedigree; Point Mutation; Polymerase Chain Reaction; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch	2001

Article

Year

Evidence for somatic and germline mosaicism in CRASH syndrome.

Human mutation, 1998, Volume: Suppl 1

Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Amino Acid Substitution; Arginine; DNA; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; Germ-Line Mutation; Humans; Hydrocephalus; Intellectual Disability; Leukocyte L1 Antigen Complex; Male; Membrane Glycoproteins; Mosaicism; Mutation; Neural Cell Adhesion Molecules; Pedigree; Polymorphism, Single-Stranded Conformational; Proline; Spastic Paraplegia, Hereditary; Thumb; X Chromosome

1998

Two Japanese CADASIL families with a R141C mutation in the Notch3 gene.

Internal medicine (Tokyo, Japan), 2001, Volume: 40, Issue:11

Topics: Agenesis of Corpus Callosum; Arginine; Cysteine; Dementia, Multi-Infarct; DNA Mutational Analysis; Female; Humans; Middle Aged; Mutation, Missense; Pedigree; Point Mutation; Polymerase Chain Reaction; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch

2001