arginine and Niemann-Pick Disease, Type B

arginine has been researched along with Niemann-Pick Disease, Type B in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Aneja, A; Dalal, A; Sharma, A; Sondhi, V	1

Other Studies

1 other study(ies) available for arginine and Niemann-Pick Disease, Type B

Article	Year
R542X mutation in SMPD1 gene: genetically novel mutation with phenotypic features intermediate between type A and type B Niemann-Pick disease. BMJ case reports, 2012, Nov-27, Volume: 2012 Topics: Alleles; Amino Acid Substitution; Arginine; Codon, Terminator; DNA Mutational Analysis; Female; Fluorescein Angiography; Homozygote; Humans; Infant; Niemann-Pick Disease, Type A; Niemann-Pick Disease, Type B; Phenotype; Sphingomyelin Phosphodiesterase	2012

Article

Year

R542X mutation in SMPD1 gene: genetically novel mutation with phenotypic features intermediate between type A and type B Niemann-Pick disease.

BMJ case reports, 2012, Nov-27, Volume: 2012

Topics: Alleles; Amino Acid Substitution; Arginine; Codon, Terminator; DNA Mutational Analysis; Female; Fluorescein Angiography; Homozygote; Humans; Infant; Niemann-Pick Disease, Type A; Niemann-Pick Disease, Type B; Phenotype; Sphingomyelin Phosphodiesterase

2012