glutamic acid and Jaundice, Neonatal

glutamic acid has been researched along with Jaundice, Neonatal in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	1 (50.00)	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
KUMAR, S; SACHAR, RS; SINGH, H; SINGH, ID; WIG, KL	1
Brabec, V; Jarolim, P; Palek, J; Rubin, HL	1

Other Studies

2 other study(ies) available for glutamic acid and Jaundice, Neonatal

Article	Year
BLOOD AND CEREBROSPINAL FLUID AMMONIA AND GLUTATHIONE LEVELS IN LIVER DISEASE, AND THE EFFECT OF INTRAVENOUS GLUTAMATE ON THESE LEVELS. The Indian journal of medical research, 1963, Volume: 51 Topics: Ammonia; Anemia; Blood Chemical Analysis; Cerebrospinal Fluid; Child; Glutamates; Glutamic Acid; Glutathione; Hepatic Encephalopathy; Hepatitis; Hepatitis A; Humans; Hypersplenism; Injections, Intravenous; Jaundice; Jaundice, Neonatal; Jaundice, Obstructive; Liver Cirrhosis; Liver Diseases; Neurologic Manifestations	1963
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis. The Journal of clinical investigation, 1995, Volume: 95, Issue:3 Topics: Abnormalities, Multiple; Alleles; Alternative Splicing; Ankyrins; Base Sequence; Erythrocyte Membrane; Erythrocytes, Abnormal; Genes, Dominant; Glutamic Acid; Humans; Infant; Infant, Newborn; Jaundice, Neonatal; Molecular Sequence Data; Mutation; Osmotic Fragility; RNA, Messenger; Spectrin	1995

Article

Year

BLOOD AND CEREBROSPINAL FLUID AMMONIA AND GLUTATHIONE LEVELS IN LIVER DISEASE, AND THE EFFECT OF INTRAVENOUS GLUTAMATE ON THESE LEVELS.

The Indian journal of medical research, 1963, Volume: 51

Topics: Ammonia; Anemia; Blood Chemical Analysis; Cerebrospinal Fluid; Child; Glutamates; Glutamic Acid; Glutathione; Hepatic Encephalopathy; Hepatitis; Hepatitis A; Humans; Hypersplenism; Injections, Intravenous; Jaundice; Jaundice, Neonatal; Jaundice, Obstructive; Liver Cirrhosis; Liver Diseases; Neurologic Manifestations

1963

A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis.

The Journal of clinical investigation, 1995, Volume: 95, Issue:3

Topics: Abnormalities, Multiple; Alleles; Alternative Splicing; Ankyrins; Base Sequence; Erythrocyte Membrane; Erythrocytes, Abnormal; Genes, Dominant; Glutamic Acid; Humans; Infant; Infant, Newborn; Jaundice, Neonatal; Molecular Sequence Data; Mutation; Osmotic Fragility; RNA, Messenger; Spectrin

1995