citrulline and Carbamoyl-Phosphate Synthase I Deficiency Disease

citrulline has been researched along with Carbamoyl-Phosphate Synthase I Deficiency Disease in 3 studies

Research

Studies (3)

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	2 (66.67)	24.3611
2020's	1 (33.33)	2.80

Authors

Authors	Studies
Burlina, AB; Cazzorla, C; Commone, A; Gragnaniello, V; Gueraldi, D; Häberle, J; Loro, C; Puma, A	1
Cynober, L; Forbes, A; Osowska, S; Papadia, C	1
Mhanni, AA; Prasad, C; Rockman-Greenberg, C	1

Reviews

1 review(s) available for citrulline and Carbamoyl-Phosphate Synthase I Deficiency Disease

Article	Year
Citrulline in health and disease. Review on human studies. Clinical nutrition (Edinburgh, Scotland), 2018, Volume: 37, Issue:6 Pt A Topics: Anabolic Agents; Animals; Arginine; Athletic Performance; Carbamoyl-Phosphate Synthase I Deficiency Disease; Cardiovascular Diseases; Citrulline; Endothelial Cells; Enterocytes; Female; Humans; Immunity; Male; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Oxidative Stress; Protein Biosynthesis; Urea Cycle Disorders, Inborn	2018

Article

Year

Citrulline in health and disease. Review on human studies.

Clinical nutrition (Edinburgh, Scotland), 2018, Volume: 37, Issue:6 Pt A

Topics: Anabolic Agents; Animals; Arginine; Athletic Performance; Carbamoyl-Phosphate Synthase I Deficiency Disease; Cardiovascular Diseases; Citrulline; Endothelial Cells; Enterocytes; Female; Humans; Immunity; Male; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Oxidative Stress; Protein Biosynthesis; Urea Cycle Disorders, Inborn

2018

Other Studies

2 other study(ies) available for citrulline and Carbamoyl-Phosphate Synthase I Deficiency Disease

Article	Year
Variant in the allosteric domain of CPS1 protein associated with effectiveness of N-carbamoyl glutamate therapy in neonatal onset CPS1 deficiency. Journal of pediatric endocrinology & metabolism : JPEM, 2023, Sep-26, Volume: 36, Issue:9 Topics: Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency Disease; Citrulline; Glutamic Acid; Humans; Infant, Newborn; Urea Cycle Disorders, Inborn	2023
Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood. Pediatric emergency care, 2011, Volume: 27, Issue:9 Topics: Abdominal Pain; Alkalosis, Respiratory; Arginine; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child, Preschool; Citrulline; Consciousness Disorders; Diagnosis, Differential; Diet, Protein-Restricted; Emergencies; Exons; Female; Glutamine; Humans; Hyperammonemia; Language Development Disorders; Liver Transplantation; Mutation, Missense; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Recurrence	2011

Article

Year

Variant in the allosteric domain of CPS1 protein associated with effectiveness of N-carbamoyl glutamate therapy in neonatal onset CPS1 deficiency.

Journal of pediatric endocrinology & metabolism : JPEM, 2023, Sep-26, Volume: 36, Issue:9

Topics: Carbamoyl-Phosphate Synthase (Ammonia); Carbamoyl-Phosphate Synthase I Deficiency Disease; Citrulline; Glutamic Acid; Humans; Infant, Newborn; Urea Cycle Disorders, Inborn

2023

Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood.

Pediatric emergency care, 2011, Volume: 27, Issue:9

Topics: Abdominal Pain; Alkalosis, Respiratory; Arginine; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child, Preschool; Citrulline; Consciousness Disorders; Diagnosis, Differential; Diet, Protein-Restricted; Emergencies; Exons; Female; Glutamine; Humans; Hyperammonemia; Language Development Disorders; Liver Transplantation; Mutation, Missense; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Recurrence

2011