citrulline has been researched along with Infant, Newborn, Diseases in 19 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (68.42) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (5.26) | 29.6817 |
| 2010's | 3 (15.79) | 24.3611 |
| 2020's | 2 (10.53) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, Y; Jiang, M; Li, X; Lin, Y; Liu, L; Liu, Z; Lu, Z; Peng, M; Shao, Y; Zhang, W | 1 |
| Bos, AF; Derikx, JPM; Feenstra, FA; Heiner-Fokkema, MR; Hulscher, JBF; Kooi, EMW; Kuik, SJ | 1 |
| Betancourt, LR; Ceballos, GA; Contreras, MT; Gallardo, MJ; Hernandez, LE; Hernandez, LF; Rada, PV | 1 |
| Kobayashi, K; Ngu, HL; Zabedah, MY | 1 |
| Augoustides-Savvopoulou, P; Diamanti, E; Drossou-Agakidou, V; Ioannou, HP; Piretzi, K | 1 |
| Begum, L; Gao, HZ; Iijima, M; Jalil, MA; Kobayashi, K; Li, MX; Nishi, I; Saheki, T; Yamaguchi, N; Yasuda, T | 1 |
| COFFEY, VP | 1 |
| Charpentier, C; Coude, FX; Marsac, C; Munnich, A; Ogier, H; Saudubray, JM | 1 |
| Canosa, C; Grisolia, S; Gutierez, F; Jordá, A; Nyhan, WL; Rubio, V | 1 |
| Bost, M; Favier, A; Frappat, P; Grandgeorges, D; Joannard, A; Plasse, M; Serre, JC | 1 |
| Briand, P; Cathelineau, L; Kamoun, P; Pham Dinh, D | 1 |
| Batshaw, M; Brusilow, S; Robinson, B; Sherwood, G; Walser, M | 1 |
| Shih, VE | 1 |
| Brechbühler, T; Colombo, JP; Signer, E; Wick, H | 1 |
| Bachmann, C; Baumgartner, R; Brechbühler, T; Colombo, JP; Mihatsch, MJ; Ohnacker, H; Wick, H; Wiesmann, U | 1 |
| Bachmann, C; Mihatsch, MJ; Ohnacker, H; Riede, UN; Wick, H | 1 |
| Danks, DM | 1 |
| Danks, DM; Tippett, P; Zentner, G | 1 |
| Hommes, FA; Monnens, LA; Schretlen, ED; Trijbels, JM; Van Der Zee, SP | 1 |
1 review(s) available for citrulline and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Pathogenesis and pathophysiology of citrin (a mitochondrial aspartate glutamate carrier) deficiency.
Topics: Calcium-Binding Proteins; Cholestasis, Intrahepatic; Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Membrane Transport Proteins; Metabolism, Inborn Errors; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Mutation; Organic Anion Transporters | 2002 |
18 other study(ies) available for citrulline and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Features of liver injury in 138 Chinese patients with NICCD.
Topics: Cholestasis, Intrahepatic; Citrulline; Citrullinemia; East Asian People; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mitochondrial Membrane Transport Proteins; Mutation; Tyrosine | 2023 |
Plasma citrulline during the first 48 h after onset of necrotizing enterocolitis in preterm infants.
Topics: Adult; Citrulline; Enteral Nutrition; Enterocolitis, Necrotizing; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature | 2021 |
Correlation between plasma levels of arginine and citrulline in preterm and full-term neonates: Therapeutical implications.
Topics: Arginine; Citrulline; Cohort Studies; Electrophoresis, Capillary; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Infant, Premature, Diseases; Male; Nitric Oxide; Spectrometry, Fluorescence | 2017 |
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in three Malay children.
Topics: Child; Child, Preschool; Cholestasis, Intrahepatic; Citrulline; Citrullinemia; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Malaysia; Male; Mitochondrial Membrane Transport Proteins; Mutagenesis, Insertional; Polymerase Chain Reaction | 2010 |
Plasma citrulline levels in preterm neonates with necrotizing enterocolitis.
Topics: Amino Acids; Birth Weight; Case-Control Studies; Citrulline; Enterocolitis, Necrotizing; Female; Gestational Age; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Male; Parenteral Nutrition; Prognosis; Sensitivity and Specificity | 2012 |
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency | 1964 |
Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.
Topics: Ammonia; Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Pyruvate Carboxylase Deficiency Disease | 1981 |
Transient hyperammonemias in infants with and without organic acidemia.
Topics: Acetyltransferases; Amino Acid Metabolism, Inborn Errors; Amino-Acid N-Acetyltransferase; Ammonia; Arginine; Carbamoyl-Phosphate Synthase (Ammonia); Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Time Factors; Urea | 1982 |
[Severe neonatal type of citrullinemia. Difficulties to expose heterozygotic state. Advantage of prenatal diagnosis (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Citrulline; Genetic Carrier Screening; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Prenatal Diagnosis | 1980 |
Studies on complementation in argininosuccinate synthetase and argininosuccinate lyase deficiencies in human fibroblasts.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Argininosuccinate Synthase; Argininosuccinic Acid; Argininosuccinic Aciduria; Cell Line; Citrulline; Female; Fibroblasts; Genetic Complementation Test; Humans; Infant, Newborn; Infant, Newborn, Diseases; Ligases; Lyases; Male; Polyethylene Glycols | 1981 |
Nitrogen metabolism in neonatal citrullinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Nitrogen; Ornithine; Urea | 1977 |
Congenital hyperammonemic syndromes.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase (Ammonia); Citrulline; Diagnosis, Differential; Humans; Hyperargininemia; Infant, Newborn; Infant, Newborn, Diseases; Lysine; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Syndrome; Urea | 1976 |
Citrullinemia in a newborn infant.
Topics: Amino Acid Metabolism, Inborn Errors; Chromatography; Citrulline; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male | 1972 |
Variants of citrullinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Brain; Chromatography; Citrulline; Dyspnea; Edema; Electrophoresis; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Lung; Male; Microscopy, Electron; Spasm; Urea | 1973 |
Liver morphology in a case of citrullinemia (a light and electron microscopic study).
Topics: Citrulline; Fatty Liver; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Male; Metabolism, Inborn Errors; Microscopy, Electron; Necrosis | 1974 |
Management of newborn babies in whom serious metabolic illness is anticipated.
Topics: Amino Acid Metabolism, Inborn Errors; Blood; Blood Protein Electrophoresis; Citrulline; Dietary Carbohydrates; Electrophoresis; Exchange Transfusion, Whole Blood; Female; Glucose; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Infusions, Parenteral; Labor, Induced; Metabolism, Inborn Errors; Patient Care Planning; Pregnancy; Umbilical Cord | 1974 |
Severe neonatal citrullinaemia.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Citrulline; Dietary Carbohydrates; Dietary Proteins; Glucose; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Male; Seizures; Urea | 1974 |
Citrullinaemia with rapidly fatal neonatal course.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Brain; Citrulline; Electrophoresis; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases; Ligases; Liver; Respiratory Insufficiency; Seizures | 1971 |