carnitine has been researched along with Infant, Newborn, Diseases in 12 studies
Infant, Newborn, Diseases: Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts.
| Excerpt | Relevance | Reference |
|---|---|---|
| "No further seizures were noted by day 5." | 5.51 | A newborn with seizures born to a mother diagnosed with primary carnitine deficiency. ( Chen, S; Hu, Y; Huang, Y; Lin, J; Lin, Z; Nan, Y; Zhou, X, 2019) |
| "Macrosomia is an interfering factor for the analytes C3 and C18:1, leading to higher risk of false-positive results for methylmalonic/propionic acidemia and carnitine palmitoyl transferase type 2 deficiency, respectively." | 3.96 | Neonatal Macrosomia is an Interfering Factor for Analytes on the Colorado State Newborn Screen. ( Baker, PR; Wright, EL, 2020) |
| "This disorder, known as phenylketonuria, produces profound mental retardation if not detected and treated early in life." | 2.43 | A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing. ( Chace, DH; Kalas, TA, 2005) |
| "No further seizures were noted by day 5." | 1.51 | A newborn with seizures born to a mother diagnosed with primary carnitine deficiency. ( Chen, S; Hu, Y; Huang, Y; Lin, J; Lin, Z; Nan, Y; Zhou, X, 2019) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (25.00) | 18.7374 |
| 1990's | 1 (8.33) | 18.2507 |
| 2000's | 1 (8.33) | 29.6817 |
| 2010's | 5 (41.67) | 24.3611 |
| 2020's | 2 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bower, A | 1 |
| Imbard, A | 1 |
| Benoist, JF | 1 |
| Pichard, S | 1 |
| Rigal, O | 1 |
| Baud, O | 1 |
| Schiff, M | 1 |
| Liu, Q | 1 |
| Yin, A | 1 |
| Wen, S | 1 |
| Shi, X | 1 |
| Fang, L | 1 |
| Rao, T | 1 |
| Liang, J | 1 |
| Wu, J | 1 |
| Wright, EL | 1 |
| Baker, PR | 1 |
| Chen, S | 2 |
| Hu, Y | 1 |
| Huang, Y | 1 |
| Nan, Y | 1 |
| Zhou, X | 1 |
| Lin, J | 1 |
| Lin, Z | 1 |
| Zhao, D | 1 |
| Han, L | 1 |
| He, Z | 1 |
| Zhang, J | 1 |
| Zhang, Y | 1 |
| El-Hattab, AW | 1 |
| Li, FY | 1 |
| Shen, J | 1 |
| Powell, BR | 1 |
| Bawle, EV | 1 |
| Adams, DJ | 1 |
| Wahl, E | 1 |
| Kobori, JA | 1 |
| Graham, B | 1 |
| Scaglia, F | 1 |
| Wong, LJ | 1 |
| Kirmse, B | 1 |
| Hobbs, CV | 1 |
| Peter, I | 1 |
| Laplante, B | 1 |
| Caggana, M | 1 |
| Kloke, K | 1 |
| Raymond, K | 1 |
| Summar, M | 1 |
| Borkowsky, W | 1 |
| Chace, DH | 1 |
| Kalas, TA | 1 |
| Orzali, A | 2 |
| Donzelli, F | 2 |
| Enzi, G | 1 |
| Rubaltelli, FF | 2 |
| Maetzke, G | 1 |
| Lipsky, CL | 1 |
| Spear, ML | 1 |
| Zlotkin, SH | 1 |
| Stallings, VA | 1 |
| Pencharz, PB | 1 |
3 reviews available for carnitine and Infant, Newborn, Diseases
| Article | Year |
|---|---|
A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.
Topics: Amino Acids; Carnitine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Spectrometry; Metab | 2005 |
Recent advances in parenteral nutrition.
Topics: Carnitine; Fat Emulsions, Intravenous; Humans; Infant Nutritional Physiological Phenomena; Infant, L | 1995 |
Total parenteral nutrition in children.
Topics: Adolescent; Amino Acids; Biotin; Carnitine; Child; Child, Preschool; Copper; Humans; Infant; Infant | 1985 |
9 other studies available for carnitine and Infant, Newborn, Diseases
| Article | Year |
|---|---|
Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
Topics: Amino Acids; Carnitine; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intensiv | 2019 |
Analysis of amino acids and acylcarnitines profiles in small, appropriate, and large for gestational age neonates.
Topics: Amino Acids; Birth Weight; Carnitine; Gestational Age; Humans; Infant, Newborn; Infant, Newborn, Dis | 2022 |
Neonatal Macrosomia is an Interfering Factor for Analytes on the Colorado State Newborn Screen.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Carnitine; Carnitine O-Palmitoyltransferase; Colorado; | 2020 |
A newborn with seizures born to a mother diagnosed with primary carnitine deficiency.
Topics: Brain; Cardiomyopathies; Carnitine; Electroencephalography; Female; Fetal Diseases; Humans; Hyperamm | 2019 |
Identification of the plasma metabolomics as early diagnostic markers between biliary atresia and neonatal hepatitis syndrome.
Topics: Amino Acids; Biliary Atresia; Biomarkers; Carnitine; Chromatography, Liquid; Demography; Discriminan | 2014 |
Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspects.
Topics: Adult; Carnitine; Child, Preschool; Family; Female; Humans; Infant; Infant, Newborn; Infant, Newborn | 2010 |
Abnormal newborn screens and acylcarnitines in HIV-exposed and ARV-exposed infants.
Topics: Anti-Retroviral Agents; Carnitine; Case-Control Studies; HIV Infections; Humans; Infant, Newborn; In | 2013 |
Effect of carnitine on lipid metabolism in the newborn. I. Carnitine supplementation during total parenteral nutrition in the first 48 hours of life.
Topics: Carnitine; Fat Emulsions, Intravenous; Humans; Infant, Newborn; Infant, Newborn, Diseases; Ketone Bo | 1983 |
Effect of carnitine on lipid metabolism in the neonate. II. Carnitine addition to lipid infusion during prolonged total parenteral nutrition.
Topics: 3-Hydroxybutyric Acid; Carnitine; Fat Emulsions, Intravenous; Fatty Acids, Nonesterified; Humans; Hy | 1984 |