-
2
-
-
0028811213
-
Carnitine in neonatal nutrition
-
Borum PR Carnitine in neonatal nutrition J Child Neurol 10 Suppl 2 1995 2S25 2S31
-
(1995)
J Child Neurol
, vol.10
, Issue.Suppl 2
, pp. 2S25-2S31
-
-
Borum, PR1
-
3
-
-
0025561023
-
Primary and secondary disorders of carnitine metabolism
-
De Vivo DC Tein I Primary and secondary disorders of carnitine metabolism Int Pediatr 5 1990 134 141
-
(1990)
Int Pediatr
, vol.5
, pp. 134-141
-
-
De Vivo, DC1
Tein, I2
-
4
-
-
0027055939
-
Clinical and biochemical aspects of carnitine deficiency and insufficiency: Transport defects and inborn errors of β-oxidation
-
Angelini C Vergani L Martinuzzi A Clinical and biochemical aspects of carnitine deficiency and insufficiency: Transport defects and inborn errors of β-oxidation Crit Rev Clin Lab Sci 29 1992 217 242
-
(1992)
Crit Rev Clin Lab Sci
, vol.29
, pp. 217-242
-
-
Angelini, C1
Vergani, L2
Martinuzzi, A3
-
5
-
-
0028850504
-
Primary and secondary carnitine deficiency
-
Pons R De Vivo DC Primary and secondary carnitine deficiency J Child Neurol 10 Suppl 2 1995 2S8 2S24
-
(1995)
J Child Neurol
, vol.10
, Issue.Suppl 2
, pp. 2S8-2S24
-
-
Pons, R1
De Vivo, DC2
-
6
-
-
0028823795
-
Biosynthesis and metabolism of carnitine
-
Carter AL Abney TO Lapp DF Biosynthesis and metabolism of carnitine J Child Neurol 10 Suppl 2 1995 2S3 2S7
-
(1995)
J Child Neurol
, vol.10
, Issue.Suppl 2
, pp. 2S3-2S7
-
-
Carter, AL1
Abney, TO2
Lapp, DF3
-
7
-
-
0015215623
-
Protein methylation
-
Paik WK Kim S Protein methylation Science 174 1971 114 119
-
(1971)
Science
, vol.174
, pp. 114-119
-
-
Paik, WK1
Kim, S2
-
8
-
-
0019310364
-
Tissue distribution of carnitine biosynthetic enzymes in man
-
Rebouche CJ Engel AG Tissue distribution of carnitine biosynthetic enzymes in man Biochim Biophys Acta 630 1980 22 29
-
(1980)
Biochim Biophys Acta
, vol.630
, pp. 22-29
-
-
Rebouche, CJ1
Engel, AG2
-
9
-
-
0023267854
-
γ-Butyrobetaine hydroxylase activity is not rate limiting for carnitine biosynthesis in the human infant
-
Olson AL Rebouche CJ γ-Butyrobetaine hydroxylase activity is not rate limiting for carnitine biosynthesis in the human infant J Nutr 117 1987 1024 1031
-
(1987)
J Nutr
, vol.117
, pp. 1024-1031
-
-
Olson, AL1
Rebouche, CJ2
-
10
-
-
0030008232
-
Generation of hydroxy-trimethyllysine from trimethyllysine limits the carnitine biosynthesis in premature infants
-
Melegh B Hermann R Bock I Generation of hydroxy-trimethyllysine from trimethyllysine limits the carnitine biosynthesis in premature infants Acta Paediatr 85 1996 345 350
-
(1996)
Acta Paediatr
, vol.85
, pp. 345-350
-
-
Melegh, B1
Hermann, R2
Bock, I3
-
11
-
-
0022560507
-
ε-N-trimethyllysine availability regulates the rate of carnitine biosynthesis in the growing rat
-
Rebouche CJ Lehman LJ Olso AL ε-N-trimethyllysine availability regulates the rate of carnitine biosynthesis in the growing rat J Nutr 116 1986 751 759
-
(1986)
J Nutr
, vol.116
, pp. 751-759
-
-
Rebouche, CJ1
Lehman, LJ2
Olso, AL3
-
12
-
-
0030590877
-
Decreased plasma carnitine and trimethyl-l-lysine levels associated with lysosomal accumulation of a trimethyl-l-lysine containing protein in Batten disease
-
Katz ML Decreased plasma carnitine and trimethyl- l -lysine levels associated with lysosomal accumulation of a trimethyl- l -lysine containing protein in Batten disease Biochim Biophys Acta 1317 1996 192 198
-
(1996)
Biochim Biophys Acta
, vol.1317
, pp. 192-198
-
-
Katz, ML1
-
13
-
-
0030754261
-
Dietary carnitine supplements slow disease progression in a putative mouse model for hereditary ceroid lipofucsinosis
-
Katz ML Rice LM Gao CL Dietary carnitine supplements slow disease progression in a putative mouse model for hereditary ceroid lipofucsinosis J Neurosci Res 50 1977 123 132
-
(1977)
J Neurosci Res
, vol.50
, pp. 123-132
-
-
Katz, ML1
Rice, LM2
Gao, CL3
-
14
-
-
0021853230
-
Transfer and metabolism of carnitine and carnitine esters in the in vitro perfused human placenta
-
Schmidt-Sommerfeld E Penn D Sodha RJ Transfer and metabolism of carnitine and carnitine esters in the in vitro perfused human placenta Pediatr Res 19 1985 700 706
-
(1985)
Pediatr Res
, vol.19
, pp. 700-706
-
-
Schmidt-Sommerfeld, E1
Penn, D2
Sodha, RJ3
-
16
-
-
0031453511
-
Comparative study of plasma carnitine: Determination in the neonate and in normal delivery
-
Koumantakis E Evageliou A Sifakis S Comparative study of plasma carnitine: Determination in the neonate and in normal delivery Clin Exp Obstet Gynecol 24 1997 174 177
-
(1997)
Clin Exp Obstet Gynecol
, vol.24
, pp. 174-177
-
-
Koumantakis, E1
Evageliou, A2
Sifakis, S3
-
17
-
-
0019363702
-
Carnitine in the perinatal metabolism of lipids. I. Relationship between maternal and fetal plasma levels of carnitine and acylcarnitines
-
Novak M Monkus EF Chung D Carnitine in the perinatal metabolism of lipids. I. Relationship between maternal and fetal plasma levels of carnitine and acylcarnitines Pediatrics 67 1981 95 100
-
(1981)
Pediatrics
, vol.67
, pp. 95-100
-
-
Novak, M1
Monkus, EF2
Chung, D3
-
18
-
-
0019214324
-
Plasma and urine carnitine levels during development
-
Battistella PA Vergani L Donzelli F Plasma and urine carnitine levels during development Pediatr Res 14 1980 1379 1384
-
(1980)
Pediatr Res
, vol.14
, pp. 1379-1384
-
-
Battistella, PA1
Vergani, L2
Donzelli, F3
-
19
-
-
0020611578
-
Carnitine status at birth of newborn infants of varying gestation
-
Shenai JP Borum PR Mohan P Carnitine status at birth of newborn infants of varying gestation Pediatr Res 17 1983 579 582
-
(1983)
Pediatr Res
, vol.17
, pp. 579-582
-
-
Shenai, JP1
Borum, PR2
Mohan, P3
-
20
-
-
0021362187
-
Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes
-
Rebouche CJ Engel AG Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes J Clin Invest 73 1984 857 867
-
(1984)
J Clin Invest
, vol.73
, pp. 857-867
-
-
Rebouche, CJ1
Engel, AG2
-
21
-
-
0030712175
-
Sudden neonatal death in carnitine transporter deficiency
-
Rinaldo P Stanley CA Hsu BYL Sudden neonatal death in carnitine transporter deficiency J Pediatr 131 1997 304 305
-
(1997)
J Pediatr
, vol.131
, pp. 304-305
-
-
Rinaldo, P1
Stanley, CA2
Hsu, BYL3
-
22
-
-
0024313361
-
Carnitine status of lacto-ovovegetarians and strict vegetarian adults and children
-
Lombard KA Olson AL Nelson SE Carnitine status of lacto-ovovegetarians and strict vegetarian adults and children Am J Clin Nutr 50 1989 301 306
-
(1989)
Am J Clin Nutr
, vol.50
, pp. 301-306
-
-
Lombard, KA1
Olson, AL2
Nelson, SE3
-
23
-
-
0029090038
-
Diagnosis of inborn errors of metabolism in sudden death cases by acylcarnitine analysis of postmortem bile
-
Rashed MS Ozand PT Bennet MJ Diagnosis of inborn errors of metabolism in sudden death cases by acylcarnitine analysis of postmortem bile Clin Chem 41 1995 1109 1114
-
(1995)
Clin Chem
, vol.41
, pp. 1109-1114
-
-
Rashed, MS1
Ozand, PT2
Bennet, MJ3
-
24
-
-
0031042750
-
Bacterial carnitine metabolism
-
Kleber H-P Bacterial carnitine metabolism FEMS Microbiol Let 147 1997 1 9
-
(1997)
FEMS Microbiol Let
, vol.147
, pp. 1-9
-
-
Kleber, H-P1
-
26
-
-
0032195325
-
Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency
-
Scaglia F Wang Y Singh RH Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency Genetics in Medicine 1 1998 34 39
-
(1998)
Genetics in Medicine
, vol.1
, pp. 34-39
-
-
Scaglia, F1
Wang, Y2
Singh, RH3
-
27
-
-
0029558008
-
Renal handling of carnitine in ill preterm and term neonates
-
Zamora S Benador N Lacourt G Renal handling of carnitine in ill preterm and term neonates J Pediatr 127 1995 975 978
-
(1995)
J Pediatr
, vol.127
, pp. 975-978
-
-
Zamora, S1
Benador, N2
Lacourt, G3
-
28
-
-
0018692744
-
Plasma carnitine levels during intravenous feeding of the neonate
-
Schiff D Chan G Seccombe D Plasma carnitine levels during intravenous feeding of the neonate J Pediatr 95 1979 1043 1046
-
(1979)
J Pediatr
, vol.95
, pp. 1043-1046
-
-
Schiff, D1
Chan, G2
Seccombe, D3
-
29
-
-
0020067077
-
Carnitine blood concentrations and fat utilization in parenterally alimented premature newborn infants
-
Schmidt-Sommerfeld E Penn D Wolf H Carnitine blood concentrations and fat utilization in parenterally alimented premature newborn infants J Pediatr 100 1982 260 264
-
(1982)
J Pediatr
, vol.100
, pp. 260-264
-
-
Schmidt-Sommerfeld, E1
Penn, D2
Wolf, H3
-
30
-
-
0000576457
-
Mitochondrial fatty acid oxidation disorders
-
Roe CR Coates PM Mitochondrial fatty acid oxidation disorders Scriver CR Beaudet AL Sly WS The Metabolic and Molecular Basis of Inherited Disease 1995 Mc Graw II New York, NY 1501 1533
-
(1995)
, pp. 1501-1533
-
-
Roe, CR1
Coates, PM2
-
31
-
-
0032493741
-
Molecular and functional identification of sodium-ion dependent, high affinity human carnitine transporter OCTN2
-
Tamai I Ohashi R Nezu J Molecular and functional identification of sodium-ion dependent, high affinity human carnitine transporter OCTN2 J Biol Chem 273 1998 20378 20382
-
(1998)
J Biol Chem
, vol.273
, pp. 20378-20382
-
-
Tamai, I1
Ohashi, R2
Nezu, J3
-
32
-
-
0032231462
-
Evidence for linkage of human primary carnitine deficiency with D5S436: A novel gene locus on chromosome 5q
-
Shoji Y Koizumi A Kayo T Evidence for linkage of human primary carnitine deficiency with D5S436: A novel gene locus on chromosome 5q Am J Hum Genet 63 1998 101 108
-
(1998)
Am J Hum Genet
, vol.63
, pp. 101-108
-
-
Shoji, Y1
Koizumi, A2
Kayo, T3
-
33
-
-
0032953645
-
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium-ion dependent carnitine transporter
-
Nezu J Tamai I Oku A Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium-ion dependent carnitine transporter Nat Genet 21 1999 91 94
-
(1999)
Nat Genet
, vol.21
, pp. 91-94
-
-
Nezu, J1
Tamai, I2
Oku, A3
-
34
-
-
0033515017
-
Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency
-
Wang Y Ye J Ganapathy V Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency Proc Natl Acad Sci U S A 96 1999 2356 2360
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2356-2360
-
-
Wang, Y1
Ye, J2
Ganapathy, V3
-
35
-
-
0031568912
-
Fine chromosome mapping of the genes for human liver and muscle carnitine palmitoyltransferase I (CPT1A and CPT1B)
-
Britton CH Mackey DW Esser V Fine chromosome mapping of the genes for human liver and muscle carnitine palmitoyltransferase I (CPT1A and CPT1B) Genomics 40 1997 209 211
-
(1997)
Genomics
, vol.40
, pp. 209-211
-
-
Britton, CH1
Mackey, DW2
Esser, V3
-
36
-
-
0032145885
-
Molecular basis of hepatic carnitine palmitoyl transferase 1 deficiency
-
Ijist L Mandel H Oostheim W Molecular basis of hepatic carnitine palmitoyl transferase 1 deficiency J Clin Invest 102 1998 527 531
-
(1998)
J Clin Invest
, vol.102
, pp. 527-531
-
-
Ijist, L1
Mandel, H2
Oostheim, W3
-
37
-
-
0031424187
-
Assignment of the carnitine/acylcarnitine translocase gene (CACT) to human chromosome band 3p21.31 by in situ hybridization
-
Viggiano L Iacobazzi V Marzella R Assignment of the carnitine/acylcarnitine translocase gene (CACT) to human chromosome band 3p21.31 by in situ hybridization Cytogenet Cell Genet 79 1997 62 63
-
(1997)
Cytogenet Cell Genet
, vol.79
, pp. 62-63
-
-
Viggiano, L1
Iacobazzi, V2
Marzella, R3
-
38
-
-
17344366560
-
Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient
-
Huizing M Iacobazzi V IJlst L Cloning of the human carnitine-acylcarnitine carrier cDNA and identification of the molecular defect in a patient Am J Hum Genet 61 1997 1239 1245
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1239-1245
-
-
Huizing, M1
Iacobazzi, V2
IJlst, L3
-
39
-
-
0028007110
-
Assigment of the human carnitine palmitoyltransferase II gene (CTP1) to chromosome 1p32
-
Gellera C Verderio E Floridia G Assigment of the human carnitine palmitoyltransferase II gene (CTP1) to chromosome 1p32 Genomics 24 1994 195 197
-
(1994)
Genomics
, vol.24
, pp. 195-197
-
-
Gellera, C1
Verderio, E2
Floridia, G3
-
40
-
-
0027302901
-
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
-
Taroni F Verderio E Dworzak F Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients Nat Genet 4 1993 314 320
-
(1993)
Nat Genet
, vol.4
, pp. 314-320
-
-
Taroni, F1
Verderio, E2
Dworzak, F3
-
41
-
-
0029865178
-
Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression
-
Bonnefont J-P Taroni F Cavadini P Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression Am J Hum Genet 58 1996 971 978
-
(1996)
Am J Hum Genet
, vol.58
, pp. 971-978
-
-
Bonnefont, J-P1
Taroni, F2
Cavadini, P3
-
42
-
-
0029363858
-
Familial infantile apnea and immature beta oxidation
-
Iafolla AK Browning IB Roe CR Familial infantile apnea and immature beta oxidation Pediatr Pulmonol 20 1995 167 171
-
(1995)
Pediatr Pulmonol
, vol.20
, pp. 167-171
-
-
Iafolla, AK1
Browning, IB2
Roe, CR3
-
43
-
-
0024520790
-
Congenital complete heart block in an infant with free plasma carnitine deficiency
-
Erasmus MJ Duncan WJ Tyrrell MJ Congenital complete heart block in an infant with free plasma carnitine deficiency Can J Cardiol 5 1989 47 50
-
(1989)
Can J Cardiol
, vol.5
, pp. 47-50
-
-
Erasmus, MJ1
Duncan, WJ2
Tyrrell, MJ3
-
44
-
-
0023255772
-
Plasma carnitine deficiency. Clinical observations in 51 pediatric patients
-
Winter SC Szabo-Aczel S Curry CJ Plasma carnitine deficiency. Clinical observations in 51 pediatric patients Am J Dis Child 141 1987 660 665
-
(1987)
Am J Dis Child
, vol.141
, pp. 660-665
-
-
Winter, SC1
Szabo-Aczel, S2
Curry, CJ3
-
45
-
-
0028878124
-
Effects of parenteral l-carnitine supplementation on fat metabolism and nutrition in premature infants
-
Bonner C DeBrie K Hug G Effects of parenteral l -carnitine supplementation on fat metabolism and nutrition in premature infants J Pediatr 126 1995 287 292
-
(1995)
J Pediatr
, vol.126
, pp. 287-292
-
-
Bonner, C1
DeBrie, K2
Hug, G3
-
46
-
-
0025185037
-
Effect of intravenous l-carnitine on growth parameters and fat metabolism during parenteral nutrition in the neonate
-
Helms R Mauer EC Hay WW Effect of intravenous l -carnitine on growth parameters and fat metabolism during parenteral nutrition in the neonate J Parent Enteral Nutr 14 1990 448 453
-
(1990)
J Parent Enteral Nutr
, vol.14
, pp. 448-453
-
-
Helms, R1
Mauer, EC2
Hay, WW3
-
47
-
-
0023092066
-
Effects of oral l-carnitine supplementation in low-birth-weight premature infants maintained on human milk
-
Melegh B Keener J Sander A Effects of oral l -carnitine supplementation in low-birth-weight premature infants maintained on human milk Biol Neonate 51 1987 185 193
-
(1987)
Biol Neonate
, vol.51
, pp. 185-193
-
-
Melegh, B1
Keener, J2
Sander, A3
-
48
-
-
0025186743
-
A case of carbamoyl phosphate synthetase-1 deficiency associated with secondary carnitine deficiency-L-carnitine treatment of CPS-1 deficiency
-
Mori T Tsuchiyama A Nagai K A case of carbamoyl phosphate synthetase-1 deficiency associated with secondary carnitine deficiency-L-carnitine treatment of CPS-1 deficiency Eur J Pediatr 149 1990 272 274
-
(1990)
Eur J Pediatr
, vol.149
, pp. 272-274
-
-
Mori, T1
Tsuchiyama, A2
Nagai, K3
-
49
-
-
0032063035
-
Valproate therapy does not deplete carnitine levels in otherwise healthy children
-
Hirose S Mitsudome A Yasumoto S Valproate therapy does not deplete carnitine levels in otherwise healthy children Pediatrics 101 1998 E9
-
(1998)
Pediatrics
, vol.101
, pp. E9
-
-
Hirose, S1
Mitsudome, A2
Yasumoto, S3
-
50
-
-
85119817435
-
-
Acosta PB Yannicell S ed 3 Nutrition Support Protocols 1997 Ross Metabolic Formula System Columbus, OH 1 464
-
(1997)
, pp. 1-464
-
-
Acosta, PB1
Yannicell, S2
|