-
1
-
-
0025354387
-
Food and nutrient intake of 6-12-month-old infants fed formula or cow milk: A summary of four national surveys
-
Ernst JA, Brady MS, Rickard KA. Food and nutrient intake of 6-12-month-old infants fed formula or cow milk: a summary of four national surveys. J Pediatr. 1990;117:S86-S100.
-
(1990)
J Pediatr
, vol.117
-
-
Ernst, J.A.1
Brady, M.S.2
Rickard, K.A.3
-
2
-
-
0029565892
-
The tracking of nutrient intake in young children: The Framingham children's study
-
Singer MR, Moore LL, Garrahie EJ, et al. The tracking of nutrient intake in young children: the Framingham children's study. Am J Public Health, 1995; 85:1673-1677.
-
(1995)
Am J Public Health
, vol.85
, pp. 1673-1677
-
-
Singer, M.R.1
Moore, L.L.2
Garrahie, E.J.3
-
3
-
-
0032518360
-
Roles of neuroactive amino acids in ammonia neurotoxicity
-
Albrecht J. Roles of neuroactive amino acids in ammonia neurotoxicity. J Neurosci Res. 1998;51:133-138.
-
(1998)
J Neurosci Res
, vol.51
, pp. 133-138
-
-
Albrecht, J.1
-
4
-
-
0031719230
-
Neurotoxicity of ammonia and glutamate: Molecular mechanisms and prevention
-
Felipo V, Hermenegildo C, Montoliu C, et al. Neurotoxicity of ammonia and glutamate: molecular mechanisms and prevention. Neurotoxicology. 1998;19:675-681.
-
(1998)
Neurotoxicology
, vol.19
, pp. 675-681
-
-
Felipo, V.1
Hermenegildo, C.2
Montoliu, C.3
-
5
-
-
0032427875
-
Astroglial dysfunction in hepatic encephalopathy
-
Norenberg MD. Astroglial dysfunction in hepatic encephalopathy. Metab Brain Dis. 1998;13:319-335.
-
(1998)
Metab Brain Dis
, vol.13
, pp. 319-335
-
-
Norenberg, M.D.1
-
6
-
-
0035181229
-
Role of glutamine in cerebral nitrogen metabolism and ammonia neurotoxicity
-
Cooper AJ. Role of glutamine in cerebral nitrogen metabolism and ammonia neurotoxicity. Ment Retard Dev Disabil Res Rev. 2001;7:280-286.
-
(2001)
Ment Retard Dev Disabil Res Rev
, vol.7
, pp. 280-286
-
-
Cooper, A.J.1
-
8
-
-
0022728622
-
Partial carbamyl phosphate synthetase deficiency, simulating Reye's syndrome, in a 9-year-old girl
-
Granot E, Matoth I, Lotan, C, et al. Partial carbamyl phosphate synthetase deficiency, simulating Reye's syndrome, in a 9-year-old girl. Isr J Med Sci. 1986;22:463-465.
-
(1986)
Isr J Med Sci
, vol.22
, pp. 463-465
-
-
Granot, E.1
Matoth, I.2
Lotan, C.3
-
9
-
-
0023709248
-
Late-onset ornithine carbamoyl transferase deficiency in males
-
Drogari E, Leonard JV. Late-onset ornithine carbamoyl transferase deficiency in males. Arch Dis Child. 1986; 63:1363-1367.
-
(1986)
Arch Dis Child
, vol.63
, pp. 1363-1367
-
-
Drogari, E.1
Leonard, J.V.2
-
10
-
-
0025633857
-
Late-onset orntihine transcarbamylase deficiency in male patients
-
Finkelstein JE, Hauser ER, Leonard CO, et al. Late-onset orntihine transcarbamylase deficiency in male patients. J Pediatr. 1990;117:897-902.
-
(1990)
J Pediatr
, vol.117
, pp. 897-902
-
-
Finkelstein, J.E.1
Hauser, E.R.2
Leonard, C.O.3
-
11
-
-
0025665174
-
Molecular analysis of human argininosuccinate lyase: Mutant characterization and alternative splicing of the coding region
-
Walker DC, McCloskey DA, Simard LR, et al. Molecular analysis of human argininosuccinate lyase: mutant characterization and alternative splicing of the coding region. Proc Nat Acad Sci USA. 1990;87:9625-9629.
-
(1990)
Proc Nat Acad Sci USA
, vol.87
, pp. 9625-9629
-
-
Walker, D.C.1
McCloskey, D.A.2
Simard, L.R.3
-
12
-
-
0025557890
-
Late diagnosis of congenital argininemia during administration of sodium valproate
-
Christmann D, Hirsch E, Mutschler V, et al. Late diagnosis of congenital argininemia during administration of sodium valproate. Rev Neurol (Paris). 1990;146:764-766.
-
(1990)
Rev Neurol (Paris)
, vol.146
, pp. 764-766
-
-
Christmann, D.1
Hirsch, E.2
Mutschler, V.3
-
13
-
-
0025088059
-
A new case of argininemia without spastic diplegia in a Portugese male
-
Vilarinho L, Senra V, Vilarinho A, et al. A new case of argininemia without spastic diplegia in a Portugese male. J Inherit Metab Dis. 1990;13:751-752.
-
(1990)
J Inherit Metab Dis
, vol.13
, pp. 751-752
-
-
Vilarinho, L.1
Senra, V.2
Vilarinho, A.3
-
14
-
-
0026806468
-
Carbamyl phosphate synthetase-1 deficiency discovered after valproic acid-induced coma
-
Verbiest HB, Straver JS, Colombo JP, et al. Carbamyl phosphate synthetase-1 deficiency discovered after valproic acid-induced coma. Acta Neurol Scand, 1992;86:275-279.
-
(1992)
Acta Neurol Scand
, vol.86
, pp. 275-279
-
-
Verbiest, H.B.1
Straver, J.S.2
Colombo, J.P.3
-
15
-
-
17744397286
-
Identification of two novel mutations in the SLCC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia
-
Yasuda T, Yamaguchi N, Kobayashi K, et al. Identification of two novel mutations in the SLCC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia. Hum Genet. 2000; 107:537-545.
-
(2000)
Hum Genet
, vol.107
, pp. 537-545
-
-
Yasuda, T.1
Yamaguchi, N.2
Kobayashi, K.3
-
16
-
-
0030039992
-
Relative frequency of mutations causing ornithine transcarbamylase deficiency in 78 families
-
Tuchman M, Plante RJ, Garcia-Perez MA, et al. Relative frequency of mutations causing ornithine transcarbamylase deficiency in 78 families. Hum Genet. 1996;97:274-276.
-
(1996)
Hum Genet
, vol.97
, pp. 274-276
-
-
Tuchman, M.1
Plante, R.J.2
Garcia-Perez, M.A.3
-
17
-
-
0036164461
-
Mutations and polymorphisms in the human ornithine transcarbamylase gene
-
Tuchman M, Jaleel N, Morizono H, et al. Mutations and polymorphisms in the human ornithine transcarbamylase gene. Hum Mutat. 2002;19:93-107.
-
(2002)
Hum Mutat
, vol.19
, pp. 93-107
-
-
Tuchman, M.1
Jaleel, N.2
Morizono, H.3
-
18
-
-
0022652866
-
Natural history of symptomatic partial ornithine transcarbamylase deficiency
-
Rowe PC, Newman SL, Brusilow SW. Natural history of symptomatic partial ornithine transcarbamylase deficiency. N Engl J Med. 1986;314:541-547.
-
(1986)
N Engl J Med
, vol.314
, pp. 541-547
-
-
Rowe, P.C.1
Newman, S.L.2
Brusilow, S.W.3
-
19
-
-
0023183473
-
Ornithine transcarbamylase deficiency: Adult onset of severe symptoms
-
Gilchrist JM, Coleman RA. Ornithine transcarbamylase deficiency: adult onset of severe symptoms. Ann Intern Med. 1987;106:556-558.
-
(1987)
Ann Intern Med
, vol.106
, pp. 556-558
-
-
Gilchrist, J.M.1
Coleman, R.A.2
-
20
-
-
0025296601
-
Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma
-
Arn PH, Hauser ER, Thomas GH, et al. Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma. N Engl J Med. 1990; 322:1652-1655.
-
(1990)
N Engl J Med
, vol.322
, pp. 1652-1655
-
-
Arn, P.H.1
Hauser, E.R.2
Thomas, G.H.3
-
21
-
-
0026723977
-
Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapy
-
Honeycutt D, Callahan K, Rutledge L, et al. Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapy. Neurology. 1992;42:666-668.
-
(1992)
Neurology
, vol.42
, pp. 666-668
-
-
Honeycutt, D.1
Callahan, K.2
Rutledge, L.3
-
22
-
-
0028158840
-
Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency
-
Wong J-L, Craigen WJ, O'Brien WE, et al. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency. Ann Intern Med. 1994; 120:216-217.
-
(1994)
Ann Intern Med
, vol.120
, pp. 216-217
-
-
Wong, J.-L.1
Craigen, W.J.2
O'Brien, W.E.3
-
23
-
-
0018595957
-
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic academia
-
Coude FX, Sweetman L, Nyhan WL. Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic academia. J Clin Invest. 1979;64:1544-1551.
-
(1979)
J Clin Invest
, vol.64
, pp. 1544-1551
-
-
Coude, F.X.1
Sweetman, L.2
Nyhan, W.L.3
-
24
-
-
0017897578
-
Correlation between serum propionate and blood ammonia concentrations in propionic academia
-
Wolf B, Hsia YE, Tanaka K, et al. Correlation between serum propionate and blood ammonia concentrations in propionic academia. J Pediatr. 1978; 93:471-473.
-
(1978)
J Pediatr
, vol.93
, pp. 471-473
-
-
Wolf, B.1
Hsia, Y.E.2
Tanaka, K.3
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