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Items: 1 to 20 of 152

1.

Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.

Scott-Emuakpor A, Higgins JV, Kohrman AF.

Pediatr Res. 1972 Jul;6(7):626-33. No abstract available.

PMID:
5057291
2.

Citrullinemia with defective urea production.

Morrow G 3rd, Barness LA, Efron ML.

Pediatrics. 1967 Oct;40(4):565-74. No abstract available.

PMID:
6051056
3.

[Citrullinemia].

Vidailhet M, Levin B, Dautrevaux M, Paysant P, Gelot S, Badonnel Y, Pierson M, Neimann N.

Arch Fr Pediatr. 1971 May;28(5):521-32. French. No abstract available.

PMID:
5561754
4.

Citrullinemia: investigation and treatment over a four-year period.

Buist NR, Kennaway NG, Hepburn CA, Strandholm JJ, Ramberg DA.

J Pediatr. 1974 Aug;85(2):208-14. No abstract available.

PMID:
4842795
5.

Familial protein intolerance. Possible nature of enzyme defect.

Malmquist J, Jagenburg R, Lindstedt G.

N Engl J Med. 1971 May 6;284(18):997-1002. No abstract available.

PMID:
5553484
6.

A case of transient neonatal citrullinemia.

Ohtake A, Takayanagi M, Ogura N, Nakajima H.

Eur J Pediatr. 1983 Oct;141(1):60-1.

PMID:
6641770
7.

Haloperidol-induced hyperammonaemia in a child with citrullinaemia.

Rubenstein JL, Johnston K, Elliott GR, Brusilow SW.

J Inherit Metab Dis. 1990;13(5):754-5. No abstract available.

PMID:
2246861
8.

Inherited hyperammonemic syndromes.

Hsia YE.

Gastroenterology. 1974 Aug;67(2):347-74. Review. No abstract available.

PMID:
4368001
9.
10.

Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport.

Fell V, Pollitt RJ, Sampson GA, Wright T.

Am J Dis Child. 1974 May;127(5):752-6. No abstract available.

PMID:
4825593
11.

Citrullinemia and an alternative urea cycle.

Levin B, Oberholzer VG, Palmer T.

Pediatr Res. 1973 Aug;7(8):728. No abstract available.

PMID:
4732112
12.

Neurological abnormalities in primary hyperammonaemia.

Hopkins IJ, Connelly JF, Hocking B, Maddison TG.

Proc Aust Assoc Neurol. 1968;5(1):183-7. No abstract available.

PMID:
5709958
13.

[Argininosuccinic aciduria with and without hyperammoniemia. Study of 2 cases].

Tancredi F, Striano S, Ragonese G, Cedrola G, Guazzi GC.

Minerva Pediatr. 1973 Mar 3;25(7):280-8. Italian. No abstract available.

PMID:
4707412
14.

Metabolic errors in lysine degradation.

Carson NA.

Clin Endocrinol Metab. 1974 Mar;3(1):71-86. Review. No abstract available.

PMID:
4609650
15.

Role of argininosuccinate synthetase in the regulation of urea synthesis in the rat and argininosuccinate synthetase-associated metabolic disorder in man.

Saheki T, Tsuda M, Takada S, Kusumi K, Katsunuma T.

Adv Enzyme Regul. 1980;18:221-38. No abstract available.

PMID:
7446299
16.

[Disorder of synthesis of ammonia and urea and excretion of amino acids in acute peritonitis].

Savchuk BD, Abramovich AB, Lemish GT.

Klin Med (Mosk). 1973 Nov;51(11):107-11. Russian. No abstract available.

PMID:
4787291
17.

Lysine intolerance in a variant form of citrullinemia.

Matsuda I, Arashima S, Imanishi Y, Yamamoto J, Akaboshi I, Shinozuka S, Nagata N.

Pediatr Res. 1979 Oct;13(10):1134-6.

PMID:
503639
18.

Citrullinemia. A preliminary case report.

Morrow G.

Am J Dis Child. 1967 Jan;113(1):157-9. No abstract available.

PMID:
6015894
19.

[Hereditary anomalies of the urea cycle].

Berger R, Broyer M.

Presse Med. 1968 May 18;76(24):1183-4. French. No abstract available.

PMID:
5673388
20.

[A case of combined lysinuric protein intolerance and hypoactivity of argininosuccinate synthetase (citrullinemia)].

Shioya K, Yamamura Y, Kurihara T, Matsukura S.

Nihon Naika Gakkai Zasshi. 1988 May;77(5):667-73. Japanese. No abstract available.

PMID:
3145960

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