Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.-Reference-Cited by-同舟云学术

Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.

Published:1983-01-01 Issue:1 Volume:46 Page:28-34
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Kendall B E,Kingsley D P,Leonard J V,Lingam S,Oberholzer V G

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference20 articles.

1. Hereditary hyperammonaemic syndromes-a six year experience;Haan, E.A.; Danks, D.M.; Hoogenraad, N.J.; Rogers, J.G.;Austr Paediatr J,1979

2. The management of life-threatening hyperammonaemia: a comparison of several therapeutic. modalities;Wiegand, C.; Thompson, T.; Bock, G.H.; Mathis, R.K.; Kjellstrand, C.M.; Mauer, S.M.;J Pediatr,1980

3. Comparison of exchange transfusion, peritoneal dialysis and haemodialysis for the;Donn, S.M.; Swartz, R.D.; Thoene, J.G.;J Pediatr; OberhoL/er treatment of hyperammonaemia in an anuric new born infant,1979

4. Urea Cycle disorders and other congenital hyperammonaemic syndromes;Shih, V.E.,1978

5. Hereditary ornithine transcarbamylase deficiency;Saudubray, J.M.; Charpentier, Cathelineau L.Laugier J.M.; C, LeJeune; JA, Mozziconacci; P.;Acta PaedSclanid,1975

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