294 related articles for article (PubMed ID: 29356227)
1. Efficacy of peritoneal dialysis in neonates presenting with hyperammonaemia due to urea cycle defects and organic acidaemia.
Celik M; Akdeniz O; Ozgun N
Nephrology (Carlton); 2019 Mar; 24(3):330-335. PubMed ID: 29356227
[TBL] [Abstract][Full Text] [Related]
2. Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism.
Arbeiter AK; Kranz B; Wingen AM; Bonzel KE; Dohna-Schwake C; Hanssler L; Neudorf U; Hoyer PF; Büscher R
Nephrol Dial Transplant; 2010 Apr; 25(4):1257-65. PubMed ID: 19934086
[TBL] [Abstract][Full Text] [Related]
3. Peritoneal dialysis in neonates with inborn errors of metabolism: is it really out of date?
Pela I; Seracini D; Donati MA; Lavoratti G; Pasquini E; Materassi M
Pediatr Nephrol; 2008 Jan; 23(1):163-8. PubMed ID: 17899205
[TBL] [Abstract][Full Text] [Related]
4. Short-term results of continuous venovenous haemodiafiltration versus peritoneal dialysis in 40 neonates with inborn errors of metabolism.
Celik M; Akdeniz O; Ozgun N; Ipek MS; Ozbek MN
Eur J Pediatr; 2019 Jun; 178(6):829-836. PubMed ID: 30895385
[TBL] [Abstract][Full Text] [Related]
5. Treatment of a neonate with propionic acidaemia and severe hyperammonaemia by peritoneal dialysis.
Robert MF; Schultz DJ; Wolf B; Cochran WD; Schwartz AL
Arch Dis Child; 1979 Dec; 54(12):962-5. PubMed ID: 533302
[TBL] [Abstract][Full Text] [Related]
6. Peritoneal dialysis in the treatment of metabolic crises caused by inherited disorders of organic and amino acid metabolism.
Gortner L; Leupold D; Pohlandt F; Bartmann P
Acta Paediatr Scand; 1989 Sep; 78(5):706-11. PubMed ID: 2596277
[TBL] [Abstract][Full Text] [Related]
7. Differential response to renal replacement therapy in neonatal-onset inborn errors of metabolism.
Porta F; Peruzzi L; Bonaudo R; Pieretti S; Busso M; Cocchi E; Conio A; Pagliardini V; Spada M
Nephrology (Carlton); 2018 Oct; 23(10):957-961. PubMed ID: 29888426
[TBL] [Abstract][Full Text] [Related]
8. The utility of EEG monitoring in neonates with hyperammonemia due to inborn errors of metabolism.
Wiwattanadittakul N; Prust M; Gaillard WD; Massaro A; Vezina G; Tsuchida TN; Gropman AL
Mol Genet Metab; 2018 Nov; 125(3):235-240. PubMed ID: 30197275
[TBL] [Abstract][Full Text] [Related]
9. Dialysis in neonates with inborn errors of metabolism.
Schaefer F; Straube E; Oh J; Mehls O; Mayatepek E
Nephrol Dial Transplant; 1999 Apr; 14(4):910-8. PubMed ID: 10328469
[TBL] [Abstract][Full Text] [Related]
10. Primary hyperammonaemia: Current diagnostic and therapeutic strategies.
Häberle J
J Mother Child; 2020 Oct; 24(2):32-38. PubMed ID: 33179600
[TBL] [Abstract][Full Text] [Related]
11. Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study.
Valayannopoulos V; Baruteau J; Delgado MB; Cano A; Couce ML; Del Toro M; Donati MA; Garcia-Cazorla A; Gil-Ortega D; Gomez-de Quero P; Guffon N; Hofstede FC; Kalkan-Ucar S; Coker M; Lama-More R; Martinez-Pardo Casanova M; Molina A; Pichard S; Papadia F; Rosello P; Plisson C; Le Mouhaer J; Chakrapani A
Orphanet J Rare Dis; 2016 Mar; 11():32. PubMed ID: 27030250
[TBL] [Abstract][Full Text] [Related]
12. Inborn Errors of Metabolism with Hyperammonemia: Urea Cycle Defects and Related Disorders.
Summar ML; Mew NA
Pediatr Clin North Am; 2018 Apr; 65(2):231-246. PubMed ID: 29502911
[TBL] [Abstract][Full Text] [Related]
13. Neonatal factors related to survival and intellectual and developmental outcome of patients with early-onset urea cycle disorders.
Pontoizeau C; Roda C; Arnoux JB; Vignolo-Diard P; Brassier A; Habarou F; Barbier V; Grisel C; Abi-Warde MT; Boddaert N; Kuster A; Servais A; Kaminska A; Hennequin C; Dupic L; Lesage F; Touati G; Valayannopoulos V; Chadefaux-Vekemans B; Oualha M; Eisermann M; Ottolenghi C; de Lonlay P
Mol Genet Metab; 2020 Jun; 130(2):110-117. PubMed ID: 32273051
[TBL] [Abstract][Full Text] [Related]
14. Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.
Enns GM; Berry SA; Berry GT; Rhead WJ; Brusilow SW; Hamosh A
N Engl J Med; 2007 May; 356(22):2282-92. PubMed ID: 17538087
[TBL] [Abstract][Full Text] [Related]
15. A retrospective study of adult patients with noncirrhotic hyperammonemia.
Stergachis AB; Mogensen KM; Khoury CC; Lin AP; Peake RW; Baker JJ; Barkoudah E; Sahai I; Sweetser DA; Berry GT; Krier JB
J Inherit Metab Dis; 2020 Nov; 43(6):1165-1172. PubMed ID: 32713002
[TBL] [Abstract][Full Text] [Related]
16. N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia.
Jones S; Reed CA; Vijay S; Walter JH; Morris AA
J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S219-22. PubMed ID: 18338235
[TBL] [Abstract][Full Text] [Related]
17. [Neonatal hyperammonemia].
Jaeken J; Devlieger H; Evens M; Casaer P; Eggermont E
Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
[TBL] [Abstract][Full Text] [Related]
18. Treatment of hyperammonemic coma caused by inborn errors of urea synthesis.
Batshaw ML; Brusilow SW
J Pediatr; 1980 Dec; 97(6):893-900. PubMed ID: 7441417
[TBL] [Abstract][Full Text] [Related]
19. Utility of peritoneal dialysis in neonates affected by inborn errors of metabolism.
Bilgin L; Unal S; Gunduz M; Uncu N; Tiryaki T
J Paediatr Child Health; 2014 Jul; 50(7):531-5. PubMed ID: 24612162
[TBL] [Abstract][Full Text] [Related]
20. Severe hyperammonaemia in adults not explained by liver disease.
Walker V
Ann Clin Biochem; 2012 May; 49(Pt 3):214-28. PubMed ID: 22349554
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]