scholarly journals Polymorphisms in urea cycle enzyme genes are associated with persistent pulmonary hypertension of the newborn

2017 ◽  
Vol 83 (1) ◽  
pp. 142-147 ◽  
Author(s):  
Dinushan C Kaluarachchi ◽  
Caitlin J Smith ◽  
Jonathan M Klein ◽  
Jeffrey C Murray ◽  
John M Dagle ◽  
...  
Author(s):  
Dinushan Kaluarachchi ◽  
Jessica C. Smith ◽  
Bruce Bedell ◽  
Jonathan Klein ◽  
John Dagle ◽  
...  

PEDIATRICS ◽  
2016 ◽  
Vol 137 (Supplement 3) ◽  
pp. 486A-486A
Author(s):  
Dinushan Kaluarachchi ◽  
Jessica C. Smith ◽  
Bruce Bedell ◽  
Jonathan Klein ◽  
John Dagle ◽  
...  

Author(s):  
R.G. Lobetti ◽  
D.B. Miller ◽  
T. Dippenaar

A 3-year-old male German shepherd dog was presented with severe generalised seizures. The dog was protein-intolerant and showed severe hyperammonaemia on ammonia stimulation. The hyperammonaemic state was present for at least 6 weeks and then spontaneously resolved. No obvious cause (liver disease, portocaval shunts, urea cycle enzyme deficiencies, drug therapy or urinary tract obstruction) could be identified. It is possible that this dog had a variation of transient hyperammonaemic syndrome, described in man and recently in a juvenile Irish wolfhound, that extended into adulthood.


2005 ◽  
Vol 86 (4) ◽  
pp. 448-455 ◽  
Author(s):  
Phyllis B. Acosta ◽  
Steven Yannicelli ◽  
Alan S. Ryan ◽  
Georgianne Arnold ◽  
Barbara J. Marriage ◽  
...  

FEBS Letters ◽  
1996 ◽  
Vol 399 (3) ◽  
pp. 310-312 ◽  
Author(s):  
Mineko Tomomura ◽  
Akito Tomomura ◽  
Dewan Md. Abdullah Abu Musa ◽  
Takeyori Saheki

2004 ◽  
Vol 134 (10) ◽  
pp. 2775S-2782S ◽  
Author(s):  
Fernando Scaglia ◽  
Nicola Brunetti-Pierri ◽  
Soledad Kleppe ◽  
Juan Marini ◽  
Susan Carter ◽  
...  

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