نتایج جستجو برای: urea cycle disorders

تعداد نتایج: 967162  

2015
Sanzidur Rahman

Background and statement of the problem: 120 words Research methodology and data: 120 words Research findings: 120 words Policy implications 40 words. Rice is the most dominant field crop in Bangladesh covering 75% of the total cultivated area and consumes 80% of the total fertilizers alone. Nevertheless, the productivity of rice in Bangladesh remains one of the lowest in the world. Urea, the m...

2017

?Ur readers to form an opinion as o involved. They are not inconsiderab, Urea-Stibamine" has now a ;vell"^Stfnd the reputation in the treatment of kala-az , question of its supply and cost affects t ^ health Departments of four provinc caseApparently there were two issues i ^reahe first was as to the use of the na t^efamine the second the al|e|ad packed Ln,on Drug Co. was issuing the ciruj, f ^...

Journal: :European Journal of Biochemistry 2003

Journal: :Pediatric Research 1974

Journal: :Bifidobacteria and Microflora 1987

2016
Jayasimman Rajendran Nikica Tomašić Heike Kotarsky Eva Hansson Vidya Velagapudi Jukka Kallijärvi Vineta Fellman

Mitochondrial disorders cause energy failure and metabolic derangements. Metabolome profiling in patients and animal models may identify affected metabolic pathways and reveal new biomarkers of disease progression. Using liver metabolomics we have shown a starvation-like condition in a knock-in (Bcs1lc.232A>G) mouse model of GRACILE syndrome, a neonatal lethal respiratory chain complex III dysf...

Journal: :Seminars in neonatology : SN 1990
J M Saudubray C Narcy L Lyonnet J P Bonnefont B T Poll The A Munnich

Most inborn errors of intermediary metabolism presenting in the neonatal period fall schematically into three clinical categories: (1) those which lead to a neurological distress 'intoxication type' with a symptom-free interval, vomiting, comas, hypertonia, abnormal movements and frequent humoral disturbances (organic acidaemias, congenital urea cycle defects); (2) those which lead to a neurolo...

Journal: :Clinical chemistry 2003
Youri E C Taes Norbert H Lameire Marc L De Buyzere Amir Shoja Guy De Backer Joris R Delanghe

References 1. Brusilow SW, Maestri NE. Urea cycle disorders: diagnosis, pathophysiology, and therapy. Adv Pediatr 1996;43:127–70. 2. Batshaw ML, Robinson MB, Ye X, Pabin C, Daikhin Y, Burton BK, et al. Correction of ureagenesis after gene transfer in an animal model and after liver transplantation in humans with ornithine transcarbamylase deficiency. Pediatr Res 1999;46:588–93. 3. Batshaw ML, B...

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