Serial diffusion-weighted magnetic resonance imaging in adult-onset citrullinaemia

Author:

Au Wing Lok,Lim Tchoyoson C.C.,Seow Dennis C.C.,Koh Pei Lin,Loh Ngai Kun,Lim Maria S.F.,Tan It Koon,Yee Woon Chee

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. Online Mendelian Inheritance in Man, OMIM (TM). Johns Hopkins University, Baltimore, MD. MIM Number: #603471:4/3/2001. World Wide Web URL: http://www.ncbi.nlm.nih.gov/omim/.

2. Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinaemia;Yasuda;Hum. Genet.,2000

3. Case report: recurrent hyperammonaemic encephalopathy due to citrullinaemia in a 52 year old man;Chow;J. Gastroenterol. Hepatol.,1996

4. Adult-type citrullinaemia;Okeda;Acta Neuropathol. (Berl.),1989

5. Citrullinaemia type II in a 64-year-old man with fluctuating serum citrulline levels;Maruyama;J. Neurol. Sci.,2001

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