Hendriksz C - Search Results

1

McClelland VM, Gissen P, Hendriksz C, Chakrapani A. McClelland VM, et al. Among authors: hendriksz c. Pediatr Res. 2007 Jan;61(1):134; author reply 134-5. doi: 10.1203/01.pdr.0b013e31802d9ab4. Pediatr Res. 2007. PMID: 17211155 No abstract available.

2

Glutaric aciduria type 1 presenting with epilepsy.

McClelland VM, Bakalinova DB, Hendriksz C, Singh RP. McClelland VM, et al. Among authors: hendriksz c. Dev Med Child Neurol. 2009 Mar;51(3):235-9. doi: 10.1111/j.1469-8749.2008.03240.x. Dev Med Child Neurol. 2009. PMID: 19260933 Free article.

3

Case 36-2005: a woman with seizure, disturbed gait, and altered mental status.

Geberhiwot T, Chakrapani A, Hendriksz C. Geberhiwot T, et al. Among authors: hendriksz c. N Engl J Med. 2006 Mar 9;354(10):1096-7; author reply 1096-7. doi: 10.1056/NEJMc053506. N Engl J Med. 2006. PMID: 16525154 No abstract available.

4

Successful pregnancy in a treated patient with biotinidase deficiency.

Hendriksz CJ, Preece MA, Chakrapani A. Hendriksz CJ, et al. J Inherit Metab Dis. 2005;28(5):791-2. doi: 10.1007/s10545-005-0060-7. J Inherit Metab Dis. 2005. PMID: 16151912

5

Dietary practices in glutaric aciduria type 1 over 16 years.

Gokmen-Ozel H, MacDonald A, Daly A, Ashmore C, Preece MA, Hendriksz C, Vijay S, Chakrapani A. Gokmen-Ozel H, et al. Among authors: hendriksz c. J Hum Nutr Diet. 2012 Dec;25(6):514-9. doi: 10.1111/j.1365-277X.2012.01269.x. Epub 2012 Jul 30. J Hum Nutr Diet. 2012. PMID: 22845646

6

Prospective treatment in carnitine-acylcarnitine translocase deficiency.

Pierre G, Macdonald A, Gray G, Hendriksz C, Preece MA, Chakrapani A. Pierre G, et al. Among authors: hendriksz c. J Inherit Metab Dis. 2007 Oct;30(5):815. doi: 10.1007/s10545-007-0518-x. Epub 2007 May 12. J Inherit Metab Dis. 2007. PMID: 17508264

7

Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UK.

Hutchin T, Preece MA, Hendriksz C, Chakrapani A, McClelland V, Okumura F, Song YZ, Iijima M, Kobayashi K, Saheki T, McKiernan P, Baumann U. Hutchin T, et al. Among authors: hendriksz c. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S151-5. doi: 10.1007/s10545-009-1116-x. Epub 2009 Jun 11. J Inherit Metab Dis. 2009. PMID: 19517266

8

Oculomotor abnormalities in children with Niemann-Pick type C.

Blundell J, Frisson S, Chakrapani A, Gissen P, Hendriksz C, Vijay S, Olson A. Blundell J, et al. Among authors: hendriksz c. Mol Genet Metab. 2018 Feb;123(2):159-168. doi: 10.1016/j.ymgme.2017.11.004. Epub 2017 Nov 16. Mol Genet Metab. 2018. PMID: 29191430

9

Markers of cognitive function in individuals with metabolic disease: Morquio syndrome and tyrosinemia type III.

Blundell J, Frisson S, Chakrapani A, Kearney S, Vijay S, MacDonald A, Gissen P, Hendriksz C, Olson A. Blundell J, et al. Among authors: hendriksz c. Cogn Neuropsychol. 2018 May-Jun;35(3-4):120-147. doi: 10.1080/02643294.2018.1443913. Cogn Neuropsychol. 2018. PMID: 29741470

10

Bone marrow transplantation in glycogen storage disease type 1b.

Pierre G, Chakupurakal G, McKiernan P, Hendriksz C, Lawson S, Chakrapani A. Pierre G, et al. Among authors: hendriksz c. J Pediatr. 2008 Feb;152(2):286-8. doi: 10.1016/j.jpeds.2007.09.031. J Pediatr. 2008. PMID: 18206704

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