Mundy H - Search Results

1

Long-term use of investigational β-Hydroxybutyrate salts in children with multiple acyl-CoA dehydrogenase or pyruvate dehydrogenase deficiency.

Morris AAM, Cuenoud B, Delerive P, Mundy H, Schwahn BC. Morris AAM, et al. Among authors: mundy h. Mol Genet Metab Rep. 2024 Jun 18;40:101104. doi: 10.1016/j.ymgmr.2024.101104. eCollection 2024 Sep. Mol Genet Metab Rep. 2024. PMID: 38983107 Free PMC article.

2

Glycogenosis type I and diabetes mellitus: a common mechanism for renal dysfunction?

Mundy HR, Lee PJ. Mundy HR, et al. Med Hypotheses. 2002 Jul;59(1):110-4. doi: 10.1016/s0306-9877(02)00199-8. Med Hypotheses. 2002. PMID: 12160694

3

Reduction in bone mineral density in glycogenosis type III may be due to a mixed muscle and bone deficit.

Mundy HR, Williams JE, Lee PJ, Fewtrell MS. Mundy HR, et al. J Inherit Metab Dis. 2008 Jun;31(3):418-23. doi: 10.1007/s10545-008-0830-0. Epub 2008 Apr 4. J Inherit Metab Dis. 2008. PMID: 18392743

4

The regulation of growth in glycogen storage disease type 1.

Mundy HR, Hindmarsh PC, Matthews DR, Leonard JV, Lee PJ. Mundy HR, et al. Clin Endocrinol (Oxf). 2003 Mar;58(3):332-9. doi: 10.1046/j.1365-2265.2003.01717.x. Clin Endocrinol (Oxf). 2003. PMID: 12608939

5

Dietary control of phenylketonuria.

Mundy H, Lilburn M, Cousins A, Lee P. Mundy H, et al. Lancet. 2002 Dec 21-28;360(9350):2076. doi: 10.1016/S0140-6736(02)11959-3. Lancet. 2002. PMID: 12504429 No abstract available.

6

A randomized controlled study of modified cobratoxin in adrenomyeloneuropathy.

Mundy HR, Jones SJ, Hobart JC, Hanna MG, Lee PJ. Mundy HR, et al. Neurology. 2003 Aug 26;61(4):528-30. doi: 10.1212/01.wnl.0000079460.21925.d3. Neurology. 2003. PMID: 12939429 Clinical Trial.

7

A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy.

Alston CL, Morak M, Reid C, Hargreaves IP, Pope SA, Land JM, Heales SJ, Horvath R, Mundy H, Taylor RW. Alston CL, et al. Among authors: mundy h. Neuromuscul Disord. 2010 Feb;20(2):131-5. doi: 10.1016/j.nmd.2009.10.010. Epub 2009 Dec 16. Neuromuscul Disord. 2010. PMID: 20018511

8

Exercise capacity and biochemical profile during exercise in patients with glycogen storage disease type I.

Mundy HR, Georgiadou P, Davies LC, Cousins A, Leonard JV, Lee PJ. Mundy HR, et al. J Clin Endocrinol Metab. 2005 May;90(5):2675-80. doi: 10.1210/jc.2004-0890. Epub 2005 Jan 25. J Clin Endocrinol Metab. 2005. PMID: 15671110

9

The effect of L-alanine therapy in a patient with adult onset glycogen storage disease type II.

Mundy HR, Williams JE, Cousins AJ, Lee PJ. Mundy HR, et al. J Inherit Metab Dis. 2006 Feb;29(1):226-9. doi: 10.1007/s10545-006-0238-7. J Inherit Metab Dis. 2006. PMID: 16601900 Clinical Trial.

10

Molybdenum cofactor deficiency presenting with a parkinsonism-dystonia syndrome.

Alkufri F, Harrower T, Rahman Y, Hughes E, Mundy H, Knibb JA, Moriarty J, Connor S, Samuel M. Alkufri F, et al. Among authors: mundy h. Mov Disord. 2013 Mar;28(3):399-401. doi: 10.1002/mds.25276. Epub 2013 Feb 22. Mov Disord. 2013. PMID: 23436702 No abstract available.

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