Chalmers RA - Search Results

1

Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.

Kölker S, Hoffmann GF, Schor DS, Feyh P, Wagner L, Jeffrey I, Pourfarzam M, Okun JG, Zschocke J, Baric I, Bain MD, Jakobs C, Chalmers RA. Kölker S, et al. Among authors: chalmers ra. Neuropediatrics. 2003 Jun;34(5):253-60. doi: 10.1055/s-2003-43261. Neuropediatrics. 2003. PMID: 14598231

2

Riboflavin-responsive glutaryl CoA dehydrogenase deficiency.

Chalmers RA, Bain MD, Zschocke J. Chalmers RA, et al. Mol Genet Metab. 2006 May;88(1):29-37. doi: 10.1016/j.ymgme.2005.11.007. Mol Genet Metab. 2006. PMID: 16377226

3

Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.

Kölker S, Garbade SF, Greenberg CR, Leonard JV, Saudubray JM, Ribes A, Kalkanoglu HS, Lund AM, Merinero B, Wajner M, Troncoso M, Williams M, Walter JH, Campistol J, Martí-Herrero M, Caswill M, Burlina AB, Lagler F, Maier EM, Schwahn B, Tokatli A, Dursun A, Coskun T, Chalmers RA, Koeller DM, Zschocke J, Christensen E, Burgard P, Hoffmann GF. Kölker S, et al. Among authors: chalmers ra. Pediatr Res. 2006 Jun;59(6):840-7. doi: 10.1203/01.pdr.0000219387.79887.86. Epub 2006 Apr 26. Pediatr Res. 2006. PMID: 16641220

4

Diagnosis and management of trimethylaminuria (FMO3 deficiency) in children.

Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA. Chalmers RA, et al. J Inherit Metab Dis. 2006 Feb;29(1):162-72. doi: 10.1007/s10545-006-0158-6. J Inherit Metab Dis. 2006. PMID: 16601883 Clinical Trial.

5

Hair loss in children.

Chalmers RA, Bain MD. Chalmers RA, et al. Arch Dis Child. 1993 Sep;69(3):407-8. doi: 10.1136/adc.69.3.407-a. Arch Dis Child. 1993. PMID: 8215559 Free PMC article. No abstract available.

6

Oral cobalamin therapy.

Chalmers RA, Bain MD, Costello I. Chalmers RA, et al. Lancet. 2000 Jan 8;355(9198):148. doi: 10.1016/s0140-6736(05)72065-1. Lancet. 2000. PMID: 10675197 No abstract available.

7

Dietary restriction and methylmalonicaciduria.

Bain MD, Chalmers RA, Stacey TE. Bain MD, et al. Among authors: chalmers ra. Lancet. 1989 Aug 5;2(8658):337. doi: 10.1016/s0140-6736(89)90526-6. Lancet. 1989. PMID: 2569141 No abstract available.

8

Use of human somatotrophin in the treatment of a patient with methylmalonic aciduria.

Bain MD, Nussey SS, Jones M, Chalmers RA. Bain MD, et al. Among authors: chalmers ra. Eur J Pediatr. 1995 Oct;154(10):850-2. doi: 10.1007/BF01959796. Eur J Pediatr. 1995. PMID: 8529687

9

The entrapment of mannose-terminated glucocerebrosidase (Alglucerase) in human carrier erythrocytes.

Bax BE, Bain MD, Ward CP, Fensom AH, Chalmers RA. Bax BE, et al. Among authors: chalmers ra. Biochem Soc Trans. 1996 Aug;24(3):441S. doi: 10.1042/bst024441s. Biochem Soc Trans. 1996. PMID: 8878985 No abstract available.

10

The entrapment of polyethylene glycol-bound adenosine deaminase (Pegademase) in human carrier erythrocytes.

Bax BE, Fairbanks LD, Bain MD, Simmonds HA, Chalmers RA. Bax BE, et al. Among authors: chalmers ra. Biochem Soc Trans. 1996 Aug;24(3):442S. doi: 10.1042/bst024442s. Biochem Soc Trans. 1996. PMID: 8878986 No abstract available.

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