Bain M - Search Results

1

Obesity, oxidative DNA damage and vitamin D as predictors of genomic instability in children and adolescents.

Usman M, Woloshynowych M, Britto JC, Bilkevic I, Glassar B, Chapman S, Ford-Adams ME, Desai A, Bain M, Tewfik I, Volpi EV. Usman M, et al. Among authors: bain m. Int J Obes (Lond). 2021 Sep;45(9):2095-2107. doi: 10.1038/s41366-021-00879-2. Epub 2021 Jun 22. Int J Obes (Lond). 2021. PMID: 34158611 Free PMC article.

2

Haemorheology in Gaucher disease.

Bax BE, Richfield L, Bain MD, Mehta AB, Chalmers RA, Rampling MW. Bax BE, et al. Eur J Haematol. 2005 Sep;75(3):252-8. doi: 10.1111/j.1600-0609.2005.00496.x. Eur J Haematol. 2005. PMID: 16104883

3

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: bain md. Biochem Soc Trans. 1996 Aug;24(3):441S. doi: 10.1042/bst024441s. Biochem Soc Trans. 1996. PMID: 8878985 No abstract available.

4

Newborn screening for inborn errors of metabolism: a systematic review.

Seymour CA, Thomason MJ, Chalmers RA, Addison GM, Bain MD, Cockburn F, Littlejohns P, Lord J, Wilcox AH. Seymour CA, et al. Among authors: bain md. Health Technol Assess. 1997;1(11):i-iv, 1-95. Health Technol Assess. 1997. PMID: 9483156 Free article. Review.

5

Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation.

Cattoni A, Jackson C, Bain M, Houghton J, Wei C. Cattoni A, et al. Among authors: bain m. Pediatr Diabetes. 2019 Jun;20(4):482-485. doi: 10.1111/pedi.12826. Epub 2019 Apr 2. Pediatr Diabetes. 2019. PMID: 30734462

6

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: bain md. Biochem Soc Trans. 1996 Aug;24(3):442S. doi: 10.1042/bst024442s. Biochem Soc Trans. 1996. PMID: 8878986 No abstract available.

7

A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolism.

Thomason MJ, Lord J, Bain MD, Chalmers RA, Littlejohns P, Addison GM, Wilcox AH, Seymour CA. Thomason MJ, et al. Among authors: bain md. J Public Health Med. 1998 Sep;20(3):331-43. doi: 10.1093/oxfordjournals.pubmed.a024777. J Public Health Med. 1998. PMID: 9793900 Review.

8

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

Chalmers RA, Bain MD, Michelakakis H, Zschocke J, Iles RA. Chalmers RA, et al. Among authors: bain md. 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.

9

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. Eur J Pediatr. 1995 Oct;154(10):850-2. doi: 10.1007/BF01959796. Eur J Pediatr. 1995. PMID: 8529687

10

A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency.

Bax BE, Bain MD, Fairbanks LD, Webster AD, Ind PW, Hershfield MS, Chalmers RA. Bax BE, et al. Eur J Haematol. 2007 Oct;79(4):338-48. doi: 10.1111/j.1600-0609.2007.00927.x. Epub 2007 Aug 3. Eur J Haematol. 2007. PMID: 17680812

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