Monavari AA - Search Results

1

Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatment.

Coss KP, Doran PP, Owoeye C, Codd MB, Hamid N, Mayne PD, Crushell E, Knerr I, Monavari AA, Treacy EP. Coss KP, et al. Among authors: monavari aa. J Inherit Metab Dis. 2013 Jan;36(1):21-7. doi: 10.1007/s10545-012-9507-9. Epub 2012 Jul 3. J Inherit Metab Dis. 2013. PMID: 22870861

2

Glutaric aciduria type I: outcome in the Republic of Ireland.

Naughten ER, Mayne PD, Monavari AA, Goodman SI, Sulaiman G, Croke DT. Naughten ER, et al. Among authors: monavari aa. J Inherit Metab Dis. 2004;27(6):917-20. doi: 10.1023/B:BOLI.0000045777.82784.74. J Inherit Metab Dis. 2004. PMID: 15505400

3

Mitochondrial cytopathies, phenotypic heterogeneity and a high incidence.

Ryan E, King MD, Rustin P, Mayne PD, Brown GK, Monavari AA, Walsh R, Treacy EP. Ryan E, et al. Among authors: monavari aa. Ir Med J. 2006 Oct;99(9):262-4. Ir Med J. 2006. PMID: 17144232

4

Long chain fatty acid oxidation defects in children: importance of detection and treatment options.

Hayes B, Lynch B, O'Keefe M, Monavari AA, Treacy EP. Hayes B, et al. Among authors: monavari aa. Ir J Med Sci. 2007 Sep;176(3):189-92. doi: 10.1007/s11845-007-0025-y. Epub 2007 Apr 13. Ir J Med Sci. 2007. PMID: 17431731

5

Outcomes of siblings with classical galactosemia.

Hughes J, Ryan S, Lambert D, Geoghegan O, Clark A, Rogers Y, Hendroff U, Monavari A, Twomey E, Treacy EP. Hughes J, et al. J Pediatr. 2009 May;154(5):721-6. doi: 10.1016/j.jpeds.2008.11.052. Epub 2009 Feb 1. J Pediatr. 2009. PMID: 19181333

6

Should children with inherited metabolic disorders receive varicella vaccination?

Varghese M, Cafferkey M, O'Regan M, Monavari AA, Treacy EP. Varghese M, et al. Among authors: monavari aa. Arch Dis Child. 2011 Jan;96(1):99-100. doi: 10.1136/adc.2008.147934. Epub 2009 Oct 21. Arch Dis Child. 2011. PMID: 19846994

7

Integrin α(IIb)β₃ exists in an activated state in subjects with elevated plasma homocysteine levels.

McGarrigle SA, O'Neill S, Walsh GM, Moran N, Graham IM, Cooney MT, Monavari A, Mayne P, Collins P. McGarrigle SA, et al. Platelets. 2011;22(1):65-73. doi: 10.3109/09537104.2010.512646. Epub 2010 Dec 6. Platelets. 2011. PMID: 21133649 Free article.

8

Parental experience of enzyme replacement therapy for Hunter syndrome.

Buraczewska M, O'Leary D, Walsh O, Monavari A, Crushell E. Buraczewska M, et al. Ir Med J. 2013 Apr;106(4):120-2. Ir Med J. 2013. PMID: 23691848

9

Clinical and genetic characterisation of infantile liver failure syndrome type 1, due to recessive mutations in LARS.

Casey JP, Slattery S, Cotter M, Monavari AA, Knerr I, Hughes J, Treacy EP, Devaney D, McDermott M, Laffan E, Wong D, Lynch SA, Bourke B, Crushell E. Casey JP, et al. Among authors: monavari aa. J Inherit Metab Dis. 2015 Nov;38(6):1085-92. doi: 10.1007/s10545-015-9849-1. Epub 2015 Apr 28. J Inherit Metab Dis. 2015. PMID: 25917789

10

'Malignant Phenylketonuria' (PKU) Due to Dihydropteridine Reductase (DHPR) Deficiency.

Ventzke A, Hoffmann J, Crushell E, Monavari A, Mayne PD, Knerr I. Ventzke A, et al. Ir Med J. 2015 Nov-Dec;108(10):312-4. Ir Med J. 2015. PMID: 26817292

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