Monavari A - Search Results

1

Parental experience of enzyme replacement therapy for Hunter syndrome.

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

2

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

3

'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. Among authors: monavari a. Ir Med J. 2015 Nov-Dec;108(10):312-4. Ir Med J. 2015. PMID: 26817292

4

A review of anaesthetic outcomes in patients with genetically confirmed mitochondrial disorders.

Smith A, Dunne E, Mannion M, O'Connor C, Knerr I, Monavari AA, Hughes J, Eustace N, Crushell E. Smith A, et al. Among authors: monavari aa. Eur J Pediatr. 2017 Jan;176(1):83-88. doi: 10.1007/s00431-016-2813-8. Epub 2016 Nov 24. Eur J Pediatr. 2017. PMID: 27885500 Review.

5

Rotavirus Gastroenteritis is Associated with Increased Morbidity and Mortality in Children with Inherited Metabolic Disorders.

Smith A, Mannion M, O'Reilly P, Crushell E, Hughes J, Knerr I, Gavin P, Monavari A. Smith A, et al. Among authors: monavari a. Ir Med J. 2017 Apr 10;110(4):546. Ir Med J. 2017. PMID: 28665085

6

[No title available]

[No authors listed] [No authors listed] PMID: 32212602

7

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) in the Irish Paediatric Population.

Mesbah Z, Sing Ho K, Fitzsimons P, Monavari AA, Mayne PD, Crushell E. Mesbah Z, et al. Among authors: monavari aa. Ir Med J. 2019 Dec 16;112(10):1016. Ir Med J. 2019. PMID: 32311243

8

Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience.

Boruah R, Monavari AA, Conlon T, Murphy N, Stroiescu A, Ryan S, Hughes J, Knerr I, McDonnell C, Crushell E. Boruah R, et al. Among authors: monavari aa. J Clin Med. 2022 Mar 2;11(5):1366. doi: 10.3390/jcm11051366. J Clin Med. 2022. PMID: 35268460 Free PMC article.

9

Medium Chain Acyl-CoA Dehydrogenase Deficiency: 3 years of Newborn Screening.

Howard C, Gorman I, Crushell E, Knerr I, Hughes J, Boruah R, O'Grady L, Elsammak MY, Brady JJ, Monavari AA. Howard C, et al. Among authors: monavari aa. Ir Med J. 2023 Mar 23;116(3):743. Ir Med J. 2023. PMID: 37010499 No abstract available.

10

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

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