Nagy LL - Search Results

1

New Paradigm for the Treatment of Glucose Transporter 1 Deficiency Syndrome: Low Glycemic Index Diet and Modified High Amylopectin Cornstarch.

Almuqbil M, Go C, Nagy LL, Pai N, Mamak E, Mercimek-Mahmutoglu S. Almuqbil M, et al. Among authors: nagy ll. Pediatr Neurol. 2015 Sep;53(3):243-6. doi: 10.1016/j.pediatrneurol.2015.06.018. Epub 2015 Jun 26. Pediatr Neurol. 2015. PMID: 26216499

2

The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.

Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S. Roscher A, et al. Mol Genet Metab. 2014 Nov;113(3):171-6. doi: 10.1016/j.ymgme.2014.09.005. Epub 2014 Sep 21. Mol Genet Metab. 2014. PMID: 25266922

3

Lysine-restricted diet and mild cerebral serotonin deficiency in a patient with pyridoxine-dependent epilepsy caused by ALDH7A1 genetic defect.

Mercimek-Mahmutoglu S, Corderio D, Nagy L, Mutch C, Carter M, Struys E, Kyriakopoulou L. Mercimek-Mahmutoglu S, et al. Mol Genet Metab Rep. 2014 Apr 1;1:124-128. doi: 10.1016/j.ymgmr.2014.02.001. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896080 Free PMC article.

4

Use of waxy maize heat modified starch in the treatment of children between 2 and 5 years with glycogen storage disease type I: A retrospective study.

Hijazi G, Pai N, Nagy LL, Herd S, Dickson J, Ram M, Inbar-Feigenberg M. Hijazi G, et al. Among authors: nagy ll. Mol Genet Metab Rep. 2019 Nov 6;21:100536. doi: 10.1016/j.ymgmr.2019.100536. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31844626 Free PMC article.

5

Long-Term Treatment of Lipoprotein Lipase Deficiency with Medium-Chain Triglyceride-Enriched Diet: A Case Series.

Aljouda L, Nagy L, Schulze A. Aljouda L, et al. Nutrients. 2023 Aug 11;15(16):3535. doi: 10.3390/nu15163535. Nutrients. 2023. PMID: 37630727 Free PMC article.

6

Management and Outcomes of Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD Deficiency): A Retrospective Chart Review.

Al Bandari M, Nagy L, Cruz V, Hewson S, Hossain A, Inbar-Feigenberg M. Al Bandari M, et al. Int J Neonatal Screen. 2024 Mar 30;10(2):29. doi: 10.3390/ijns10020029. Int J Neonatal Screen. 2024. PMID: 38651394 Free PMC article.

7

Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency.

Iverson R, Taljaard M, Geraghty MT, Pugliese M, Tingley K, Coyle D, Kronick JB, Wilson K, Austin V, Brunel-Guitton C, Buhas D, Butcher NJ, Chan AKJ, Dyack S, Goobie S, Greenberg CR, Jain-Ghai S, Inbar-Feigenberg M, Karp N, Kozenko M, Langley E, Lines M, Little J, MacKenzie J, Maranda B, Mercimek-Andrews S, Mhanni A, Mitchell JJ, Nagy L, Offringa M, Pender A, Potter M, Prasad C, Ratko S, Salvarinova R, Schulze A, Siriwardena K, Sondheimer N, Sparkes R, Stockler-Ipsiroglu S, Tapscott K, Trakadis Y, Turner L, Van Karnebeek C, Vandersteen A, Walia JS, Wilson BJ, Yu AC, Potter BK, Chakraborty P. Iverson R, et al. BMC Pediatr. 2024 Jan 13;24(1):37. doi: 10.1186/s12887-023-04393-4. BMC Pediatr. 2024. PMID: 38216926 Free PMC article.

8

Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease.

Khangura SD, Karaceper MD, Trakadis Y, Mitchell JJ, Chakraborty P, Tingley K, Coyle D, Grosse SD, Kronick JB, Laberge AM, Little J, Prasad C, Sikora L, Siriwardena K, Sparkes R, Speechley KN, Stockler S, Wilson BJ, Wilson K, Zayed R, Potter BK; Canadian Inherited Metabolic Diseases Research Network. Khangura SD, et al. BMC Pediatr. 2015 Feb 13;15:7. doi: 10.1186/s12887-015-0323-x. BMC Pediatr. 2015. PMID: 25886474 Free PMC article. Review.

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