Prasad C - Search Results

1

Two cases of carbonic anhydrase VA deficiency-An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcome.

Marwaha A, Ibrahim J, Rice T, Hamwi N, Rupar CA, Cresswell D, Prasad C, Schulze A. Marwaha A, et al. Among authors: prasad c. JIMD Rep. 2020 Oct 1;57(1):9-14. doi: 10.1002/jmd2.12171. eCollection 2021 Jan. JIMD Rep. 2020. PMID: 33473334 Free PMC article.

2

Use of complementary and alternative medicine in patients with inborn errors of metabolism: A single-center study.

Tao J, Rupar CA, Miller MR, Ratko S, Prasad C. Tao J, et al. Among authors: prasad c. JIMD Rep. 2019 Dec 18;51(1):105-112. doi: 10.1002/jmd2.12089. eCollection 2020 Jan. JIMD Rep. 2019. PMID: 32071845 Free PMC article.

3

Biochemical and Hematologic Manifestations of Gastric Intrinsic Factor (GIF) Deficiency: A Treatable Cause of B12 Deficiency in the Old Order Mennonite Population of Southwestern Ontario.

Ferrand A, Siu VM, Rupar CA, Napier MP, Al-Dirbashi OY, Chakraborty P, Prasad C. Ferrand A, et al. Among authors: prasad c. JIMD Rep. 2015;18:69-77. doi: 10.1007/8904_2014_351. Epub 2014 Oct 12. JIMD Rep. 2015. PMID: 25308559 Free PMC article.

4

Methylenetetrahydrofolate reductase (MTHFR) deficiency and infantile epilepsy.

Prasad AN, Rupar CA, Prasad C. Prasad AN, et al. Among authors: prasad c. Brain Dev. 2011 Oct;33(9):758-69. doi: 10.1016/j.braindev.2011.05.014. Epub 2011 Jul 22. Brain Dev. 2011. PMID: 21778025 Review.

5

Coma, hyperammonemia, metabolic acidosis, and mutation: lessons learned in the acute management of late onset urea cycle disorders.

Iyer H, Sen M, Prasad C, Rupar CA, Lindsay RM. Iyer H, et al. Among authors: prasad c. Hemodial Int. 2012 Jan;16(1):95-100. doi: 10.1111/j.1542-4758.2011.00591.x. Hemodial Int. 2012. PMID: 22099885

6

Severe phenotypic spectrum of mevalonate kinase deficiency with minimal mevalonic aciduria.

Prasad C, Salvadori MI, Rupar CA. Prasad C, et al. Mol Genet Metab. 2012 Dec;107(4):756-9. doi: 10.1016/j.ymgme.2012.10.019. Epub 2012 Oct 24. Mol Genet Metab. 2012. PMID: 23146290

7

Pitfalls in Genetic Testing for Consanguineous Pediatric Populations.

Saleh M, Colaiacovo S, Napier MP, Prasad AN, Rupar CA, Prasad C. Saleh M, et al. Among authors: prasad an, prasad c. Case Rep Genet. 2022 May 25;2022:9393042. doi: 10.1155/2022/9393042. eCollection 2022. Case Rep Genet. 2022. PMID: 35663206 Free PMC article.

8

An Unexpected Finding of Hepatosplenomegaly in a Pediatric Patient.

Barootes HC, Prasad C, Rupar CA, Ashok D. Barootes HC, et al. Among authors: prasad c. Clin Pediatr (Phila). 2022 Jan;61(1):81-85. doi: 10.1177/00099228211059668. Epub 2021 Nov 18. Clin Pediatr (Phila). 2022. PMID: 34789027 Free PMC article.

9

Amish microcephaly: Long-term survival and biochemical characterization.

Siu VM, Ratko S, Prasad AN, Prasad C, Rupar CA. Siu VM, et al. Among authors: prasad an, prasad c. Am J Med Genet A. 2010 Jul;152A(7):1747-51. doi: 10.1002/ajmg.a.33373. Am J Med Genet A. 2010. PMID: 20583149

10

Asymptomatic critical hypoglycaemia: a dangerous presentation of glycogen storage disease type Ib in infancy.

Bock DE, Rupar CA, Prasad C. Bock DE, et al. Among authors: prasad c. Acta Paediatr. 2011 Sep;100(9):e130-2. doi: 10.1111/j.1651-2227.2011.02208.x. Epub 2011 Mar 15. Acta Paediatr. 2011. PMID: 21352356

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