Rockman-Greenberg C - Search Results

1

Neonatal hypoglycemia and the CPT1A P479L variant in term newborns: A retrospective cohort study of Inuit newborns from Kivalliq Nunavut.

Collins SA, Hildes-Ripstein GE, Thompson JR, Edmunds S, Miners A, Rockman-Greenberg C, Arbour L. Collins SA, et al. Paediatr Child Health. 2020 Apr 3;26(4):218-227. doi: 10.1093/pch/pxaa039. eCollection 2021 Jul. Paediatr Child Health. 2020. PMID: 34131458 Free PMC article.

2

Association of the CPT1A p.P479L Metabolic Gene Variant With Childhood Respiratory and Other Infectious Illness in Nunavut.

Collins SA, Edmunds S, Akearok GH, Thompson JR, Erickson AC, Hildes-Ripstein E, Miners A, Somerville M, Goldfarb DM, Rockman-Greenberg C, Arbour L. Collins SA, et al. Front Pediatr. 2021 Jul 6;9:678553. doi: 10.3389/fped.2021.678553. eCollection 2021. Front Pediatr. 2021. PMID: 34295859 Free PMC article.

3

Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases.

Jilkina O, Thompson JR, Kwan L, Van Caeseele P, Rockman-Greenberg C, Schroeder ML. Jilkina O, et al. Mol Genet Metab Rep. 2014 Aug 7;1:324-333. doi: 10.1016/j.ymgmr.2014.07.003. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896105 Free PMC article.

4

Blood acylcarnitine levels in normal newborns and heterozygotes for medium-chain acyl-CoA dehydrogenase deficiency: a relationship between genotype and biochemical phenotype?

Lehotay DC, LePage J, Thompson JR, Rockman-Greenberg C. Lehotay DC, et al. J Inherit Metab Dis. 2004;27(1):81-8. doi: 10.1023/B:BOLI.0000016636.79030.ad. J Inherit Metab Dis. 2004. PMID: 14970748

5

Social paediatrics: From 'lip service' to the health and well-being of Canada's children and youth.

Daneman D, Kellner J, Bernstein M, Dow K, Dugas MA, Duffy C, Eddy A, Filler G, Frappier JY, Gilmour S, Givelichian L, Huang L, Rockman-Greenberg C, Shevell M, Vardy C, Walti H, Orrbine E, Williams M. Daneman D, et al. Paediatr Child Health. 2013 Aug;18(7):351-2. Paediatr Child Health. 2013. PMID: 24421706 Free PMC article. No abstract available.

6

Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis.

Rubin TS, Rockman-Greenberg C, Van Caeseele P, Cuvelier GDE, Kwan L, Schroeder ML. Rubin TS, et al. J Clin Immunol. 2018 Oct;38(7):742-744. doi: 10.1007/s10875-018-0555-2. Epub 2018 Oct 4. J Clin Immunol. 2018. PMID: 30288645 No abstract available.

7

Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan.

Sokoro AA, Lepage J, Antonishyn N, McDonald R, Rockman-Greenberg C, Irvine J, Lehotay DC. Sokoro AA, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S275-81. doi: 10.1007/s10545-010-9148-9. Epub 2010 Jun 24. J Inherit Metab Dis. 2010. PMID: 20574716

8

Outcome of the glutaric aciduria type 1 (GA1) newborn screening program in Manitoba: 1980-2020.

Mhanni A, Aylward N, Boy N, Martin B, Sharma A, Rockman-Greenberg C. Mhanni A, et al. Mol Genet Metab Rep. 2020 Nov 25;25:100666. doi: 10.1016/j.ymgmr.2020.100666. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33299796 Free PMC article.

9

Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease.

Mhanni AA, Kozenko M, Hartley JN, Deneau M, El-Matary W, Rockman-Greenberg C. Mhanni AA, et al. Mol Genet Metab Rep. 2015 Dec 29;6:13-5. doi: 10.1016/j.ymgmr.2015.12.001. eCollection 2016 Mar. Mol Genet Metab Rep. 2015. PMID: 27014572 Free PMC article.

10

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.

Karaceper MD, Khangura SD, Wilson K, Coyle D, Brownell M, Davies C, Dodds L, Feigenbaum A, Fell DB, Grosse SD, Guttmann A, Hawken S, Hayeems RZ, Kronick JB, Laberge AM, Little J, Mhanni A, Mitchell JJ, Nakhla M, Potter M, Prasad C, Rockman-Greenberg C, Sparkes R, Stockler S, Ueda K, Vallance H, Wilson BJ, Chakraborty P, Potter BK; Canadian Inherited Metabolic Diseases Research Network (CIMDRN). Karaceper MD, et al. Orphanet J Rare Dis. 2019 Mar 22;14(1):70. doi: 10.1186/s13023-019-1001-0. Orphanet J Rare Dis. 2019. PMID: 30902101 Free PMC article.

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