Greenberg CR - Search Results

1

Isolated sulfite oxidase deficiency: a founder mutation.

Mhanni AA, Greenberg CR, Spriggs EL, Agatep R, Sisk RR, Prasad C. Mhanni AA, et al. Among authors: greenberg cr. Cold Spring Harb Mol Case Stud. 2020 Dec 17;6(6):a005900. doi: 10.1101/mcs.a005900. Print 2020 Dec. Cold Spring Harb Mol Case Stud. 2020. PMID: 33335014 Free PMC article.

2

Genetic counseling in a busy pediatric metabolic practice.

Hartley JN, Greenberg CR, Mhanni AA. Hartley JN, et al. Among authors: greenberg cr. J Genet Couns. 2011 Feb;20(1):20-2. doi: 10.1007/s10897-010-9324-y. Epub 2010 Sep 14. J Genet Couns. 2011. PMID: 20839038

3

Reflex Seizures in a Patient with CDKL5 Deficiency Disorder.

Peikes T, Hartley JN, Mhanni AA, Greenberg CR, Appendino JP. Peikes T, et al. Among authors: greenberg cr. Can J Neurol Sci. 2019 Jul;46(4):482-485. doi: 10.1017/cjn.2019.29. Epub 2019 Apr 29. Can J Neurol Sci. 2019. PMID: 31030687 No abstract available.

4

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (HHH) presenting with acute fulminant hepatic failure.

Mhanni AA, Chan A, Collison M, Seifert B, Lehotay DC, Sokoro A, Huynh HQ, Greenberg CR. Mhanni AA, et al. Among authors: greenberg cr. J Pediatr Gastroenterol Nutr. 2008 Mar;46(3):312-5. doi: 10.1097/MPG.0b013e318145a8e5. J Pediatr Gastroenterol Nutr. 2008. PMID: 18376250

5

Genetic testing of children at risk for adult onset conditions: when is testing indicated?

Lwiwski N, Greenberg CR, Mhanni AA. Lwiwski N, et al. Among authors: greenberg cr. J Genet Couns. 2008 Dec;17(6):523-5. doi: 10.1007/s10897-008-9161-4. Epub 2008 Jul 8. J Genet Couns. 2008. PMID: 18607700

6

Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder.

Sharma AP, Greenberg CR, Prasad AN, Prasad C. Sharma AP, et al. Among authors: greenberg cr. Pediatr Nephrol. 2007 Dec;22(12):2097-103. doi: 10.1007/s00467-007-0604-1. Epub 2007 Sep 14. Pediatr Nephrol. 2007. PMID: 17874135

7

Trends in telehealth versus on-site clinical genetics appointments in Manitoba: a comparative study.

Elliott AM, Mhanni AA, Marles SL, Greenberg CR, Chudley AE, Nyhof GC, Chodirker BN. Elliott AM, et al. Among authors: greenberg cr. J Genet Couns. 2012 Apr;21(2):337-44. doi: 10.1007/s10897-011-9406-5. Epub 2011 Oct 15. J Genet Couns. 2012. PMID: 21997346

8

Outcome of perinatal hypophosphatasia in manitoba mennonites: a retrospective cohort analysis.

Leung EC, Mhanni AA, Reed M, Whyte MP, Landy H, Greenberg CR. Leung EC, et al. Among authors: greenberg cr. JIMD Rep. 2013;11:73-8. doi: 10.1007/8904_2013_224. Epub 2013 Apr 12. JIMD Rep. 2013. PMID: 23580367 Free PMC article.

9

Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population.

Triggs-Raine B, Dyck T, Boycott KM, Innes AM, Ober C, Parboosingh JS, Botkin A, Greenberg CR, Spriggs EL. Triggs-Raine B, et al. Among authors: greenberg cr. Mol Genet Genomic Med. 2016 Jan 19;4(3):312-21. doi: 10.1002/mgg3.206. eCollection 2016 May. Mol Genet Genomic Med. 2016. PMID: 27247959 Free PMC article.

10

Ketogenic diet in Alpers-Huttenlocher syndrome.

Joshi CN, Greenberg CR, Mhanni AA, Salman MS. Joshi CN, et al. Among authors: greenberg cr. Pediatr Neurol. 2009 Apr;40(4):314-6. doi: 10.1016/j.pediatrneurol.2008.10.023. Pediatr Neurol. 2009. PMID: 19302948

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