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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1991 1
1993 2
1994 2
1995 1
1997 2
1998 1
1999 3
2000 1
2001 1
2003 3
2004 5
2005 4
2006 2
2007 2
2008 6
2009 2
2010 2
2011 3
2012 3
2013 3
2014 5
2015 3
2016 6
2017 2
2018 6
2019 6
2020 5
2021 5
2022 3
2023 3
2024 0

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82 results

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Page 1
Macrocytosis in Mitochondrial DNA Deletion Syndromes.
Almarzooqi F, Vallance H, Mezei M, Lehman A, Horvath G, Rakic B, Zypchen L, Mattman A. Almarzooqi F, et al. Among authors: vallance h. Acta Haematol. 2023;146(3):220-225. doi: 10.1159/000529311. Epub 2023 Feb 10. Acta Haematol. 2023. PMID: 36774923 Review.
Carrier testing for autosomal-recessive disorders.
Vallance H, Ford J. Vallance H, et al. Crit Rev Clin Lab Sci. 2003 Aug;40(4):473-97. doi: 10.1080/10408360390247832. Crit Rev Clin Lab Sci. 2003. PMID: 14582604 Review.
Coping with COVID: Preparing prescribers during the pandemic.
Ferner RE, Mason J, Vallance HK, Choudhary T, Marriott JF, Coleman JJ, Pontefract SK. Ferner RE, et al. Among authors: vallance hk. Br J Clin Pharmacol. 2022 May;88(5):2437-2440. doi: 10.1111/bcp.15153. Epub 2021 Dec 22. Br J Clin Pharmacol. 2022. PMID: 34806194 Free PMC article.
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG).
Carter MT, Srour M, Au PB, Buhas D, Dyack S, Eaton A, Inbar-Feigenberg M, Howley H, Kawamura A, Lewis SME, McCready E, Nelson TN, Vallance H; Canadian College of Medical Geneticists. Carter MT, et al. Among authors: vallance h. J Med Genet. 2023 Jun;60(6):523-532. doi: 10.1136/jmg-2022-108962. Epub 2023 Feb 23. J Med Genet. 2023. PMID: 36822643 Free PMC article.
Atypical cerebral palsy: genomics analysis enables precision medicine.
Matthews AM, Blydt-Hansen I, Al-Jabri B, Andersen J, Tarailo-Graovac M, Price M, Selby K, Demos M, Connolly M, Drögemoller B, Shyr C, Mwenifumbo J, Elliott AM, Lee J, Ghani A, Stöckler S, Salvarinova R, Vallance H, Sinclair G, Ross CJ, Wasserman WW, McKinnon ML, Horvath GA, Goez H, van Karnebeek CD; TIDE BC, United for Metabolic Diseases and the CAUSES Study. Matthews AM, et al. Among authors: vallance h. Genet Med. 2019 Jul;21(7):1621-1628. doi: 10.1038/s41436-018-0376-y. Epub 2018 Dec 13. Genet Med. 2019. PMID: 30542205 Free article.
Infantile cardioencephalopathy due to a COX15 gene defect: report and review.
Alfadhel M, Lillquist YP, Waters PJ, Sinclair G, Struys E, McFadden D, Hendson G, Hyams L, Shoffner J, Vallance HD. Alfadhel M, et al. Among authors: vallance hd. Am J Med Genet A. 2011 Apr;155A(4):840-4. doi: 10.1002/ajmg.a.33881. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21412973 Review.
Difficult airways: a 3D printing study with virtual fibreoptic endoscopy.
Ormandy D, Kolb B, Jayaram S, Burley O, Kyzas P, Vallance H, Vassiliou L. Ormandy D, et al. Among authors: vallance h. Br J Oral Maxillofac Surg. 2021 Feb;59(2):e65-e71. doi: 10.1016/j.bjoms.2020.08.045. Epub 2020 Aug 19. Br J Oral Maxillofac Surg. 2021. PMID: 33358011
Exome Sequencing and the Management of Neurometabolic Disorders.
Tarailo-Graovac M, Shyr C, Ross CJ, Horvath GA, Salvarinova R, Ye XC, Zhang LH, Bhavsar AP, Lee JJ, Drögemöller BI, Abdelsayed M, Alfadhel M, Armstrong L, Baumgartner MR, Burda P, Connolly MB, Cameron J, Demos M, Dewan T, Dionne J, Evans AM, Friedman JM, Garber I, Lewis S, Ling J, Mandal R, Mattman A, McKinnon M, Michoulas A, Metzger D, Ogunbayo OA, Rakic B, Rozmus J, Ruben P, Sayson B, Santra S, Schultz KR, Selby K, Shekel P, Sirrs S, Skrypnyk C, Superti-Furga A, Turvey SE, Van Allen MI, Wishart D, Wu J, Wu J, Zafeiriou D, Kluijtmans L, Wevers RA, Eydoux P, Lehman AM, Vallance H, Stockler-Ipsiroglu S, Sinclair G, Wasserman WW, van Karnebeek CD. Tarailo-Graovac M, et al. Among authors: vallance h. N Engl J Med. 2016 Jun 9;374(23):2246-55. doi: 10.1056/NEJMoa1515792. Epub 2016 May 25. N Engl J Med. 2016. PMID: 27276562 Free PMC article.
82 results