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Sandra Sirrs

Showing results (11-20 of 63) with videos related to

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Journal of Inherited Metabolic Disease|April 4, 2022
Lost in translation-Challenges in drug development for inherited metabolic diseasesRobin H Lachmann, Marc C Patterson, Sandra Sirrs
Healthcarepapers|July 7, 2023
Response to "Canadians Need Improved Access to Drugs for Rare Diseases, Not More Denial"Sandra Sirrs, Bashir Jiwani, Eric Lun, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2010
Multisystem disorder in late-onset chronic progressive external ophthalmoplegiaGerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Neurology|November 7, 2012
Child Neurology: Krabbe disease: a potentially treatable white matter disorderJennifer Gelinas, Pamela Liao, Anna Lehman, et al.
Neurology|October 19, 2016
Clinical Reasoning: A complicated case of MELASNikkie Randhawa, Laura Wilson, Sharanpal Mann, et al.
Journal of Medical Case Reports|August 1, 2012
Carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case reportPeter Ling, Douglas J Lee, Eric M Yoshida, et al.
International Journal of Endocrinology|July 13, 2011
Primary hyperparathyroidism: an overviewJessica Mackenzie-Feder, Sandra Sirrs, Donald Anderson, et al.
Leukemia & Lymphoma|November 3, 2005
Hypercalcemia due to all trans retinoic acid in the treatment of acute promyelocytic leukemia potentiated by voriconazoleMatthew T Bennett, Sandra Sirrs, Janice K Yeung, et al.
The Canadian Journal of Cardiology|November 1, 2015
The Genetic Challenges and Opportunities in Advanced Heart FailureFady Hannah-Shmouni, Sara B Seidelmann, Sandra Sirrs, et al.
Meta Gene|May 26, 2016
Identification of novel splice site mutation IVS9 + 1(G > A) and novel complex allele G355R/R359X in Type 1 Gaucher patients heterozygous for mutation N370SKourtnee Hoitsema, Dominick Amato, Aneal Khan, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|April 4, 2022
Lost in translation-Challenges in drug development for inherited metabolic diseasesRobin H Lachmann, Marc C Patterson, Sandra Sirrs
Healthcarepapers|July 7, 2023
Response to "Canadians Need Improved Access to Drugs for Rare Diseases, Not More Denial"Sandra Sirrs, Bashir Jiwani, Eric Lun, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 16, 2010
Multisystem disorder in late-onset chronic progressive external ophthalmoplegiaGerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Neurology|November 7, 2012
Child Neurology: Krabbe disease: a potentially treatable white matter disorderJennifer Gelinas, Pamela Liao, Anna Lehman, et al.
Neurology|October 19, 2016
Clinical Reasoning: A complicated case of MELASNikkie Randhawa, Laura Wilson, Sharanpal Mann, et al.
Journal of Medical Case Reports|August 1, 2012
Carnitine deficiency presenting with encephalopathy and hyperammonemia in a patient receiving chronic enteral tube feeding: a case reportPeter Ling, Douglas J Lee, Eric M Yoshida, et al.
International Journal of Endocrinology|July 13, 2011
Primary hyperparathyroidism: an overviewJessica Mackenzie-Feder, Sandra Sirrs, Donald Anderson, et al.
Leukemia & Lymphoma|November 3, 2005
Hypercalcemia due to all trans retinoic acid in the treatment of acute promyelocytic leukemia potentiated by voriconazoleMatthew T Bennett, Sandra Sirrs, Janice K Yeung, et al.
The Canadian Journal of Cardiology|November 1, 2015
The Genetic Challenges and Opportunities in Advanced Heart FailureFady Hannah-Shmouni, Sara B Seidelmann, Sandra Sirrs, et al.
Meta Gene|May 26, 2016
Identification of novel splice site mutation IVS9 + 1(G > A) and novel complex allele G355R/R359X in Type 1 Gaucher patients heterozygous for mutation N370SKourtnee Hoitsema, Dominick Amato, Aneal Khan, et al.
Pageof 7