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Journal of Inherited Metabolic Disease
|
April 4, 2022
Lost in translation-Challenges in drug development for inherited metabolic diseases
Robin 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 ophthalmoplegia
Gerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Neurology
|
November 7, 2012
Child Neurology: Krabbe disease: a potentially treatable white matter disorder
Jennifer Gelinas, Pamela Liao, Anna Lehman, et al.
Neurology
|
October 19, 2016
Clinical Reasoning: A complicated case of MELAS
Nikkie 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 report
Peter Ling, Douglas J Lee, Eric M Yoshida, et al.
International Journal of Endocrinology
|
July 13, 2011
Primary hyperparathyroidism: an overview
Jessica 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 voriconazole
Matthew 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 Failure
Fady 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 N370S
Kourtnee Hoitsema, Dominick Amato, Aneal Khan, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 63) with videos related to
Sort By:
Page
of 7
Journal of Inherited Metabolic Disease
|
April 4, 2022
Lost in translation-Challenges in drug development for inherited metabolic diseases
Robin 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 ophthalmoplegia
Gerald Pfeffer, Sandra Sirrs, N Kevin Wade, et al.
Neurology
|
November 7, 2012
Child Neurology: Krabbe disease: a potentially treatable white matter disorder
Jennifer Gelinas, Pamela Liao, Anna Lehman, et al.
Neurology
|
October 19, 2016
Clinical Reasoning: A complicated case of MELAS
Nikkie 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 report
Peter Ling, Douglas J Lee, Eric M Yoshida, et al.
International Journal of Endocrinology
|
July 13, 2011
Primary hyperparathyroidism: an overview
Jessica 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 voriconazole
Matthew 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 Failure
Fady 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 N370S
Kourtnee Hoitsema, Dominick Amato, Aneal Khan, et al.
Page
of 7