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Sandy Ayoub

Showing results (1-10 of 6) with videos related to

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Medical Education|December 24, 2019
Reasonable adjustments beyond medical schoolCarys Mangan, Sandy Ayoub
Medical Teacher|November 15, 2019
Telephone communication: A new Mini-CEX?Chantal Liu, Sandy Ayoub
Emergency Medicine Australasia : EMA|September 16, 2020
Interventions to support Choosing Wisely for coagulation studies in the emergency departmentMandeep S Kalsi, Chuan Tai Foo, Parisa Farzanehfar, et al.
Disability and Rehabilitation|April 1, 2020
The positive and the negative impacts of spasticity in patients with long-term neurological conditions: an observational studySandy Ayoub, Jared G Smith, Isabel Cary, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
American Journal of Medical Genetics. Part A|February 25, 2020
Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers-Danlos syndromeSandy Ayoub, Neeti Ghali, Chloe Angwin, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Medical Education|December 24, 2019
Reasonable adjustments beyond medical schoolCarys Mangan, Sandy Ayoub
Medical Teacher|November 15, 2019
Telephone communication: A new Mini-CEX?Chantal Liu, Sandy Ayoub
Emergency Medicine Australasia : EMA|September 16, 2020
Interventions to support Choosing Wisely for coagulation studies in the emergency departmentMandeep S Kalsi, Chuan Tai Foo, Parisa Farzanehfar, et al.
Disability and Rehabilitation|April 1, 2020
The positive and the negative impacts of spasticity in patients with long-term neurological conditions: an observational studySandy Ayoub, Jared G Smith, Isabel Cary, et al.
The Journal of Clinical Endocrinology and Metabolism|February 16, 2020
Loss-of-Function Variants in TBC1D32 Underlie Syndromic HypopituitarismJohanna Hietamäki, Louise C Gregory, Sandy Ayoub, et al.
American Journal of Medical Genetics. Part A|February 25, 2020
Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers-Danlos syndromeSandy Ayoub, Neeti Ghali, Chloe Angwin, et al.
Pageof 1