7 results
Case 14 - Pyridoxine-Dependent Epilepsy
- from Part V - Cases
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- Book:
- Neuromonitoring in Neonatal and Pediatric Critical Care
- Published online:
- 08 September 2022
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- 15 September 2022, pp 245-247
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Phenotypic and Genotypic Spectrum of Glucose Transporter-1 Deficiency Syndrome
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- Journal:
- Canadian Journal of Neurological Sciences / Volume 48 / Issue 6 / November 2021
- Published online by Cambridge University Press:
- 12 January 2021, pp. 826-830
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Chapter 3 - The Importance of Inborn Errors of Metabolism for Movement Disorders
- from Section I - General Principles and a Phenomenology-Based Approach to Movement Disorders and Inherited Metabolic Disorders
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- Book:
- Movement Disorders and Inherited Metabolic Disorders
- Published online:
- 24 September 2020
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- 01 October 2020, pp 26-42
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Chapter 28 - Disorders of Creatine Metabolism: Creatine Deficiency Syndromes and Movement Disorders
- from Section II - A Metabolism-Based Approach to Movement Disorders and Inherited Metabolic Disorders
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- Book:
- Movement Disorders and Inherited Metabolic Disorders
- Published online:
- 24 September 2020
- Print publication:
- 01 October 2020, pp 342-347
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Pyrroline-5-Carboxylate Reductase 2 Deficiency: A New Case and Review of the Literature
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- Journal:
- Canadian Journal of Neurological Sciences / Volume 47 / Issue 2 / March 2020
- Published online by Cambridge University Press:
- 10 January 2020, pp. 280-282
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Outcome of Patients With Inherited Neurotransmitter Disorders
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- Journal:
- Canadian Journal of Neurological Sciences / Volume 45 / Issue 5 / September 2018
- Published online by Cambridge University Press:
- 15 August 2018, pp. 571-576
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Prevalence of Genetic Disorders and GLUT1 Deficiency in a Ketogenic Diet Clinic
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- Journal:
- Canadian Journal of Neurological Sciences / Volume 45 / Issue 1 / January 2018
- Published online by Cambridge University Press:
- 16 November 2017, pp. 93-96
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