l carnitine deficiency radiology

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Frontiers

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Brain MRI of a 45-year-old female presenting with slowly progressive

Brain MRI of a 45-year-old female presenting with slowly progressive

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Systemic primary carnitine deficiency with hypoglycemic encephalopathy

Systemic primary carnitine deficiency with hypoglycemic encephalopathy

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Congenital Inborn Errors of Metabolism: Clinical and Imaging Pearls

Congenital Inborn Errors of Metabolism: Clinical and Imaging Pearls

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Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency - a cardiac magnetic resonance study

Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency - a cardiac magnetic resonance study

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Brain MRI scans of the patient with primary carnitine deficiency and

Brain MRI scans of the patient with primary carnitine deficiency and

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NEW $Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome | Italian Journal of Pediatrics$

Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome | Italian Journal of Pediatrics

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Unmasking Primary Carnitine Deficiency as a Mimic of Hypertrophic Cardiomyopathy

Unmasking Primary Carnitine Deficiency as a Mimic of Hypertrophic Cardiomyopathy

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First Case Report of Primary Carnitine Deficiency Manifested as Intellectual Disability and Autism Spectrum Disorder

First Case Report of Primary Carnitine Deficiency Manifested as Intellectual Disability and Autism Spectrum Disorder

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Systemic Primary Carnitine Deficiency Presenting With Substantia Nigra and Basal Ganglia Injury: A Case Report - Saito - 2025 - JIMD Reports

Systemic Primary Carnitine Deficiency Presenting With Substantia Nigra and Basal Ganglia Injury: A Case Report - Saito - 2025 - JIMD Reports

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Effect of l-carnitine supplementation on muscle cramps induced by stroke: A case report

Effect of l-carnitine supplementation on muscle cramps induced by stroke: A case report

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Carnitine Deficiency: What You Need to Know

Carnitine Deficiency: What You Need to Know

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Glutaric Aciduria Type 1

Glutaric Aciduria Type 1

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Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations

Brain imaging in mitochondrial respiratory chain deficiency: combination of brain MRI features as a useful tool for genotype/phenotype correlations

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MRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report - Yilmaz - 2015 - Journal of Neuroimaging

MRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report - Yilmaz - 2015 - Journal of Neuroimaging

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Hyperammonemic Encephalopathy Caused by Carnitine Deficiency

Hyperammonemic Encephalopathy Caused by Carnitine Deficiency

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Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development - Shelihan - 2022 - JIMD Reports

Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development - Shelihan - 2022 - JIMD Reports

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Left ventricular cardiomyopathy due to CPT II hereditary deficiency. Keys to an infrequent diagnosis

Left ventricular cardiomyopathy due to CPT II hereditary deficiency. Keys to an infrequent diagnosis

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Systematic Approach to Diagnose Inborn Neurometabolic Disorders

Systematic Approach to Diagnose Inborn Neurometabolic Disorders

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Primary carnitine deficiency cardiomyopathy

Primary carnitine deficiency cardiomyopathy

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