Research graph
References from Pediatric stroke in inborn errors of metabolism: clinical characteristics, neuroimaging features, and short-term outcomes. Local targets link to admitted publications; unresolved targets remain external evidence.
Pediatric stroke: overview and recent updates
10.14336/ad.2021.0219 · 2021 · External reference
Metabolic stroke in childhood: diagnostic approach and suggestions for therapy
10.3233/jpn-2010-0404 · 2010 · External reference
Metabolic stroke or stroke-like lesion: peculiarities of a phenomenon
10.1016/j.jns.2020.116726 · 2020 · External reference
Mitochondrial metabolic stroke: phenotype and genetics of stroke-like episodes
10.1016/j.jns.2019.03.021 · 2019 · External reference
Taurine supplementation for prevention of stroke-like episodes in MELAS: a multicentre, open-label, 52-week phase III trial
10.1136/jnnp-2018-317964 · 2019 · External reference
A case report of Homocystinuria with dystonia and stroke
10.1177/2329048x14545870 · 2014 · External reference
Unique Neuroradiological findings in propionic academia
10.1016/j.radcr.2018.08.011 · 2018 · External reference
Acute ischemic stroke in children versus young adults
10.1002/ana.22427 · 2011 · External reference
Updated classification of epileptic seizures: position paper of the international league against epilepsy
10.1111/epi.18338 · 2025 · External reference
The impact of consanguinity on the Frequency of inborn errors of metabolism
10.1016/j.ymgmr.2017.11.004 · 2018 · External reference
Inherited metabolic causes of stroke in children: mechanisms, types, and management
10.3389/fneur.2021.633119 · 2021 · External reference
Stroke-like episodes in inherited Neurometabolic disorders
10.3390/metabo12100929 · 2022 · External reference
Succinic Semialdehyde dehydrogenase deficiency – a rare cause of metabolic stroke
10.56310/pjns.v17i02.180 · 2022 · External reference
Molybdenum cofactor deficiency (MoCD) masquerading as stroke-like episodes
10.1007/s12098-023-05002-z · 2024 · External reference
Biallelic GGGCC repeat expansion leading to NAXE-related mitochondrial encephalopathy
10.1038/s41525-024-00429-5 · 2024 · External reference
NAXE gene mutation-related progressive encephalopathy: a case report and literature review
10.1097/md.0000000000027548 · 2021 · External reference
Sengers syndrome and AGK-related disorders - minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases
10.1016/j.ymgme.2023.107626 · 2023 · External reference
MELAS syndrome: clinical manifestations, pathogenesis, and treatment options
10.1016/j.ymgme.2015.06.004 · 2015 · External reference
Risk factors for recurrent arterial ischemic stroke in children and young adults
10.3390/brainsci10010024 · 2020 · External reference
Recurrent stroke like episodes secondary to ornithine Transcarbamylase deficiency
10.1007/s12098-020-03193-3 · 2020 · External reference
Clinical characteristics and diagnostic clues to Neurometabolic causes of dystonia
10.1016/j.jns.2020.117167 · 2020 · External reference
Ataxia in neurometabolic disorders
10.3390/metabo13010047 · 2022 · External reference
A rare case of propionic Acidemia in a six months female child
10.29271/jcpsp.2022.supp2.s180 · 2022 · External reference
Impaired lipolysis in propionic Acidemia: a new metabolic myopathy?
10.1002/jmd2.12113 · 2020 · External reference
Peripheral neuropathy associated with mitochondrial disease in children
10.1111/j.1469-8749.2012.04271.x · 2012 · External reference
Peripheral nerve involvement in classic homocystinuria: an unusual association
10.1136/bcr-2016-216255 · 2016 · External reference
Ocular characteristics of a 6-year-old boy with molybdenum cofactor deficiency type B
10.1016/j.ajoc.2022.101586 · 2022 · External reference
Inherited Paediatric Neurometabolic disorders, can brain magnetic resonance imaging predict?
10.17712/nsj.2020.5.20200072 · 2020 · External reference
MR neuroimaging in pediatric inborn errors of metabolism
10.3390/diagnostics12040861 · 2022 · External reference
Angiopathy and stroke associated with homocystinuria in childhood
10.1177/15385744221144978 · 2023 · External reference