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Author Details
Full Name
Marios Kaliakatsos
Affiliation
Great Ormond Street Hospital for Children
ORCID
Career Start Year
2006
Papers
34
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36864284
A novel ELP1 mutation impairs the function of the Elongator complex and causes a severe neurodevelopmental phenotype.
J Hum Genet
2023
37557958
Translating metagenomics into clinical practice for complex paediatric neurological presentations.
J Infect
2023
37012667
Acute necrotizing encephalopathy of childhood: Prevention is better than cure especially if the cure remains elusive.
Dev Med Child Neurol
2023
37041080
Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic <i>SLC30A9</i> Pathogenic Variants.
Neurology
2023
35015932
Clinical features, investigations, and outcomes of pediatric limbic encephalitis: A multicenter study.
Ann Clin Transl Neurol
2022
35561731
Neurostimulation devices for children: lessons learned.
Lancet Child Adolesc Health
2022
36177038
Case report: Novel treatment regimen for <i>enterovirus</i> encephalitis in SCID.
Front Immunol
2022
34466801
Pathogenic <i>NR2F1</i> variants cause a developmental ocular phenotype recapitulated in a mutant mouse model.
Brain Commun
2021
33681649
Proposal to optimize evaluation and treatment of Febrile infection-related epilepsy syndrome (FIRES): A Report from FIRES workshop.
Epilepsia Open
2021
32554502
Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Proc Natl Acad Sci U S A
2020
33506622
Anakinra usage in febrile infection related epilepsy syndrome: an international cohort.
Ann Clin Transl Neurol
2020
32044693
Epilepsy in paediatric patients with Parry-Romberg syndrome: A review of the literature.
Seizure
2020
32096284
KIF1A-related disorders in children: A wide spectrum of central and peripheral nervous system involvement.
J Peripher Nerv Syst
2020
32651625
Non-congenital viral infections of the central nervous system: from the immunocompetent to the immunocompromised child.
Pediatr Radiol
2020
32875551
Diagnostic algorithm for children presenting with epilepsia partialis continua.
Epilepsia
2020
30379117
Paediatric MOG antibody-associated ADEM with complex movement disorder: A case report.
Mult Scler
2019
31259196
Two Cases of Guillain-Barré Syndrome Variants Presenting With Dysautonomia.
Child Neurol Open
2019
31446001
Centromedian thalamic nuclei deep brain stimulation and Anakinra treatment for FIRES - Two different outcomes.
Eur J Paediatr Neurol
2019
30854647
The spectrum of neuroimaging findings in febrile infection-related epilepsy syndrome (FIRES): A literature review.
Epilepsia
2019
29759327
Immunotherapy-responsive childhood neurodegeneration with systemic and central nervous system inflammation.
Eur J Paediatr Neurol
2018
27770235
Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis.
Acta Neuropathol
2017
27041136
In response: Comment on outcome following multiple subpial transection in Landau-Kleffner syndrome and related regression.
Epilepsia
2016
26371981
An unusual presentation of paediatric Listeria meningitis with selective spinal grey matter involvement and acute demyelinating polyneuropathy.
Eur J Paediatr Neurol
2016
26915897
Thickening of the optic nerves in metachromatic leucodystrophy: A new MRI finding.
Neuroradiol J
2016
26337264
Outcome following multiple subpial transection in Landau-Kleffner syndrome and related regression.
Epilepsia
2015
24247994
Reversible vigabatrin-induced life-threatening encephalopathy.
JAMA Neurol
2014
22729384
Hypertrophic olivary degeneration on magnetic resonance imaging in mitochondrial syndromes associated with POLG and SURF1 mutations.
J Neurol
2013
25877636
Acute disseminated encephalomyelitis associated with positive voltage gated potassium channel complex antibody.
Mult Scler Relat Disord
2013
19747908
Development of novel microarray methodology for the study of mutations in the SERPINA1 and ADRB2 genes--their association with Obstructive Pulmonary Disease and Disseminated Bronchiectasis in Greek patients.
Clin Biochem
2010
20686492
Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.
J Hum Genet
2010
18452398
Association of the CALM1 core promoter polymorphism with knee osteoarthritis in patients of Greek origin.
Genet Test
2008
17489851
Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
Clin Genet
2007
17509552
Development of a novel microarray methodology for the study of SNPs in the promoter region of the TNF-alpha gene: their association with obstructive pulmonary disease in Greek patients.
Clin Biochem
2007
16377215
Asporin and knee osteoarthritis in patients of Greek origin.
Osteoarthritis Cartilage
2006
1 - 34 of 34
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