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Kinali, Maria
69
results:
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Online (69)
Mediatypes
Articles (Online) (44)
OpenAccess-fulltext (25)
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1
The Spectrum of MORC2-Related Disorders: A Potential Link t..:
Stafki, Seth A.
;
Turner, Johnnie
;
Littel, Hannah R.
...
Pediatric Neurology. 141 (2023) - p. 79-86 , 2023
Link:
https://doi.org/10.1016/..
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2
Neurodevelopmental and other phenotypes recurrently associa..:
Sewani, Soha
;
Azamian, Mahshid S.
;
Mendelsohn, Bryce A.
...
American Journal of Medical Genetics Part A. 194 (2023) 3 - p. , 2023
Link:
https://doi.org/10.1002/..
?
3
Genetic neuropathies presenting with CIDP-like features in ..:
Fernandez-Garcia, Miguel A.
;
Stettner, Georg M.
;
Kinali, Maria
...
Neuromuscular Disorders. 31 (2021) 2 - p. 113-122 , 2021
Link:
https://doi.org/10.1016/..
?
4
Machine learning with neuroimaging data to identify autism ..:
Song, Da-Yea
;
Topriceanu, Constantin-Cristian
;
Ilie-Ablachim, Denis C.
..
Neuroradiology. 63 (2021) 12 - p. 2057-2072 , 2021
Link:
https://doi.org/10.1007/..
?
5
Isolated bulbar palsy and dysphagia in children with respir..:
Zimmels, Stacey
;
Balfour‐Lynn, Ian M
;
Christodoulou, Loucas
...
Developmental Medicine & Child Neurology. 64 (2021) 4 - p. 518-522 , 2021
Link:
https://doi.org/10.1111/..
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6
Gene replacement ameliorates deficits in mouse and human mo..:
Mazarakis, Nicholas D
;
Kinali, Maria
;
Renieri, Alessandra
...
Brain. 143 (2020) 3 - p. 811-832 , 2020
Link:
https://doi.org/10.1093/..
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7
Phenotypic and genetic spectrum of epilepsy with myoclonic ..:
Tang, Shan
;
Addis, Laura
;
Smith, Anna
...
Epilepsia. 61 (2020) 5 - p. 995-1007 , 2020
Link:
https://doi.org/10.1111/..
?
8
A Case Series on Cardiac and Skeletal Involvement in Two Fa..:
Sri, Anita
;
Daubeney, Piers
;
Prasad, Sanjay
...
Case Reports in Pediatrics. 2019 (2019) - p. 1-7 , 2019
Link:
https://doi.org/10.1155/..
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9
The Interaction of Genetic Mutations in PARK2 and FA2H Caus..:
Benger, Matthew
;
Mankad, Kshitij
;
Proukakis, Christos
..
Frontiers in Neurology. 10 (2019) - p. , 2019
Link:
https://doi.org/10.3389/..
?
10
SCN2A mutation in an infant with Ohtahara syndrome and neur..:
Vlachou, Victoria
;
Larsen, Line
;
Pavlidou, Efterpi
...
Journal of Genetics. 98 (2019) 2 - p. , 2019
Link:
https://doi.org/10.1007/..
?
11
Autism spectrum disorder: prospects for treatment using gen..:
Benger, Matthew
;
Kinali, Maria
;
Mazarakis, Nicholas D.
Molecular Autism. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
12
Benign Infantile Epilepsy Mimicking Reflex Anoxic Seizures ..:
Vlachou, Victoria
;
Chu, Vivian
;
Pavlidou, Efterpi
...
The Indian Journal of Pediatrics. 85 (2017) 8 - p. 690-690 , 2017
Link:
https://doi.org/10.1007/..
?
13
Use of the Ketogenic Diet to Treat Intractable Epilepsy in ..:
Paleologou, Eleni
;
Ismayilova, Naila
;
Kinali, Maria
Journal of Clinical Medicine. 6 (2017) 6 - p. 56 , 2017
Link:
https://doi.org/10.3390/..
?
14
A novel PLP1 mutation associated with optic nerve enlargeme..:
Pavlidou, Efterpi
;
Ramachandran, Vijaya
;
Govender, Veronica
...
Brain and Development. 39 (2017) 3 - p. 271-274 , 2017
Link:
https://doi.org/10.1016/..
?
15
Delineation of the movement disorders associated withFOXG1m..:
Papandreou, Apostolos
;
Schneider, Ruth B.
;
Augustine, Erika F.
...
Neurology. 86 (2016) 19 - p. 1794-1800 , 2016
Link:
https://doi.org/10.1212/..
1-15