I agree that this site is using cookies. You can find further informations here.
X
Kinali, Maria
69  results:
Search for persons X
?
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/..
 
?
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/..
 
?
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/..
 
?
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/..
 
?
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