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Athina Ververi
Athina Ververi
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在 athinaververi.org 的电子邮件经过验证
标题
引用次数
引用次数
年份
Childhood autism and associated comorbidities
DI Zafeiriou, A Ververi, E Vargiami
Brain and development 29 (5), 257-272, 2007
3052007
Autism spectrum disorders: the quest for genetic syndromes
DI Zafeiriou, A Ververi, V Dafoulis, E Kalyva, E Vargiami
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013
1212013
Childhood autism and auditory system abnormalities
M Hitoglou, A Ververi, A Antoniadis, DI Zafeiriou
Pediatric neurology 42 (5), 309-314, 2010
1162010
The serotonergic system: its role in pathogenesis and early developmental treatment of autism
DI Zafeiriou, A Ververi, E Vargiami
Current neuropharmacology 7 (2), 150-157, 2009
1032009
KIF1A‐related disorders in children: A wide spectrum of central and peripheral nervous system involvement
T Nemani, D Steel, M Kaliakatsos, C DeVile, A Ververi, R Scott, S Getov, ...
Journal of the Peripheral Nervous System 25 (2), 117-124, 2020
512020
Clinical and laboratory data in a sample of Greek children with autism spectrum disorders
A Ververi, E Vargiami, V Papadopoulou, D Tryfonas, DI Zafeiriou
Journal of autism and developmental disorders 42, 1470-1476, 2012
472012
Tyrosine hydroxylase deficiency with severe clinical course
DI Zafeiriou, MA Willemsen, MM Verbeek, E Vargiami, A Ververi, ...
Molecular genetics and metabolism 97 (1), 18-20, 2009
462009
MR spectroscopy and serial magnetic resonance imaging in a patient with mitochondrial cystic leukoencephalopathy due to complex I deficiency and NDUFV1 mutations and mild …
DI Zafeiriou, RJT Rodenburg, H Scheffer, LP van den Heuvel, ...
Neuropediatrics 39 (03), 172-175, 2008
412008
L-2-Hydroxyglutaric aciduria presenting with severe autistic features
DI Zafeiriou, A Ververi, GS Salomons, E Vargiami, D Haas, ...
Brain and Development 30 (4), 305-307, 2008
382008
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
R Alharatani, A Ververi, A Beleza-Meireles, W Ji, E Mis, QT Patterson, ...
Human molecular genetics 29 (11), 1900-1921, 2020
342020
Bi-allelic variants in the GPI transamidase subunit PIGK cause a neurodevelopmental syndrome with hypotonia, cerebellar atrophy, and epilepsy
TTM Nguyen, Y Murakami, S Mobilio, M Niceta, G Zampino, C Philippe, ...
The American Journal of Human Genetics 106 (4), 484-495, 2020
302020
Brainstem auditory evoked potentials in boys with autism: still searching for the hidden truth
A Ververi, E Vargiami, V Papadopoulou, D Tryfonas, D Zafeiriou
Iranian Journal of Child Neurology 9 (2), 21, 2015
232015
Phenotypic spectrum associated with de novo mutations in QRICH1 gene
A Ververi, M Splitt, JCS Dean, DDD Study, AF Brady
Clinical genetics 93 (2), 286-292, 2018
192018
Severe clinical presentation in monozygotic twins with 10p15. 3 microdeletion syndrome
E Vargiami, A Ververi, M Kyriazi, E Papathanasiou, G Gioula, S Gerou, ...
American Journal of Medical Genetics Part A 164 (3), 764-768, 2014
182014
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation
DI Zafeiriou, F Lehmann-Horn, E Vargiami, E Teflioudi, A Ververi, ...
european journal of paediatric neurology 13 (2), 191-193, 2009
142009
Pontocerebellar hypoplasia in extreme prematurity: clinical and neuroimaging findings
DI Zafeiriou, A Ververi, A Anastasiou, V Soubasi, E Vargiami
Pediatric Neurology 48 (1), 48-51, 2013
112013
Flash VEP findings in children with bilateral spastic cerebral palsy: Correlation with clinico-radiological parameters
E Vargiami, DI Zafeiriou, N Kozeis, A Ververi, E Kontopoulos, ...
Journal of Pediatric Neurology 6 (4), 329-339, 2008
72008
Multiple coronary artery microfistulas in a girl with Kleefstra syndrome
E Vargiami, A Ververi, H Al-Mutawa, G Gioula, S Gerou, F Rouvalis, ...
Case Reports in Genetics 2016 (1), 3056053, 2016
52016
Life-threatening hyponatremia and acute renal failure due to iatrogenic neonatal bladder rupture
N Printza, A Ververi, M Bandouraki, E Vargiami, D Gidaris, F Papachristou
Urologia Internationalis 88 (2), 238-240, 2012
52012
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
A Ververi, S Zagaglia, L Menzies, J Baptista, R Caswell, S Baulac, ...
Human Molecular Genetics 32 (4), 580-594, 2023
42023
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