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Ververi, Athina
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Online (35)
Mediatypes
Articles (Online) (18)
OpenAccess-fulltext (17)
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1
X-linked hypophosphatemia due to a de novo novel splice-sit..:
Fourikou, Maria
;
Karipiadou, Aristea
;
Ververi, Athina
...
Bone Reports. 20 (2024) - p. 101731 , 2024
Link:
https://doi.org/10.1016/..
?
2
The Effect of Maternal Diet and Physical Activity on the Ep..:
Panagiotidou, Anastasia
;
Chatzakis, Christos
;
Ververi, Athina
..
Genes. 15 (2024) 1 - p. 76 , 2024
Link:
https://doi.org/10.3390/..
?
3
A novel ABCC9 variant in a Greek family with Cantu syndrome..:
Gao, Jian
;
Ververi, Athina
;
Thompson, Ellen
...
American Journal of Medical Genetics Part A. , 2024
Link:
https://doi.org/10.1002/..
?
4
Bowel Perforation in Vascular Ehlers–Danlos Syndrome: Case ..:
Menni, Alexandra
;
Tzikos, Georgios
;
Sarafis, Alexandros
...
Journal of Personalized Medicine. 13 (2023) 8 - p. 1247 , 2023
Link:
https://doi.org/10.3390/..
?
5
Beckwith–Wiedemann syndrome with multiple hepatic and cutan..:
Moutafi, Maria
;
Gkiourtzis, Nikolaos
;
Ververi, Athina
...
American Journal of Medical Genetics Part A. 194 (2023) 1 - p. 88-93 , 2023
Link:
https://doi.org/10.1002/..
?
6
Lethal COG6‐CDG in neonatal patient with arachnodactyly, jo..:
Ververi, Athina
;
Stathopoulou, Theodora
;
Kontou, Aggeliki
...
Pediatric Dermatology. 39 (2022) 2 - p. 314-315 , 2022
Link:
https://doi.org/10.1111/..
?
7
Expanding the phenotype of TAB2 variants and literature rev..:
Woods, Emily
;
Marson, Imogen
;
Coci, Emanuele
...
American Journal of Medical Genetics Part A. 188 (2022) 11 - p. 3331-3342 , 2022
Link:
https://doi.org/10.1002/..
?
8
Germline homozygous missense DEPDC5 variants cause severe r..:
Ververi, Athina
;
Zagaglia, Sara
;
Menzies, Lara
...
Human Molecular Genetics. 32 (2022) 4 - p. 580-594 , 2022
Link:
https://doi.org/10.1093/..
?
9
Patient with recurrent mosaicKRASvariant: Rare oculoectoder..:
Ververi, Athina
;
Laidou, Stamatia
;
Chatzidimitriou, Anastasia
...
The Journal of Dermatology. 49 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1111/..
?
10
KIF1A‐related disorders in children: A wide spectrum of cen..:
Nemani, Tarishi
;
Steel, Dora
;
Kaliakatsos, Marios
...
Journal of the Peripheral Nervous System. 25 (2020) 2 - p. 117-124 , 2020
Link:
https://doi.org/10.1111/..
?
11
Novel truncating mutations in CTNND1 cause a dominant crani..:
Alharatani, Reham
;
Ververi, Athina
;
Beleza-Meireles, Ana
...
Human Molecular Genetics. 29 (2020) 11 - p. 1900-1921 , 2020
Link:
https://doi.org/10.1093/..
?
12
Multiple Coronary Artery Microfistulas in a Girl with Kleef..:
Vargiami, Euthymia
;
Ververi, Athina
;
Al-Mutawa, Hamda
...
Case Reports in Genetics. 2016 (2016) - p. 1-5 , 2016
Link:
https://doi.org/10.1155/..
?
13
Autism spectrum disorders: The quest for genetic syndromes:
Zafeiriou, Dimitrios I.
;
Ververi, Athina
;
Dafoulis, Vaios
..
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 162 (2013) 4 - p. 327-366 , 2013
Link:
https://doi.org/10.1002/..
?
14
Pontocerebellar Hypoplasia in Extreme Prematurity: Clinical..:
Zafeiriou, Dimitrios I.
;
Ververi, Athina
;
Anastasiou, Athanasia
..
Pediatric Neurology. 48 (2013) 1 - p. 48-51 , 2013
Link:
https://doi.org/10.1016/..
?
15
Severe clinical presentation in monozygotic twins with 10p1..:
Vargiami, Euthymia
;
Ververi, Athina
;
Kyriazi, Maria
...
American Journal of Medical Genetics Part A. 164 (2013) 3 - p. 764-768 , 2013
Link:
https://doi.org/10.1002/..
1-15