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Fendri-Kriaa, Nourhène
15
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1
First report of an unusual novel double mutation affecting ..:
Ghorbel, Rania
;
Ghorbel, Raouia
;
Rouissi, Aida
...
Biochemical and Biophysical Research Communications. 497 (2018) 1 - p. 93-101 , 2018
Link:
https://doi.org/10.1016/..
?
2
Clinical, Molecular, and Computational Analysis in Patients..:
Kharrat, Marwa
;
Kamoun, Yosra
;
Kamoun, Fatma
...
Journal of Child Neurology. 32 (2017) 8 - p. 694-703 , 2017
Link:
https://doi.org/10.1177/..
?
3
Phenotypic variability in two infants sharing the same MECP..:
Kharrat, Marwa
;
Hsairi, Ines
;
Doukali, Hajer
...
Acta Neurologica Belgica. 117 (2016) 1 - p. 251-258 , 2016
Link:
https://doi.org/10.1007/..
?
4
A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG–..:
Kharrat, Marwa
;
Hsairi, Ines
;
Fendri-Kriaa, Nourhene
...
Journal of Child Neurology. 30 (2015) 13 - p. 1715-1721 , 2015
Link:
https://doi.org/10.1177/..
?
5
An interethnic variability and a functional prediction of D..:
Ben Salah, Ghada
;
Fendri-Kriaa, Nourhene
;
Kamoun, Hassen
...
Molecular Biology Reports. 39 (2012) 10 - p. 9639-9647 , 2012
Link:
https://doi.org/10.1007/..
?
6
Novel double deletions in the MECP2 gene in Tunisian Rett p..:
Fendri-Kriaa, Nourhene
;
Rouissi, Aida
;
Ghorbel, Rania
...
Gene. 502 (2012) 2 - p. 163-167 , 2012
Link:
https://doi.org/10.1016/..
?
7
A putative disease-associated haplotype within the SCN1A ge..:
Fendri-Kriaa, Nourhène
;
Boujilbene, Salma
;
Kammoun, Fatma
...
Biochemical and Biophysical Research Communications. 408 (2011) 4 - p. 654-657 , 2011
Link:
https://doi.org/10.1016/..
?
8
Novel Mutations in the C-Terminal Region of the MECP2 Gene ..:
Fendri-Kriaa, Nourhene
;
Rouissi, Aida
;
Ghorbel, Rania
...
Journal of Child Neurology. 27 (2011) 5 - p. 564-568 , 2011
Link:
https://doi.org/10.1177/..
?
9
A case of a Tunisian Rett patient with a novel double-mutat..:
Fendri-Kriaa, Nourhene
;
Hsairi, Ines
;
Kifagi, Chamseddine
...
Biochemical and Biophysical Research Communications. 409 (2011) 2 - p. 270-274 , 2011
Link:
https://doi.org/10.1016/..
?
10
A novel m.3395A>G missense mutation in the mitochondrial ND..:
Chamkha, Imen
;
Mkaouar-Rebai, Emna
;
Aloulou, Hajer
...
Biochemical and Biophysical Research Communications. 404 (2011) 1 - p. 504-510 , 2011
Link:
https://doi.org/10.1016/..
?
11
Mutational Analysis of the MECP2 Gene in Tunisian Patients ..:
Fendri-Kriaa, Nourhene
;
Mkaouar-Rebai, Emna
;
Moalla, Dorsaf
...
Journal of Child Neurology. 25 (2010) 8 - p. 1042-1046 , 2010
Link:
https://doi.org/10.1177/..
?
12
The First Genome-Wide Scan in a Tunisian Family With Genera..:
Fendri-Kriaa, Nourhene
;
Louhichi, Nacim
;
Mkaouar-Rebai, Emna
...
Journal of Child Neurology. 25 (2010) 11 - p. 1362-1368 , 2010
Link:
https://doi.org/10.1177/..
?
13
Congenital factor XIII deficiency caused by two mutations i..:
Louhichi, Nacim
;
Medhaffar, Moez
;
HadjSalem, Ikhlass
...
Annals of Hematology. 89 (2009) 5 - p. 499-504 , 2009
Link:
https://doi.org/10.1007/..
?
14
Association between Leptin gene polymorphisms and plasma le..:
Fourati, Mouna
;
Mnif, Mouna
;
Kharrat, Najla
...
Gene. 527 (2013) 1 - p. 75-81 , 2013
Link:
https://doi.org/10.1016/..
?
15
A case of Kearns–Sayre syndrome with two novel deletions (9..:
Mkaouar-Rebai, Emna
;
Chamkha, Imen
;
Kammoun, Thouraya
...
Mitochondrion. 10 (2010) 5 - p. 449-455 , 2010
Link:
https://doi.org/10.1016/..
1-15