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Hsairi, Ines
18
results:
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english (13)
french (5)
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1
MRI features in 17 patients with l2 hydroxyglutaric aciduri:
Fourati, Héla
;
Ellouze, Emna
;
Ahmadi, Mourad
...
European Journal of Radiology Open. 3 (2016) - p. 245-250 , 2016
Link:
https://doi.org/10.1016/..
?
2
The effect of a motor skills training program in the improv..:
Farhat, Faiçal
;
Hsairi, Ines
;
Baati, Hamza
...
Human Movement Science. 46 (2016) - p. 10-22 , 2016
Link:
https://doi.org/10.1016/..
?
3
Aspects électroencéphalographiques atypiques dans l'épileps..:
Zouari, Hela
;
Ben Jemaa, Sana
;
Sakka, Salma
...
Neurophysiologie Clinique/Clinical Neurophysiology. 46 (2016) 3 - p. 233 , 2016
Link:
https://doi.org/10.1016/..
?
4
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/..
?
5
Assessment of physical fitness and exercise tolerance in ch..:
Farhat, Faiçal
;
Hsairi, Ines
;
Baiti, Hamza
...
Research in Developmental Disabilities. 45-46 (2015) - p. 210-219 , 2015
Link:
https://doi.org/10.1016/..
?
6
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/..
?
7
Assessment of cardiorespiratory and neuromotor fitness in c..:
Farhat, Faiçal
;
Masmoudi, Kaouthar
;
Cairney, John
...
Research in Developmental Disabilities. 35 (2014) 12 - p. 3554-3561 , 2014
Link:
https://doi.org/10.1016/..
?
8
Les leucodystrophies (LD) de l'enfant : une étude à propos ..:
Ellouz, Emna
;
Kammoun, Nadège
;
Hsairi, Ines
...
Revue Neurologique. 168 (2012) - p. A112 , 2012
Link:
https://doi.org/10.1016/..
?
9
Caractéristiques du syndrome de Lennox-Gastaut faisant suit..:
Jardak, Fedia
;
Hsairi, Ines
;
Chtourou, Emna
...
Revue Neurologique. 168 (2012) - p. A63 , 2012
Link:
https://doi.org/10.1016/..
?
10
Opsoclonus-myoclonus associé à une rubéole : caractéristiqu..:
Ayadi, Ines
;
Ellouz, Emna
;
Abid, Imen
...
Revue Neurologique. 168 (2012) - p. A129-A130 , 2012
Link:
https://doi.org/10.1016/..
?
11
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/..
?
12
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/..
?
13
CAPN3 mRNA processing alteration caused by splicing mutatio..:
Salem, Ikhlass Hadj
;
Hsairi, Ines
;
Mezghani, Najla
...
Journal of Human Genetics. 57 (2011) 2 - p. 92-100 , 2011
Link:
https://doi.org/10.1038/..
?
14
A De Novo Mutation in the Adenosine Triphosphatase (ATPase)..:
Mkaouar-Rebai, Emna
;
Kammoun, Fatma
;
Chamkha, Imen
...
Journal of Child Neurology. 25 (2010) 6 - p. 770-775 , 2010
Link:
https://doi.org/10.1177/..
?
15
Le syndrome des pointes ondes continues du sommeil et troub..:
Ayadi, Ines
;
Salma, Sakka
;
Elouze, Sahar
...
Revue Neurologique. 172 (2016) - p. A56 , 2016
Link:
https://doi.org/10.1016/..
1-15