E-LIB Suche - Ergebnisse für: Hsairi, Ines

1

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/..

2

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/..

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

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/..

5

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/..

6

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/..

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

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/..

9

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/..

10

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/..

11

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/..

12

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/..

13

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/..

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/..