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Fendri-Kriaa, Nourhène
15  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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