E-LIB Suche - Ergebnisse für: Kallabi, Fakhri

1

Neurological Characteristics of Allgrove Syndrome: A Case S..:

Salah, Dhoha Ben ; Elleuch, Mouna ; Trimeche, Oumeyma...
Annals of Child Neurology. 32 (2024) 2 - p. 130-134 , 2024

2

Molecular mechanisms underlying the defects of two novel mu..:

Ben Rhouma, Bochra ; Kley, Manuel ; Kallabi, Fakhri...
The Journal of Steroid Biochemistry and Molecular Biology. 227 (2023) - p. 106235 , 2023

Link: https://doi.org/10.1016/..

3

Characterisation of the Paenarthrobacter nicotinovorans ATC..:

El-Sabeh, Amada ; Mlesnita, Andreea-Mihaela ; Munteanu, Iustin-Tiberius...
BMC Genomics. 24 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

4

Molecular and computational characterization of ABCB11 and ..:

Khabou, Boudour ; Kallabi, Fakhri ; Abdelaziz, Rim Ben...
Annals of Human Genetics. 88 (2023) 3 - p. 194-211 , 2023

Link: https://doi.org/10.1111/..

5

Complete Genome Sequences of Two Closely Related Paenarthro..:

El-Sabeh, Amada ; Honceriu, Iasmina ; Kallabi, Fakhri...
Microbiology Resource Announcements. 11 (2022) 6 - p. , 2022

Link: https://doi.org/10.1128/..

6

Novel cases of Tunisian patients with mutations in the gene..:

Ben Rhouma, Bochra ; Kallabi, Fakhri ; Mahfoudh, Nadia...
The Journal of Steroid Biochemistry and Molecular Biology. 165 (2017) - p. 86-94 , 2017

Link: https://doi.org/10.1016/..

7

Whole mitochondrial genome screening of a family with mater..:

Tabebi, Mouna ; Charfi, Nadia ; Kallabi, Fakhri...
Journal of Diabetes and its Complications. 31 (2017) 1 - p. 253-259 , 2017

Link: https://doi.org/10.1016/..

8

Clinical and Genetic Characterization of 26 Tunisian Patien..:

Kallabi, Fakhri ; Belghuith, Neila ; Aloulou, Hajer...
Archives of Medical Research. 47 (2016) 2 - p. 105-110 , 2016

Link: https://doi.org/10.1016/..

9

Phenotypic variability in a Tunisian family with X-linked a..:

Kallabi, Fakhri ; Ellouz, Emna ; Tabebi, Mouna...
Clinica Chimica Acta. 453 (2016) - p. 141-146 , 2016

Link: https://doi.org/10.1016/..

10

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mu..:

Tabebi, Mouna ; Mkaouar-Rebai, Emna ; Mnif, Mouna...
Biochemical and Biophysical Research Communications. 459 (2015) 3 - p. 353-360 , 2015

Link: https://doi.org/10.1016/..

11

Splicing defects in ABCD1 gene leading to both exon skippin..:

Kallabi, Fakhri ; Hadj Salem, Ikhlass ; Ben Chehida, Amel...
Neuroscience Research. 97 (2015) - p. 7-12 , 2015

Link: https://doi.org/10.1016/..

12

A novel frameshift mutation in BLM gene associated with hig..:

Ben Salah, Ghada ; Hadj Salem, Ikhlas ; Masmoudi, Abderrahmen...
Molecular Biology Reports. 41 (2014) 11 - p. 7373-7380 , 2014

Link: https://doi.org/10.1007/..

13

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/..

14

Polymorphisms of glutathione S-transferases M1, T1, P1 and ..:

Ben Salah, Ghada ; Kallabi, Fakhri ; Maatoug, Sirine...
Gene. 498 (2012) 2 - p. 317-322 , 2012

Link: https://doi.org/10.1016/..

15

Cytocompatibility, gene-expression profiling, apoptotic, me..:

Samira, Jebahi ; Hassane, Oudadesse ; Mongi, Saoudi...
Biotechnology Letters. 36 (2014) 12 - p. 2571-2579 , 2014

Link: https://doi.org/10.1007/..