ABCB1 Polymorphisms and Drug-Resistant Epilepsy in a Tunisian Population
Hila, Lamia, Ben Youssef Turki, Ilhem, Klaa, Hedia, Chouchi, Malek
Published in Disease markers (2019)
Published in Disease markers (2019)
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Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood
Rebai, Ibtihel, Ben Rhouma, Hanene, Kraoua, Ichraf, Klaa, Hedia, Rouissi, Aida, Ben Youssef-Turki, Ilhem, Gouider-Khouja, Neziha
Published in Brain & development (Tokyo. 1979) (01.01.2015)
Published in Brain & development (Tokyo. 1979) (01.01.2015)
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Relationship between ABCB1 3435TT genotype and antiepileptic drugs resistance in Epilepsy: updated systematic review and meta-analysis
Chouchi, Malek, Kaabachi, Wajih, Klaa, Hedia, Tizaoui, Kalthoum, Turki, Ilhem Ben-Youssef, Hila, Lamia
Published in BMC neurology (15.02.2017)
Published in BMC neurology (15.02.2017)
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Neuronal ceroïd‐lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series
Ben Younes, Thouraya, Kraoua, Ichraf, Snanoudj, Sarah, Klaa, Hedia, Benrhouma, Hanene, Rouissi, Aida, Caillaud, Catherine, Chaabouni, Myriam, Miladi, Najoua, Bekri, Soumeya, Ben Youssef‐Turki, Ilhem
Published in Clinical genetics (01.08.2022)
Published in Clinical genetics (01.08.2022)
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Turki Ben Youssef, Ilhem, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha
Published in PloS one (06.10.2021)
Published in PloS one (06.10.2021)
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Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families
Kraoua, Ichraf, Jamoussi, Maha, Drissi, Cyrine, Kraoua, Lilia, Drunat, Séverine, Benrhouma, Hanene, Ben Younes, Thouraya, Nagi, Sonia, Abdelhak, Sonia, Boespflug Tanguy, Odile, Youssef‐Turki, Ilhem Ben, Trabelsi, Mediha, Dorboz, Imen
Published in Molecular genetics & genomic medicine (01.10.2024)
Published in Molecular genetics & genomic medicine (01.10.2024)
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Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology
Lahbib, Saida, Leblond, Claire S., Hamza, Mariem, Regnault, Béatrice, Lemée, Laure, Mathieu, Alexandre, Jaouadi, Hager, Mkaouar, Rahma, Youssef-Turki, Ilhem Ben, Belhadj, Ahlem, Kraoua, Ichraf, Bourgeron, Thomas, Abdelhak, Sonia
Published in Journal of applied genetics (07.02.2019)
Published in Journal of applied genetics (07.02.2019)
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Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia
Ben Achour, Nedia, Mrabet, Saloua, Rebai, Ibtihel, Abid, Ines, Benrhouma, Hanene, Klaa, Hedia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef Turki, Ilhem
Published in Brain & development (Tokyo. 1979) (01.10.2017)
Published in Brain & development (Tokyo. 1979) (01.10.2017)
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Journal Article
Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review
Ben Youssef-Turki, Ilhem, Rouissi, Aida, Nagi, Sonia, Benrhouma, Hanene, Ben Younes, Thouraya, Klaa, Hedia, Kraoua, Ichraf
Published in Case reports in neurological medicine (24.06.2020)
Published in Case reports in neurological medicine (24.06.2020)
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Journal Article
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity
Maroofian, Reza, Sarraf, Payam, O'Brien, Thomas J, Kamel, Mona, Cakar, Arman, Elkhateeb, Nour, Lau, Tracy, Patil, Siddaramappa Jagdish, Record, Christopher J, Horga, Alejandro, Essid, Miriam, Selim, Laila, Benrhouma, Hanene, Ben Younes, Thouraya, Zifarelli, Giovanni, Pagnamenta, Alistair T, Bauer, Peter, Khundadze, Mukhran, Mirecki, Andrea, Kamel, Sara Mahmoud, Elmonem, Mohamed A, Ghayoor Karimiani, Ehsan, Jamshidi, Yalda, Offiah, Amaka C, Rossor, Alexander M, Youssef-Turki, Ilhem Ben, Hübner, Christian A, Munot, Pinki, Reilly, Mary M, Brown, André E X, Nagy, Sara, Houlden, Henry
Published in Brain (London, England : 1878) (05.07.2024)
Published in Brain (London, England : 1878) (05.07.2024)
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Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review
Ben Achour, Nedia, Ben Younes, Thouraya, Rebai, Ibtihel, Ben Ahmed, Melika, Kraoua, Ichraf, Ben Youssef–Turki, Ilhem
Published in European journal of paediatric neurology (01.05.2018)
Published in European journal of paediatric neurology (01.05.2018)
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Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
Ververi, Athina, Zagaglia, Sara, Menzies, Lara, Baptista, Julia, Caswell, Richard, Baulac, Stephanie, Ellard, Sian, Lynch, Sally, Jacques, Thomas S, Chawla, Maninder Singh, Heier, Martin, Kulseth, Mari Ann, Mero, Inger-Lise, Våtevik, Anne Katrine, Kraoua, Ichraf, Ben Rhouma, Hanene, Ben Younes, Thouraya, Miladi, Zouhour, Ben Youssef Turki, Ilhem, Jones, Wendy D, Clement, Emma, Eltze, Christin, Mankad, Kshitij, Merve, Ashirwad, Parker, Jennifer, Hoskins, Bethan, Pressler, Ronit, Sudhakar, Sniya, DeVile, Catherine, Homfray, Tessa, Kaliakatsos, Marios, Robinson, Robert, Keim, Sara Margrete Bøen, Habibi, Imen, Reymond, Alexandre, Sisodiya, Sanjay M, Hurst, Jane A
Published in Human molecular genetics (27.01.2023)
Published in Human molecular genetics (27.01.2023)
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Next-generation sequencing of Tunisian Leigh syndrome patients reveals novel variations: impact for diagnosis and treatment
Hechmi, Meriem, Charif, Majida, Kraoua, Ichraf, Fassatoui, Meriem, Dallali, Hamza, Desquiret-Dumas, Valerie, Bris, Céline, Goudenège, David, Drissi, Cyrine, Galaï, Saïd, Ouerhani, Slah, Procaccio, Vincent, Amati-Bonneau, Patrizia, Abdelhak, Sonia, Ben Youssef-Turki, Ilhem, Lenaers, Guy, Kefi, Rym
Published in Bioscience reports (01.09.2022)
Published in Bioscience reports (01.09.2022)
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Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
Gouiza, Ismail, Hechmi, Meriem, Zioudi, Abir, Dallali, Hamza, Kheriji, Nadia, Charif, Majida, Le Mao, Morgane, Galai, Said, Kraoua, Lilia, Ben Youssef-Turki, Ilhem, Kraoua, Ichraf, Lenaers, Guy, Kefi, Rym
Published in Frontiers in genetics (12.01.2024)
Published in Frontiers in genetics (12.01.2024)
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Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort
Douma, Bissene, Ben Younes, Thouraya, Benrhouma, Hanene, Miladi, Zouhour, Zamali, Imen, Rouissi, Aida, Klaa, Hedia, Kraoua, Ichraf, Ben Ahmed, Melika, Ben Youssef Turki, Ilhem
Published in Journal of Immunology Research (2021)
Published in Journal of Immunology Research (2021)
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Journal Article
Early Life Epilepsy and Episodic Apnea Revealing an ATP1A3 Mutation: Report of a Pediatric Case and Literature Review
Younes, Thouraya Ben, Benrhouma, Hanene, Klaa, Hedia, Rouissi, Aida, Chaabouni, Myriam, Kraoua, Ichraf, Youssef-Turki, Ilhem Ben
Published in Neuropediatrics (01.10.2018)
Published in Neuropediatrics (01.10.2018)
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Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years
Ben Youssef Turki, Ilhem, Rouissi, Aida, Klaa, Hedia, Benrhouma, Hanene, Raddadi, Sarra, Rebai, Ibtihel, Ben Achour, Nedia, Kraoua, Ichraf
Published in BioMed research international (01.01.2017)
Published in BioMed research international (01.01.2017)
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Journal Article
Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review
Mrabet, Saloua, Ben Achour, Nedia, Kraoua, Ichraf, Benrhouma, Hanène, Klaa, Hedia, Rouissi, Aida, Ben Ahmed, Malika, Ben Youssef Turki, Ilhem
Published in European journal of paediatric neurology (01.11.2015)
Published in European journal of paediatric neurology (01.11.2015)
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