SQSTM1 mutation: Description of the first Tunisian case and literature review von Akkari, M., Kraoua, I., Klaa, H., Benrhouma, H., Ben Younes, T., Rouissi, A., Chaabouni, M., Ben Youssef‐Turki, I.

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Comment on ‘Acute flaccid myelitis in childhood: a retrospective cohort study’ von Ben Achour, N., Jeridi, C., Rebai, I., Nagi, S., Kraoua, I., Ben Youssef –Turki, I.

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Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration von Kraoua, I., Romani, M., Tonduti, D., BenRhouma, H., Zorzi, G., Zibordi, F., Ardissone, A., Gouider-Khouja, N., Ben Youssef-Turki, I., Nardocci, N., Valente, E. M.

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Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients von Jouini, L., Sahli, C. A., Laaouini, N., Ouali, F., Youssef, I. Ben, Dakhlaoui, B., Othmeni, R., Ouennich, F., Fredj, S. Hadj, Siala, H., Becher, M., Toumi, N. E., Fattoum, S., Hafsia, R., Bibi, A., Messaoud, T.

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Acquired demyelinating syndromes of the central nervous system in children: study of a cohort of 47 cases von Ben Achour, N, Raddadi, S, Benrhouma, H, Klaa, H, Rouissi, A, Kraoua, I, Ben Youssef Turki, I

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Atypical presentations of Guillain-Barré Syndrome in children von El Mabrouk, E, Ben Achour, N, Turki, A, Benrhouma, H, Klaa, H, Kraoua, I, Ben Youssef-Turki, I

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Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child von Ben Younes, T., Kraoua, I., Benrhouma, H., Nasrallah, F., Ben Achour, N., Klaa, H., Hassen-Rouissi, A., Drissi, C., Benoist, J.-F., Ben Youssef-Turki, I.

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Acute disseminated encephalomyelitis in Tunisia: Report of a pediatric cohort von Ben Achour, N, Ben Waddey, O, Kraoua, I, Benrhouma, H, Klaa, H, Rouissi, A, Ben Youssef-Turki, I

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Botulinum toxin in the management of spasticity in children von Benrhouma, H, Yacoubi, J, Kraoua, I, Klaa, H, Ben Youssef-Turki, I, Gouider-Khouja, N

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Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension von Ben Achour, N, Kraoua, I, Rouissi, A, Benrhouma, H, Ben Youssef-Turki, I, Jemel, H, Gouider-Khouja, N

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RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity von Maroofian, R, Sarraf, P, O'Brien, TJ, Kamel, M, Cakar, A, Elkhateeb, N, Lau, T, Patil, SJ, Record, CJ, Horga, A, Essid, M, Selim, L, Benrhouma, H, Ben Younes, T, Zifarelli, G, Pagnamenta, AT, Bauer, P, Khundadze, M, Mirecki, A, Kamel, SM, Elmonem, MA, Karimiani, EG, Jamshidi, Y, Offiah, AC, Rossor, AM, Ben Youssef-Turki, I, Huebner, CA, Munot, P, Reilly, MM, Brown, AEX, Nagy, S, Houlden, H

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Type I glutaric aciduria: an unrecognized cause of progressive dystonia von Gouider-Khouja, N, Ben Youssef-Turki, I

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An overview of neurometabolic diseases in Tunisia. a 3-year prospective study von Kraoua, I, Benrhouma, H, Rouissi, A, Youssef-Turki, I Ben, Zouari, B, Kaabachi, N, Gouider-Khouja, N

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Centrifugation, Storage, and Filtration of Olive Oil in an Oil Mill: Effect on the Quality and Content of Minority Compounds von Moya, Manuel, de Torres, Antonia, Alcalá, Sonia, Vidal, Alfonso M., Espínola, Francisco

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Association between clinical expression and molecular heterogeneity in [beta]-thalassemia Tunisian patients von Jouini, L, Sahli, C A, Laaouini, N, Ouali, F, Youssef, I Ben, Dakhlaoui, B, Othmeni, R, Ouennich, F, Fredj, S Hadj, Siala, H, Becher, M, Toumi, N E, Fattoum, S, Hafsia, R, Bibi, A, Messaoud, T

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Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA 2G6 ‐associated neurodegeneration von Kraoua, I., Romani, M., Tonduti, D., BenRhouma, H., Zorzi, G., Zibordi, F., Ardissone, A., Gouider‐Khouja, N., Ben Youssef‐Turki, I., Nardocci, N., Valente, E. M.

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Optical parameters extraction of zinc oxide thin films doped with manganese using an innovative technique based on the dragonfly algorithm and their correlation to the structural p... von Settara, K., Lekoui, F., Akkari, H., Garoudja, E., Amrani, R., Filali, W., Oussalah, S., Hassani, S.

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Cognitive and psychological profile in Tunisian children with Duchenne muscular dystrophy von Klaa, H, Kraoua, I, Benrhouma, H, Rouissi, A, Gouider-Khouja, N, Youssef-Turki, I. Ben

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Management of muscular dystrophies in Tunisian children von Kraoua, I, Benrhouma, H, Klaa, H, Rouissi, A, Gouider-Khouja, N, Youssef-Turki, I. Ben

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Pelizaeus Merzbacher like disease in Tunisian children: A severe phenotype von Rebai, I, Kraoua, I, Dorboz, I, Benrhouma, H, Klaa, H, Rouissi, A, Boesflug-Tanguy, O, Gouider-Khouja, N, Youssef-Turki, I. Ben

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