Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort
Romani, M., Kraoua, I., Micalizzi, A., Klaa, H., Benrhouma, H., Drissi, C., Turki, I., Castellana, S., Mazza, T., Valente, E. M., Gouider-Khouja, N.
Published in European journal of neurology (01.01.2015)
Published in European journal of neurology (01.01.2015)
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Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration
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.
Published in European journal of neurology (01.04.2016)
Published in European journal of neurology (01.04.2016)
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Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family
Messaoud, O., Ben Rekaya, M., Kefi, R., Chebel, S., Boughammoura‐Bouatay, A., Bel Hadj Ali, H., Gouider‐Khouja, N., Zili, J., Frih‐Ayed, M., Mokhtar, I., Abdelhak, S., Zghal, M.
Published in British journal of dermatology (1951) (01.04.2010)
Published in British journal of dermatology (1951) (01.04.2010)
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Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency
Gabsi, S., Gouider-Khouja, N., Belal, S., Fki, M., Kefi, M., Turki, I., Hamida, M. Ben, Kayden, H., Mebazaa, R., Hentati, F.
Published in European journal of neurology (01.09.2001)
Published in European journal of neurology (01.09.2001)
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Urinary disturbances in striatonigral degeneration and Parkinson's disease: clinical and urodynamic aspects
Bonnet, A M, Pichon, J, Vidailhet, M, Gouider-Khouja, N, Robain, G, Perrigot, M, Agid, Y
Published in Movement disorders (01.07.1997)
Published in Movement disorders (01.07.1997)
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Cognitive and psychological profile in Tunisian children with Duchenne muscular dystrophy
Klaa, H, Kraoua, I, Benrhouma, H, Rouissi, A, Gouider-Khouja, N, Youssef-Turki, I. Ben
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Management of muscular dystrophies in Tunisian children
Kraoua, I, Benrhouma, H, Klaa, H, Rouissi, A, Gouider-Khouja, N, Youssef-Turki, I. Ben
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Neurophysiological stud/INS;y in infantile neuroaxonal dystrophy: Retrospective review of seventeen North-African patients
Kraoua, I, Romani, M, Benrhouma, H, Klaa, H, Hassen-Rouissi, A, Valente, E.-M, Gouider-Khouja, N, Youssef-Turki, I. Ben
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Pelizaeus Merzbacher like disease in Tunisian children: A severe phenotype
Rebai, I, Kraoua, I, Dorboz, I, Benrhouma, H, Klaa, H, Rouissi, A, Boesflug-Tanguy, O, Gouider-Khouja, N, Youssef-Turki, I. Ben
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
Messaoud, O., Ben Rekaya, M., Ouragini, H., Benfadhel, S., Azaiez, H., Kefi, R., Gouider-Khouja, N., Mokhtar, I., Amouri, A., Boubaker, M. S., Zghal, M., Abdelhak, S.
Published in Archives of Dermatological Research (01.03.2012)
Published in Archives of Dermatological Research (01.03.2012)
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Brain imaging in chorea in Tunisian children
Nasri, A, Benrhouma, H, Rebai, I, Kraoua, I, Drissi, C, Klaa, H, Achour, N. Ben, Rouissi, A, Gouider-Khouja, N, Hammouda, M. Ben, Turki, I
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
Richard, P, Gaudon, K, Haddad, H, Ammar, A Ben, Genin, E, Bauché, S, Paturneau-Jouas, M, Müller, J S, Lochmüller, H, Grid, D, Hamri, A, Nouioua, S, Tazir, M, Mayer, M, Desnuelle, C, Barois, A, Chabrol, B, Pouget, J, Koenig, J, Gouider-Khouja, N, Hentati, F, Eymard, B, Hantaï, D
Published in Neurology (09.12.2008)
Published in Neurology (09.12.2008)
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Botulinum toxin in the management of spasticity in children
Benrhouma, H, Yacoubi, J, Kraoua, I, Klaa, H, Ben Youssef-Turki, I, Gouider-Khouja, N
Published in Revue neurologique (01.08.2014)
Published in Revue neurologique (01.08.2014)
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Clinical and therapeutic aspects in Tunisian patients with dystonia: a 5-year prospective study
Benrhouma, H, Kraoua, I, Klaa, H, Rouissi, A, Turki, I, Gouider-Khouja, N
Published in Revue neurologique (01.01.2013)
Published in Revue neurologique (01.01.2013)
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Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension
Ben Achour, N, Kraoua, I, Rouissi, A, Benrhouma, H, Ben Youssef-Turki, I, Jemel, H, Gouider-Khouja, N
Published in Neuro-chirurgie (01.04.2013)
Published in Neuro-chirurgie (01.04.2013)
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PO26-TH-04 Impact of a systematic protocol of management of progressive muscular dystrophy on disease parameters: a study of 45 cases over 5 years
Smirani, S, Gabsi-Gherairi, S, Fredj, N, Rouissi, A, Gouider-Khouja, N
Published in Journal of the neurological sciences (2009)
Published in Journal of the neurological sciences (2009)
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