Methylmalonic acidemia and hyperglycemia: An unusual association
Imen, Marouani, Hanene, Benrhouma, Ichraf, Kraoua, Aida, Rouissi, Ilhem, Turki, Naziha, Kaabachi, Neziha, Gouider-Khouja
Published in Brain & development (Tokyo. 1979) (01.02.2012)
Published in Brain & development (Tokyo. 1979) (01.02.2012)
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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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Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
Ishihara, Lianna, Gibson, Rachel A., Warren, Liling, Amouri, Rim, Lyons, Kelly, Wielinski, Catherine, Hunter, Christine, Swartz, Jina E., Elango, Ramu, Akkari, P. Anthony, Leppert, David, Surh, Linda, Reeves, Kevin H., Thomas, Siwan, Ragone, Leigh, Hattori, Nobutaka, Pahwa, Rajesh, Jankovic, Joseph, Nance, Martha, Freeman, Alan, Gouider-Khouja, Neziha, Kefi, Mounir, Zouari, Mourad, Ben Sassi, Samia, Ben Yahmed, Samia, El Euch-Fayeche, Ghada, Middleton, Lefkos, Burn, David J., Watts, Ray L., Hentati, Faycal
Published in Movement disorders (01.01.2007)
Published in Movement disorders (01.01.2007)
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Eye movements in parkinsonian syndromes
Vidailhet, M, Rivaud, S, Gouider-Khouja, N, Pillon, B, Bonnet, A M, Gaymard, B, Agid, Y, Pierrot-Deseilligny, C
Published in Annals of neurology (01.04.1994)
Published in Annals of neurology (01.04.1994)
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Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review
Khadija, Bochra, Rjiba, Khouloud, Dimassi, Sarra, Dahleb, Wafa, Kammoun, Molka, Hannechi, Hanen, Miladi, Najoua, Gouider-khouja, Neziha, Saad, Ali, Mougou-Zerelli, Soumaya
Published in Molecular cytogenetics (03.10.2022)
Published in Molecular cytogenetics (03.10.2022)
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Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
Tomiyama, Hiroyuki, Li, Yuanzhe, Funayama, Manabu, Hasegawa, Kazuko, Yoshino, Hiroyo, Kubo, Shin-Ichiro, Sato, Kenichi, Hattori, Tatsuya, Lu, Chin-Song, Inzelberg, Rivka, Djaldetti, Ruth, Melamed, Eldad, Amouri, Rim, Gouider-Khouja, Neziha, Hentati, Faycal, Hatano, Yasuko, Wang, Mei, Imamichi, Yoko, Mizoguchi, Koichi, Miyajima, Hiroaki, Obata, Fumiya, Toda, Tatsushi, Farrer, Matthew J., Mizuno, Yoshikuni, Hattori, Nobutaka
Published in Movement disorders (01.08.2006)
Published in Movement disorders (01.08.2006)
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Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
Gouider-Khouja, Neziha, Larnaout, Abdelmajid, Amouri, Rim, Sfar, Sana, Belal, Samir, Ben Hamida, Christiane, Ben Hamida, Mongi, Hattori, Nobutaka, Mizuno, Yoshikuni, Hentati, Fayçal
Published in Parkinsonism & related disorders (01.06.2003)
Published in Parkinsonism & related disorders (01.06.2003)
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Association of Amyotrophic Lateral Sclerosis and Dopa-responsive dystonia in a Tunisian patient
KACEM, Imen, SGHAIER, Ikram, BEN RHOUMA, Hanene, RATTI, Antonia, TICOZZI, Nicola, Silani, V.I.N.C.E.N.Z.O., GOUIDER-KHOUJA, Neziha, GOUIDER, Riadh
Published in Parkinsonism & related disorders (01.10.2024)
Published in Parkinsonism & related disorders (01.10.2024)
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Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries
Tomiyama, Hiroyuki, Li, Yuanzhe, Funayama, Manabu, Hasegawa, Kazuko, Yoshino, Hiroyo, Kubo, Shin-Ichiro, Sato, Kenichi, Hattori, Tatsuya, Lu, Chin-Song, Inzelberg, Rivka, Djaldetti, Ruth, Melamed, Eldad, Amouri, Rim, Gouider-Khouja, Neziha, Hentati, Faycal, Hatano, Yasuko, Wang, Mei, Imamichi, Yoko, Mizoguchi, Koichi, Miyajima, Hiroaki, Obata, Fumiya, Toda, Tatsushi, Farrer, Matthew J., Mizuno, Yoshikuni, Hattori, Nobutaka
Published in Movement disorders (01.08.2006)
Published in Movement disorders (01.08.2006)
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DigiPark Application: Collecting Feedback from Both Neurologists and Patients to Guide Development (Preprint)
Duracinsky, Martin, Brown Hajdukova, Eva, Peretz, Fabienne, Sauzin, Julie, Gouider-Khouja, Neziha, Atlani, Caroline, Dalili, Djamchid
Published in JMIR human factors (30.11.2023)
Published in JMIR human factors (30.11.2023)
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"Pure" striatonigral degeneration and Parkinson's disease: a comparative clinical study
Gouider-Khouja, N, Vidailhet, M, Bonnet, A M, Pichon, J, Agid, Y
Published in Movement disorders (01.05.1995)
Published in Movement disorders (01.05.1995)
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First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation
Ghorbel, Rania, Ghorbel, Raouia, Rouissi, Aida, Fendri-Kriaa, Nourhene, Ben Salah, Ghada, Belguith, Neila, Ammar-Keskes, Leila, Gouider-Khouja, Neziha, Fakhfakh, Faiza
Published in Biochemical and biophysical research communications (26.02.2018)
Published in Biochemical and biophysical research communications (26.02.2018)
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Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome
Romani, Marta, Micalizzi, Alessia, Kraoua, Ichraf, Dotti, Maria Teresa, Cavallin, Mara, Sztriha, László, Ruta, Rosario, Mancini, Francesca, Mazza, Tommaso, Castellana, Stefano, Hanene, Benrhouma, Carluccio, Maria Alessandra, Darra, Francesca, Máté, Adrienn, Zimmermann, Alíz, Gouider-Khouja, Neziha, Valente, Enza Maria
Published in Orphanet journal of rare diseases (05.05.2014)
Published in Orphanet journal of rare diseases (05.05.2014)
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Évaluation par les neurologues et les patients de DigiPark, une application dédiée à la télésurveillance (TS) de la maladie de Parkinson (MP)
Duracinsky, Martin, Hajdukova, Eva Brown, Péretz, Fabienne, Sauzin, Julie, Gouider-Khouja, Neziha, Atlani, Caroline, Dalili, Djamchid
Published in Revue neurologique (01.04.2024)
Published in Revue neurologique (01.04.2024)
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Movement disorders in neuro-metabolic diseases
Gouider-Khouja, Neziha, Kraoua, Ichraf, Benrhouma, Hanene, Fraj, Narjes, Rouissi, Aida
Published in European journal of paediatric neurology (01.07.2010)
Published in European journal of paediatric neurology (01.07.2010)
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Status dystonicus in childhood
Touati, Nahla, Ben Rhouma, Hanène, Kraoua, Ichraf, Klaa, Hédia, Turki, Ilhem, Gouider-Khouja, Neziha
Published in Tunisie Medicale (01.12.2015)
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Published in Tunisie Medicale (01.12.2015)
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