N. Gouider-Khouja

发表

Y. Agid, A. Bonnet, M. Vidailhet, 1994, Annals of neurology.

[Treatment of cervical dystonia with botulinum toxin].

N. Gouider-Khouja, I. Turki, M. Ben Hamida, 1999, La Tunisie medicale.

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

T. Mazza, S. Castellana, E. Valente, 2014, Orphanet Journal of Rare Diseases.

Epilepsy Aspects and EEG Patterns in Neuro-Metabolic Diseases

N. Gouider-Khouja, H. Benrhouma, A. Rouissi, 2011 .

Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome.

N. Gouider-Khouja, F. Hentati, N. Miladi, 2002, Parkinsonism & related disorders.

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

N. Gouider-Khouja, H. Klaa, A. Rouissi, 2015, Brain and Development.

Movement disorders in neuro-metabolic diseases.

N. Gouider-Khouja, H. Benrhouma, A. Rouissi, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Wilson's disease.

N. Gouider-Khouja, 2009, Parkinsonism & related disorders.

Aicardi-Goutières syndrome: A cause of CSF chronic hyperlymphocytosis

N. Gouider-Khouja, I. Turki, I. Kraoua, 2010, Journal of Pediatric Neurology.

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

A. Saâd, N. Gouider-Khouja, S. Dimassi, 2022, Molecular Cytogenetics.

Do parkinsonian symptoms and levodopa‐induced dyskinesias start in the foot?

Y. Agid, R. Marconi, A. Bonnet, 1994, Neurology.

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.

F. Fakhfakh, N. Gouider-Khouja, Ghada Ben Salah, 2018, Biochemical and biophysical research communications.

3-Phosphoglycerate Dehydrogenase Deficiency: Description of Two New Cases in Tunisia and Review of the Literature

E. Schaftingen, G. Briand, N. Gouider-Khouja, 2013, Neuropediatrics.

[Post-herpes simplex encephalitis chorea: Viral replication or immunological mechanism?].

N. Gouider-Khouja, I. Turki, H. Benrhouma, 2015, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

J. Jankovic, K. Lyons, R. Pahwa, 2007, Movement disorders : official journal of the Movement Disorder Society.

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries

M. Farrer, N. Hattori, R. Djaldetti, 2006, Movement disorders : official journal of the Movement Disorder Society.

Clinical and genetic study of familial Parkinson’s disease in Tunisia

M. Hamida, N. Gouider-Khouja, F. Hentati, 2000, Neurology.

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency

M. Hamida, N. Gouider-Khouja, I. Turki, 2001, European journal of neurology.

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3

M. Hamida, N. Gouider-Khouja, F. Hentati, 2000, Neuromuscular Disorders.

[Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension].

N. Gouider-Khouja, H. Jemel, H. Benrhouma, 2013, Neuro-Chirurgie.

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

E. Génin, H. Lochmüller, J. Pouget, 2008, Neurology.

congenital myasthenia in North Africa 1293 insG founder mutation is a frequent cause of CHRNE The

E. Génin, J. Pouget, A. Barois, 2008 .

Joubert syndrome and related disorders: Report of five Tunisian cases

N. Gouider-Khouja, M. Hamouda, A. Rouissi, 2010, Journal of Pediatric Neurology.

Infantile and childhood onset PLA2G6‐associated neurodegeneration in a large North African cohort

C. Drissi, T. Mazza, S. Castellana, 2015, European journal of neurology.

[Botulinum toxin in the management of spasticity in children].

N. Gouider-Khouja, H. Benrhouma, H. Klaa, 2014, Revue neurologique.

Eye Movements in Pmhnsonian Syndromes

Y. Agid, A. Bonnet, M. Vidailhet, 1994 .

Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy.

Y. Agid, M. Vidailhet, B. Dubois, 1995, Journal of neurology, neurosurgery, and psychiatry.

degeneration: comparison with Parkinson's disease and progressive supranuclear palsy

Y. Agid, M. Vidailhet, B. Dubois, 2022 .

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.

N. Hattori, Y. Mizuno, M. Ben Hamida, 2003, Parkinsonism & related disorders.

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review

C. Drissi, O. Boespflug-Tanguy, S. Abdelhak, 2021, Neuropediatrics.

“Pure” striatonigral degeneration and Parkinson's disease: A comparative clinical study

Y. Agid, A. Bonnet, M. Vidailhet, 1995, Movement disorders : official journal of the Movement Disorder Society.

patternofstriatonigral degeneration: comparison withParkinson's disease andprogressive supranuclear palsy

B. Pillon, B. Deweer, N. Gouider-Khouja, 1995 .

[A comparative study of clinical and paramedical aspects of multiple sclerosis in Tunisia].

N. Gouider-Khouja, F. Hentati, N. Ammar, 2006, Revue neurologique.

Saccades and antisaccades in parkinsonian syndromes.

C. Kennard, Y. Agid, M. Vidailhet, 1999, Advances in neurology.

Arabic adaptation of Phonology and Memory test using entropy-based analysis of word complexity

Raja Ghozi, Meriem Jaïdane, Neziha Gouider-Khouja, 2012, 2012 11th International Conference on Information Science, Signal Processing and their Applications (ISSPA).

Anti-NMDA receptor encephalitis mimicking a primary psychiatric disorder in a 13-year-old girl.

F. Ducray, N. Gouider-Khouja, A. Didelot, 2013, Turk psikiyatri dergisi = Turkish journal of psychiatry.

Mirror Movements and Myelomeningocele: Report of A Single Case and Review of Literature

C. Drissi, N. Gouider-Khouja, H. Benrhouma, 2013, Iranian journal of child neurology.

Seronegative myasthenia gravis with bladder dysfunction.

I. Marouani, N. Gouider-Khouja, I. Turki, 2012, Revue neurologique (Paris).

Cognitive and psychological profile in Tunisian children with Duchenne muscular dystrophy

N. Gouider-Khouja, H. Benrhouma, H. Klaa, 2013, Journal of the Neurological Sciences.

[Botulinum toxin in the management of spasticity in children].

N. Gouider-Khouja, H. Benrhouma, H. Klaa, 2014, Revue neurologique.

Movement disorders in neuro-metabolic diseases.

N. Gouider-Khouja, H. Benrhouma, A. Rouissi, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.