Neziha Gouider-Khouja

Summary

Country: Tunisie

Publications

  1. ncbi request reprint Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome
    Neziha Gouider-Khouja
    Service de Neurologie, Institut National de Neurologie, La Rabta, Tunis 1007, Tunisia
    Parkinsonism Relat Disord 8:285-8. 2002
  2. ncbi request reprint [Type I glutaric aciduria: an unrecognized cause of progressive dystonia]
    N Gouider-Khouja
    Service de Neurologie Pediatrique, Institut National de Neurologie, Tunis, Tunisie
    Rev Neurol (Paris) 162:858-61. 2006
  3. ncbi request reprint Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
    Neziha Gouider-Khouja
    Service de Neurologie, Institut National de Neurologie, La Rabta, Tunis 1007, Tunisia
    Parkinsonism Relat Disord 9:247-51. 2003
  4. doi request reprint Movement disorders in neuro-metabolic diseases
    Neziha Gouider-Khouja
    Department of Child and Adolescent Neurology, Consultation of Movement Disorders and Botulinum Toxin, National Institute of Neurology, Tunis, Tunisia
    Eur J Paediatr Neurol 14:304-7. 2010
  5. doi request reprint Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child
    Ibtihel Rebai
    Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    Brain Dev 36:921-3. 2014
  6. doi request reprint 3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature
    Ichraf Kraoua
    Department of Child and Adolescent Neurology and UR 06 11, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    Neuropediatrics 44:281-5. 2013
  7. ncbi request reprint [Neurological complications of acute intermittent porphyria precipitated by porphyrinogenic drugs and efficiency of heme-arginate treatment]
    Rousanna Akopova-Larbi
    Service de Neurologie, Hopital Razi, Manouba, Tunis
    Tunis Med 87:621-6. 2009
  8. ncbi request reprint Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
    Hiroyuki Tomiyama
    Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan
    Mov Disord 21:1102-8. 2006
  9. ncbi request reprint Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
    Lianna Ishihara
    Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom
    Mov Disord 22:55-61. 2007

Collaborators

  • Rim Amouri
  • Emile van Schaftingen
  • Sana Sfar
  • Yoshikuni Mizuno
  • N Hattori
  • R Inzelberg
  • D J Burn
  • R Pahwa
  • Ruth Djaldetti
  • J Jankovic
  • Matthew James Farrer
  • Ichraf Kraoua
  • Ibtihel Rebai
  • Ilhem Turki
  • Aida Rouissi
  • Rousanna Akopova-Larbi
  • Lianna Ishihara
  • Faycal Hentati
  • Hiroyuki Tomiyama
  • Hanene Benrhouma
  • Irene Ceballos-Picot
  • Gilbert Briand
  • Habiba Chaabouni
  • Lilia Kraoua
  • Naziha Kaabachi
  • Elsa Wiame
  • Hanen Benrhouma
  • Fehmi Nasrallah
  • Riadh Gouider
  • Turki Ilhem Ben Youssef
  • Amina Gargouri
  • Siwan Thomas
  • Liling Warren
  • Jina E Swartz
  • P Anthony Akkari
  • Ray L Watts
  • Leigh Ragone
  • Mourad Zouari
  • Kelly Lyons
  • Ramu Elango
  • Catherine Wielinski
  • Kevin H Reeves
  • Mounir Kefi
  • Alan Freeman
  • Ghada El Euch-Fayeche
  • David Leppert
  • Samia Ben Yahmed
  • Martha Nance
  • Samia Ben Sassi
  • Rachel A Gibson
  • Christine Hunter
  • Lefkos Middleton
  • Linda Surh
  • Hiroaki Miyajima
  • Tatsuya Hattori
  • Tatsushi Toda
  • Yasuko Hatano
  • Hiroyo Yoshino
  • Eldad Melamed
  • Koichi Mizoguchi
  • Mei Wang
  • Chin Song Lu
  • Kenichi Sato
  • Manabu Funayama
  • Yoko Imamichi
  • Fumiya Obata
  • Kazuko Hasegawa
  • Shin Ichiro Kubo
  • Yuanzhe Li

Detail Information

Publications9

  1. ncbi request reprint Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome
    Neziha Gouider-Khouja
    Service de Neurologie, Institut National de Neurologie, La Rabta, Tunis 1007, Tunisia
    Parkinsonism Relat Disord 8:285-8. 2002
    ..The observation reported in this paper gives evidence that both the disorders are probably two clinical presentations of the same pathogenic process...
  2. ncbi request reprint [Type I glutaric aciduria: an unrecognized cause of progressive dystonia]
    N Gouider-Khouja
    Service de Neurologie Pediatrique, Institut National de Neurologie, Tunis, Tunisie
    Rev Neurol (Paris) 162:858-61. 2006
    ..Cerebral MRI shows large CSF-containing spaces (sylvian fissures and anterior to the temporal lobes) and basal ganglia abnormal signal...
  3. ncbi request reprint Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
    Neziha Gouider-Khouja
    Service de Neurologie, Institut National de Neurologie, La Rabta, Tunis 1007, Tunisia
    Parkinsonism Relat Disord 9:247-51. 2003
    ..To report clinical, pathological and genetic findings in a Tunisian kindred with autosomal recessive juvenile parkinsonism (AR-JP) linked to parkin gene...
  4. doi request reprint Movement disorders in neuro-metabolic diseases
    Neziha Gouider-Khouja
    Department of Child and Adolescent Neurology, Consultation of Movement Disorders and Botulinum Toxin, National Institute of Neurology, Tunis, Tunisia
    Eur J Paediatr Neurol 14:304-7. 2010
    ....
  5. doi request reprint Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child
    Ibtihel Rebai
    Department of Child and Adolescent Neurology, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    Brain Dev 36:921-3. 2014
    ..The disorder severity is due to neurological features and renal complications. Up to now, more than 300 mutations have been reported. We report on a Tunisian child with a severe phenotype due to a novel identified complex mutation. ..
  6. doi request reprint 3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature
    Ichraf Kraoua
    Department of Child and Adolescent Neurology and UR 06 11, National Institute Mongi Ben Hmida of Neurology, Tunis, Tunisia
    Neuropediatrics 44:281-5. 2013
    ..We discuss clinical, biochemical, imaging, electroencephalographic, and therapeutic aspects and review the literature. ..
  7. ncbi request reprint [Neurological complications of acute intermittent porphyria precipitated by porphyrinogenic drugs and efficiency of heme-arginate treatment]
    Rousanna Akopova-Larbi
    Service de Neurologie, Hopital Razi, Manouba, Tunis
    Tunis Med 87:621-6. 2009
    ..Peripheral nervous system manifestations, often precipitated by porphyrinogenic medications are of poor outcome...
  8. ncbi request reprint Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries
    Hiroyuki Tomiyama
    Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan
    Mov Disord 21:1102-8. 2006
    ..Clinical phenotypes including psychosis, dementia, and MIBG ratios are also heterogeneous, similar to neuropathology, in PD associated with LRRK2 mutations...
  9. ncbi request reprint Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families
    Lianna Ishihara
    Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom
    Mov Disord 22:55-61. 2007
    ....