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. ncbi 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. ncbi 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
  6. 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
  7. 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
  8. 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
  • Rousanna Akopova-Larbi
  • Lianna Ishihara
  • Faycal Hentati
  • Hiroyuki Tomiyama
  • Lilia Kraoua
  • Ilhem Turki
  • Gilbert Briand
  • Fehmi Nasrallah
  • Habiba Chaabouni
  • Elsa Wiame
  • Hanen Benrhouma
  • Naziha Kaabachi
  • Aida Rouissi
  • Riadh Gouider
  • Turki Ilhem Ben Youssef
  • Amina Gargouri
  • Siwan Thomas
  • Jina E Swartz
  • Kevin H Reeves
  • Alan Freeman
  • Kelly Lyons
  • Leigh Ragone
  • David Leppert
  • Samia Ben Yahmed
  • Rachel A Gibson
  • Mounir Kefi
  • Linda Surh
  • Ghada El Euch-Fayeche
  • P Anthony Akkari
  • Samia Ben Sassi
  • Martha Nance
  • Lefkos Middleton
  • Christine Hunter
  • Ray L Watts
  • Mourad Zouari
  • Liling Warren
  • Catherine Wielinski
  • Ramu Elango
  • Tatsushi Toda
  • Fumiya Obata
  • Yasuko Hatano
  • Kazuko Hasegawa
  • Koichi Mizoguchi
  • Shin Ichiro Kubo
  • Manabu Funayama
  • Hiroaki Miyajima
  • Mei Wang
  • Tatsuya Hattori
  • Kenichi Sato
  • Chin Song Lu
  • Hiroyo Yoshino
  • Yuanzhe Li
  • Yoko Imamichi
  • Eldad Melamed

Detail Information

Publications8

  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. ncbi 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. ncbi 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. ..
  6. 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...
  7. 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...
  8. 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
    ....