Letter to the editor: “A case of Guillain-Barré syndrome with meningeal irritation” von Rebai, Ibtihel, Ben Achour, Nedia, El Mabrouk, Emna, Kraoua, Ichraf, Ben Youssef-Turki, Ilhem

Volltext

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood von Rebai, Ibtihel, Ben Rhouma, Hanene, Kraoua, Ichraf, Klaa, Hedia, Rouissi, Aida, Ben Youssef-Turki, Ilhem, Gouider-Khouja, Neziha

Volltext

Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia von Ben Achour, Nedia, Mrabet, Saloua, Rebai, Ibtihel, Abid, Ines, Benrhouma, Hanene, Klaa, Hedia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef Turki, Ilhem

Volltext

Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child von Rebai, Ibtihel, Kraoua, Ichraf, Benrhouma, Hanene, Rouissi, Aida, Turki, Ilhem, Ceballos-Picot, Irène, Gouider-Khouja, Neziha

Volltext

Mirror movements and myelomeningocele: report of a single case and review of literature von Rébai, Ibtihel, Benrhouma, Hanene, Kraoua, Ichraf, Drissi, Cyrine, Ben Hammouda, Mohammed, Gouider-Khouja, Neziha

Volltext

Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review von Ben Achour, Nedia, Ben Younes, Thouraya, Rebai, Ibtihel, Ben Ahmed, Melika, Kraoua, Ichraf, Ben Youssef–Turki, Ilhem

Volltext

Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years von Ben Youssef Turki, Ilhem, Rouissi, Aida, Klaa, Hedia, Benrhouma, Hanene, Raddadi, Sarra, Rebai, Ibtihel, Ben Achour, Nedia, Kraoua, Ichraf

Volltext

Aspects radiologiques des encéphalites limbiques autoimmunes chez l’enfant von Rebai, Ibtihel, Ben, Achour Nadia, Benrhouma, Hanene, Drissi, Cyrine, Hamouda, Mohamed Ben, Kraoua, Ichraf, Turki, Ilhem

Volltext

Particularités du traitement des dystonies focales par la Toxine Botulique : étude descriptive sur 8 ans von Benrhouma, Hanene, Salma, Askri, Klaa, Hedia, Ibtihel, Rebai, Neziha, Gouider Khouja, Kraoua, Ichraf, Turki, Ilhem

Volltext

Accidents vasculaires cérébraux secondaires aux vascularités du système nerveux central chez l’enfant von Yengui, Nahla, Rebai, Ibtihel, Hammami, Nadia, Benrhouma, Hanene, Hamouda, Mohamed Ben, Kraoua, Ichraf, Turki, Ilhem

Volltext

Encéphalites limbiques auto-immunes post-herpétiques : un véritable challenge diagnostique von Makhlouf, Sinda, Achour, Nedia Ben, Benrhouma, Hanene, Rebai, Ibtihel, Klaa, Hedia, Kraoua, Ichraf, Turki, Ilhem

Volltext

Profils neurocognitifs précoces au cours de la sclérose en plaques à début pédiatrique von Rebai, Ibtihel, Achour, Nedia Ben, Benrhouma, Hanene, Imene, Mejri, Klaa, Hedia, Kraoua, Ichraf, Turki, Ilhem

Volltext

Syndrome d’Allgrove: à propos de 2 cas pédiatriques von Elmabrouk, Emna, Rouissi, Aida, Benrhouma, Hanene, Achour, Nedia Ben, Ibtihel, Rebai, Kraoua, Ichraf, Turki, Ilhem

Volltext

Cérébellite aiguë chez l’enfant von Younes, Thouraya Ben, Klaa, Hedia, Benrhouma, Hanene, Ibtihel, Rebai, Achour, Nedia Ben, Kraoua, Ichraf, Turki, Ilhem

Volltext

Accidents vasculaires cérébraux secondaires aux hémopathies chez l’enfant von Yengui, Nahla, Rebai, Ibtihel, Benrhouma, Hanene, Ben, Achour Nadia, Rouissi, Aida, Kraoua, Ichraf, Turki, Ilhem

Volltext

Spectre des neuronopathies motrices chez l’enfant: étude monocentrique de 46 cas von Achour, Nedia Ben, Brahem, Zeineb, Benrhouma, Hanene, Rebai, Ibtihel, Klaa, Hedia, Kraoua, Ichraf, Turki, Ilhem

Volltext

Neuro-imagerie des maladies lysosomales von Rebai, Ibtihel, Kraoua, Ichraf, Drissi, Cyrine, Benrhouma, Hanene, Turki, Ilhem, Ben Hamouda, Mohamed, Gouider-Khouja, Neziha

Volltext

Mirror movements and myelomeningocele: report of a single case and review of literature von Rébai, Ibtihel, Benrhouma, Hanene, Kraoua, Ichraf, Drissi, Cyrine, Ben Hammouda, Mohammed, Gouider-Khouja, Neziha

Volltext

Polymorphisms in XRCC1, ERCC2, and ERCC3 DNA repair genes, CYP1A1 xenobiotic metabolism gene, and tobacco are associated with bladder cancer susceptibility in Tunisian population von Feki-Tounsi, Molka, Khlifi, Rim, Louati, Ibtihel, Fourati, Mohamed, Mhiri, Mohamed-Nabil, Hamza-Chaffai, Amel, Rebai, Ahmed

Volltext

Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure von M'dimegh, Saoussen, PhD, Omezzine, Asma, PhD, Hamida-Rebai, Mériam Ben, Aquaviva-bourdain, Cécile, PharmD, PhD, M'barek, Ibtihel, PhD, Sahtout, Wissal, Zellama, Dorsaf, Souche, Geneviéve, Achour, Abdellatif, Abroug, Saoussen, MD, Bouslama, Ali

Volltext