Publications by authors named "Houda Nehdi"

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SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Monia B Hammer, Jinhui Ding, Fanny Mochel, Ghada Eleuch-Fayache, Perrine Charles, Houda Nehdi

Neurodegener Dis· April 2018

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Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia.
Monia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, Moncef Feki, Wieme Maamouri-Hicheri

J Clin Neurosci· February 2014

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Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.
Monia B Hammer, Ghada Eleuch-Fayache, Lucia V Schottlaender, Houda Nehdi, J Raphael Gibbs

Am J Hum Genet· February 2013

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Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families.
Monia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, Dalel Saidi, Amira Nasri

Diagn Mol Pathol· December 2012

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Spinal muscular atrophy due to double gene conversion event.
Wiéme Maamouri, Monia Benhamed Hammer, Yosr Bouhlel, Sihem Souilem, Najla Khmiri, Houda Nehdi

Int J Neurosci· February 2011

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Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis.
Rim Amouri, Houda Nehdi, Yosr Bouhlal, Mounir Kefi, Abdelmajid Larnaout

J Mol Neurosci· November 2009

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