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Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982.
Arch Neurol. 2003.
PMID: 12873855
Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency.
El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F.
El Euch-Fayache G, et al.
Brain. 2014 Feb;137(Pt 2):402-10. doi: 10.1093/brain/awt339. Epub 2013 Dec 25.
Brain. 2014.
PMID: 24369383
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Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.
Hammer MB, Eleuch-Fayache G, Gibbs JR, Arepalli SK, Chong SB, Sassi C, Bouhlal Y, Hentati F, Amouri R, Singleton AB.
Hammer MB, et al.
Eur J Neurol. 2013 Mar;20(3):486-492. doi: 10.1111/j.1468-1331.2012.03883.x. Epub 2012 Oct 9.
Eur J Neurol. 2013.
PMID: 23043354
Free PMC article.
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Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia.
Hammer MB, El Euch-Fayache G, Nehdi H, Feki M, Maamouri-Hicheri W, Hentati F, Amouri R.
Hammer MB, et al. Among authors: el euch fayache g.
J Clin Neurosci. 2014 Feb;21(2):311-5. doi: 10.1016/j.jocn.2013.04.016. Epub 2013 Oct 16.
J Clin Neurosci. 2014.
PMID: 24139731
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Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.
Hammer MB, Eleuch-Fayache G, Schottlaender LV, Nehdi H, Gibbs JR, Arepalli SK, Chong SB, Hernandez DG, Sailer A, Liu G, Mistry PK, Cai H, Shrader G, Sassi C, Bouhlal Y, Houlden H, Hentati F, Amouri R, Singleton AB.
Hammer MB, et al.
Am J Hum Genet. 2013 Feb 7;92(2):245-51. doi: 10.1016/j.ajhg.2012.12.012. Epub 2013 Jan 17.
Am J Hum Genet. 2013.
PMID: 23332917
Free PMC article.
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Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families.
Hammer MB, El Euch-Fayache G, Nehdi H, Saidi D, Nasri A, Nabli F, Bouhlal Y, Maamouri-Hicheri W, Hentati F, Amouri R.
Hammer MB, et al. Among authors: el euch fayache g.
Diagn Mol Pathol. 2012 Dec;21(4):241-5. doi: 10.1097/PDM.0b013e318257ad9a.
Diagn Mol Pathol. 2012.
PMID: 23111195
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SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Hammer MB, Ding J, Mochel F, Eleuch-Fayache G, Charles P, Coutelier M, Gibbs JR, Arepalli SK, Chong SB, Hernandez DG, Majounie E, Clipman S, Bouhlal Y, Nehdi H, Brice A, Hentati F, Stevanin G, Amouri R, Durr A, Singleton AB.
Hammer MB, et al.
Neurodegener Dis. 2017;17(4-5):208-212. doi: 10.1159/000464445. Epub 2017 May 31.
Neurodegener Dis. 2017.
PMID: 28558379
Free PMC article.
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