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1

Letters to the editor

Mongi Ben Hamida, Fayçal Hentati, W. Schady, R. J. Meara, John D. England, Austin J. Sumner, William N. Fishbein, S. P. T. Sinkeler, Shin J. Oh, Elliott L. Hurwitz, Kwang W. Lee, Chien W. Chang, Hyo K

Journal:

Year:

1989

Language:

english

File:

PDF, 765 KB

english, 1989

2

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy

Dr. Christiane Ben Hamida, Dr. Nadia Soussi-Yanicostas, Dr. Gillian S. Butler-Browne, Dr. Khemissa Bejaoui, Dr. Fayçal Hentati, Dr. Mongi Ben Hamida

Journal:

Year:

1994

Language:

english

File:

PDF, 1.07 MB

english, 1994

3

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

Baxter, Rachel V., Ben Othmane, Kamel, Rochelle, Julie M., Stajich, Jason E., Hulette, Christine, Dew-Knight, Susan, Hentati, Faycal, Ben Hamida, Mongi, Bel, S., Stenger, Judy E.

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 300 KB

english, 2001

4

Autosomal recessive spastic ataxia of Charlevoix–Saguenay: An overview

Yosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, Fayçal Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2011

Language:

english

File:

PDF, 231 KB

english, 2011

5

Syndrome d’hypertension intracrânienne idiopathique et endocrinopathies : une relation de cause à effet ?

Jeridi, Cyrine, Abdelaziz, Ines Ben, Farhat, Emna, Kharrat, Haifa, Sassi, Samia Ben, Hentati, Fayçal, Zouari, Mourad

Journal:

Revue Neurologique

Year:

2015

Language:

french

File:

PDF, 187 KB

french, 2015

6

Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome

Morgane Stum, Claire-Sophie Davoine, Savine Vicart, Léna Guillot-Noël, Haluk Topaloglu, Francisco Javier Carod-Artal, Hülya Kayserili, Fayçal Hentati, Luciano Merlini, Jon Andoni Urtizberea, EL-Hadi H

Journal:

Year:

2006

Language:

english

File:

PDF, 507 KB

english, 2006

7

Cerebral venous thrombosis in inflammatory bowel disease: a case series

Ben Sassi Samia, Kallel Lamia, Nabli Fatma, Ben Romdhane Sawssen, Ellouze Rim, Zouari Mourad, Ben Romdhane Neila, Filali Azza, Hentati Fayçal

Journal:

International Journal of Colorectal Disease

Year:

2011

Language:

english

File:

PDF, 65 KB

english, 2011

8

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis

Kamel Ben Othmane, Julie M. Rochelle, Mongi Ben Hamida, Brandon Slotterbeck, Nagesh Rao, Faycal Hentati, Margaret A. Pericak-Vance, J. M. Vance

Journal:

Year:

1998

Language:

english

File:

PDF, 243 KB

english, 1998

9

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

Afif Hentati, Karim Ouahchi, Margaret A. Pericak-Vance, Deepak Nijhawan, Arsalan Ahmad, Y. Yang, Jackie Rimmler, W.-Y. Hung, Beate Schlotter, Akhtar Ahmed, Mongi Ben Hamida, Fayçal Hentati, T. Siddiqu

Journal:

Year:

1998

Language:

english

File:

PDF, 90 KB

english, 1998

10

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33

Betsy A. Hosler, Peter C. Sapp, Ralph Berger, Gilmore O'Neill, Khemissa Bejaoui, Mongi Ben Hamida, Faycal Hentati, Wendy Chin, Diane McKenna-Yasek, Jonathan L. Haines, David Patterson, H. Robert Horvi

Journal:

Year:

1998

Language:

english

File:

PDF, 138 KB

english, 1998

11

AllelicROBO3Heterogeneity in Tunisian Patients with Horizontal Gaze Palsy with Progressive Scoliosis

Rim Amouri, Houda Nehdi, Yosr Bouhlal, Mounir Kefi, Abdelmajid Larnaout, Fayçal Hentati

Journal:

Journal of Molecular Neuroscience

Year:

2009

Language:

english

File:

PDF, 352 KB

english, 2009

12

A Novel SACS Gene Mutation in a Tunisian Family

Yosr Bouhlal, Ghada El Euch-Fayeche, Fayçal Hentati, Rim Amouri

Journal:

Journal of Molecular Neuroscience

Year:

2009

Language:

english

File:

PDF, 173 KB

english, 2009

13

Computational Analysis of a Novel SACS Gene Mutation with BioExtract Server

Yosr Bouhlal, Douglas M. Jennewein, Brent Anderson, Joe Reynoldson, Wiem Maamouri, Fayçal Hentati, Rim Amouri, Carol Lushbough

Journal:

Journal of Molecular Neuroscience

Year:

2011

Language:

english

File:

PDF, 395 KB

english, 2011

14

10.1038/1682

Brown, Robert H., Liu, Jing, Aoki, Masashi, Illa, Isabel, Wu, Chenyan, Fardeau, Michel, Angelini, Corrado, Serrano, Carmen, Urtizberea, J. Andoni, Hentati, Faycal, Hamida, Mongi Ben, Bohlega, Saeed, C

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 443 KB

english, 1998

15

Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein

Ouahchi, Karim, Arita, Makoto, Kayden, Herbert, Hentati, Fayçal, Hamida, Mongi Ben, Sokol, Ronald, Arai, Hiroyuki, Inoue, Keizo, Mandel, Jean-Louis, Koenig, Michel

Journal:

Nature Genetics

Year:

1995

File:

PDF, 601 KB

1995

16

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35

Hentati, Afif, Bejaoui, Khemissa, Pericak-Vance, Margaret A., Hentati, Faycal, Speer, Marcy C., Hung, Wu-Yen, Figlewicz, Denise A., Haines, Jonathan, Rimmler, Jackie, Ben Hamida, Christiane

Journal:

Nature Genetics

Year:

1994

File:

PDF, 485 KB

1994

17

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration

Maria K. Tsaousidou, Karim Ouahchi, Tom T. Warner, Yi Yang, Michael A. Simpson, Nigel G. Laing, Philip A. Wilkinson, Ricardo E. Madrid, Heema Patel, Faycal Hentati, Michael A. Patton, Afif Hentati, Ph

Journal:

The American Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 488 KB

english, 2008

18

Discrepancies of NKT cells expression in peripheral blood and in cerebrospinal fluid from Behçet's disease

Kamel Hamzaoui, Mariam Kamoun, Habib Houman, Fayçal Hentati, M'Hamed Hamza, Khaled Ayed, Agnes Hamzaoui

Journal:

Journal of Neuroimmunology

Year:

2006

Language:

english

File:

PDF, 239 KB

english, 2006

19

BAFF is up-regulated in central nervous system of neuro-Behçet's disease

Kamel Hamzaoui, Habib Houman, Faycal Hentati, Agnes Hamzaoui

Journal:

Journal of Neuroimmunology

Year:

2008

Language:

english

File:

PDF, 166 KB

english, 2008

20

Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders

Richard P. Copp, Thomas Wisniewski, Fayçal Hentati, Abdelmajid Larnaout, Mongi Ben Hamida, Herbert J. Kayden

Journal:

Year:

1999

Language:

english

File:

PDF, 1.04 MB

english, 1999

21

The ancestry of LRRK2 Gly2019Ser parkinsonism – Authors' reply

Matthew J Farrer, Rachel Gibson, Fayçal Hentati

Journal:

The Lancet Neurology

Year:

2008

Language:

english

File:

PDF, 49 KB

english, 2008

22

Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13

Jing Liu, Chenyan Wu, Karen Bossie, Khemissa Bejaoui, Betsy A. Hosler, Jeffrey C. Gingrich, Mongi Ben Hamida, Faycal Hentati, Erwin Schurr, Pieter J. de Jong, Robert H. Brown Jr.

Journal:

Year:

1998

Language:

english

File:

PDF, 152 KB

english, 1998

23

Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15

Kamel Ben Othmane, Ellen Johnson, Marisa Menold, Felicia L. Graham, Mongi Ben Hamida, Osamu Hasegawa, Allison D. Rogala, Akio Ohnishi, Margaret Pericak-Vance, Faycal Hentati, Jeffery M. Vance

Journal:

Year:

1999

Language:

english

File:

PDF, 199 KB

english, 1999

24

Progress in Neuropathology of the Neuronal Ceroid Lipofuscinoses

Hans H. Goebel, Sydney S. Schochet, Margaret Jaynes, Wolfgang Brück, Alfried Kohlschütter, Faycal Hentati

Journal:

Molecular Genetics and Metabolism

Year:

1999

Language:

english

File:

PDF, 521 KB

english, 1999

25

Cerebral Venous Thrombosis Presenting With Cerebellar Ataxia and Cortical Blindness

Samia Ben Sassi, Habiba Mizouni, Fatma Nabli, Lamia Kallel, Mounir Kefi, Fayçal Hentati

Journal:

Journal of Stroke and Cerebrovascular Diseases

Year:

2010

Language:

english

File:

PDF, 317 KB

english, 2010

26

Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa

Kenya Nishioka, Carles Vilariño-Güell, Stephanie A. Cobb, Jennifer M. Kachergus, Owen A. Ross, Christian Wider, Rachel A. Gibson, Faycal Hentati, Matthew J. Farrer

Journal:

Neuroscience Letters

Year:

2010

Language:

english

File:

PDF, 335 KB

english, 2010

27

Professor Mongi Ben Hamida (1928–2003)

Fayçal Hentati

Journal:

Neuromuscular Disorders

Year:

2003

Language:

english

File:

PDF, 94 KB

english, 2003

28

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson’s disease

Kenya Nishioka, Carles Vilariño-Güell, Stephanie A. Cobb, Jennifer M. Kachergus, Owen A. Ross, Emna Hentati, Faycal Hentati, Matthew J. Farrer

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 146 KB

english, 2010

29

Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease

Samia Ben Sassi, Fatma Nabli, Emna Hentati, Houda Nahdi, Meriam Trabelsi, Hela Ben Ayed, Rim Amouri, John Eric Duda, Matthew John Farrer, Fayçal Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2012

Language:

english

File:

PDF, 123 KB

english, 2012

30

Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease

Nadia Ammar, Eva Nelis, Luciano Merlini, Nina Barišić, Rim Amouri, Chantal Ceuterick, Jean-Jacques Martin, Vincent Timmerman, Fayçal Hentati, Peter De Jonghe

Journal:

Neuromuscular Disorders

Year:

2003

Language:

english

File:

PDF, 542 KB

english, 2003

31

Clinical and genetic aspects of autosomal recessive CMT

Kamel Ben Othmane, Julie M. Rochelle, Ellen Johnson, Mongi Ben Hamida, Margaret A. Pericak-Vance, Faycal Hentati, Jeffery M. Vance

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 263 KB

english, 1997

32

Friedreich's ataxia phenotype with vitamin E deficiency (FAVED): an overview

Fayçal Hentati

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 133 KB

english, 1997

33

Cognitive and psychological profile of a Tunisian population of limb girdle muscular dystrophy

Najoua Miladi, Jean-Pierre Bourguignon, Fayçal Hentati

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 31 KB

english, 1999

34

Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome

Neziha Gouider-Khouja, Aouatef Mekaouar, Abdelmajid Larnaout, Najoua Miladi, Fethi Ben Khelifa, Fayçal Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2002

Language:

english

File:

PDF, 193 KB

english, 2002

35

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study

Neziha Gouider-Khouja, Abdelmajid Larnaout, Rim Amouri, Sana Sfar, Samir Belal, Christiane Ben Hamida, Mongi Ben Hamida, Nobutaka Hattori, Yoshikuni Mizuno, Fayçal Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2003

Language:

english

File:

PDF, 99 KB

english, 2003

36

Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis

Mongi Ben Hamida, Fethi Letaief, Fayçal Hentati, Christiane Ben Hamida

Journal:

Journal of the Neurological Sciences

Year:

1987

Language:

english

File:

PDF, 1.37 MB

english, 1987

37

A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia

Sihem Souilem, Saber Chebel, Michelangelo Mancuso, Lucia Petrozzi, Gabriele Siciliano, Mahbouba FrihAyed, Faycal Hentati, Rim Amouri

Journal:

Journal of the Neurological Sciences

Year:

2011

Language:

english

File:

PDF, 596 KB

english, 2011

38

A gliotoxic factor and multiple sclerosis

Armelle Ménard, Rim Amouri, Tomáš Dobránsky, Christiane Charriaut-Marlangue, Régine Pierig, Carmen Cifuentes-Diaz, Said Ghandour, James Belliveau, Hughes Gascan, Fayçal Hentati, Olivier Lyon-Caen, Her

Journal:

Journal of the Neurological Sciences

Year:

1998

Language:

english

File:

PDF, 1.42 MB

english, 1998

39

[Handbook of Clinical Neurology] Peripheral Nerve Disorders Volume 115 || Giant axonal neuropathy

Hentati, Fayçal

Year:

2013

Language:

english

File:

PDF, 1.76 MB

english, 2013

40

Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia

Hammer, Monia Benhamed, El Euch-Fayache, Ghada, Nehdi, Houda, Feki, Moncef, Maamouri-Hicheri, Wieme, Hentati, Fayçal, Amouri, Rim

Journal:

Journal of Clinical Neuroscience

Year:

2014

Language:

english

File:

PDF, 1.28 MB

english, 2014

41

[Handbook of Clinical Neurology] Ataxic Disorders Volume 103 || Ataxia with vitamin E deficiency and abetalipoproteinemia

Hentati, Fayçal

Year:

2012

Language:

english

File:

PDF, 180 KB

english, 2012

42

Atrophie cérébelleuse révélant un lupus érythémateux systémique : à propos d’une observation

Zouari, Mourad, Zangar, Emna, H’mida, Intissar, Hentati, Faycal

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 58 KB

french, 2012

43

Abstracts of Current Literature

Zouari, Mourad, Zangar, Emna, H’mida, Intissar, Hentati, Faycal

Journal:

Journal of Vascular and Interventional Radiology

Year:

1998

Language:

english

File:

PDF, 1.95 MB

english, 1998

44

Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome

Sassi, Samia Ben, Nabli, Fatma, Boubaker, Adnene, Ghorbel, Imed Ben, Neji, Sonia, Hentati, Fayçal

Journal:

Journal of the Neurological Sciences

Year:

2014

Language:

english

File:

PDF, 403 KB

english, 2014

45

Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum

Hentati, Fayçal, Hamida, Christiane Ben, Zeghal, Mohamed, Kamoun, Mohamed, Fezaa, Bassima, Hamida, Mongi Ben

Journal:

Neuromuscular Disorders

Year:

1992

Language:

english

File:

PDF, 898 KB

english, 1992

46

STX6 rs1411478 is not associated with increased risk of Parkinson's disease

Trinh, Joanne, Vilariño-Güell, Carles, Donald, Alan, Shah, Brinda, Yu, Irene, Szu-Tu, Chelsea, Aasly, Jan O., Wu, Ruey-Meei, Hentati, Faycal, Rajput, Ali H., Rajput, Alex, Farrer, Matthew J.

Journal:

Parkinsonism & Related Disorders

Year:

2013

Language:

english

File:

PDF, 115 KB

english, 2013

47

Lymphome primitif suprasellaire : à propos d’un cas

Lakhdar, Iness, Ben Sassi, Samia, Bekri, Iméne, Walha, Kamel, Néji, Sonia, Boubaker, Adnéne, Hentati, Fayçal

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 73 KB

french, 2012

48

HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)

HAMIDA, MONGI BEN, HENTATI, FAYÇAL, HAMIDA, CHRISTIANE BEN

Journal:

Year:

1990

Language:

english

File:

PDF, 2.98 MB

english, 1990

49

Autosomal Recessive Ataxia Caused by Three Distinct Gene Defects in a Single Consanguineous Family

Bouhlal, Yosr, Zouari, Mourad, Kefi, Mounir, Hamida, Christiane Ben, Hentati, Fayçal, Amouri, Rim

Journal:

Journal of Neurogenetics

Year:

2008

Language:

english

File:

PDF, 308 KB

english, 2008

50

Peripheral neuropathy in inflammatory bowel disease patients: A prospective cohort study

Sassi, Samia Ben, Kallel, Lamia, Ben Romdhane, Sawssen, Boubaker, Jalel, Filali, Azza, Hentati, Fayçal

Journal:

Scandinavian Journal of Gastroenterology

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

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