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51

Optical and scanning electron microscopies cross-fertilization : Application to worn carbon/carbon composite surface studies

B. Rousseau, H. Estrade-Szwarckopf, S. Bonnamy, M. Gouider, Y. Berthier, P. Jacquemard

Journal:

Year:

2005

Language:

english

File:

PDF, 306 KB

english, 2005

52

Impact of orthophosphate addition on biofilm development in drinking water distribution systems

Mbarka Gouider, Jalel Bouzid, Sami Sayadi, Antoine Montiel

Journal:

Journal of Hazardous Materials

Year:

2009

Language:

english

File:

PDF, 352 KB

english, 2009

53

Separative recovery with lime of phosphate and fluoride from an acidic effluent containing H3PO4, HF and/or H2SiF6

Mbarka Gouider, Mongi Feki, Sami Sayadi

Journal:

Journal of Hazardous Materials

Year:

2009

Language:

english

File:

PDF, 663 KB

english, 2009

54

High body mass index is an independent predictor of differentiation syndrome in patients with acute promyelocytic leukemia

Ramzi Jeddi, Hèla Ghédira, Samia Mnif, Emna Gouider, Pierre Fenaux, Balkis Meddeb

Journal:

Leukemia Research

Year:

2010

Language:

english

File:

PDF, 109 KB

english, 2010

55

Coexistence d’un rhumatisme psoriasique et d’une colite collagène avec une maladie inflammatoire du système nerveux

Dhouha Azzouz, Amina Gargouri, Wafa Hamdi, Hela Kchir, Yosr Hizem, Raoudha Tekaya, Mouna Ben Djebara, Riadh Gouider, Mohamed Montacer Kchir

Journal:

Revue du Rhumatisme

Year:

2008

Language:

french

File:

PDF, 68 KB

french, 2008

56

P113 Chronic myelomonocytic leukemia with monosomy 7 after successful treatment of acute promyelocytic leukemia

R. Jeddi, E. Gouider, H. Ben Neji, S. Mnif, L. Aissaoui, K. Kacem, R. Ben Amor, R. Ben Lakhal, H. Ben Abid, Z. Belhadjali, B. Meddeb

Journal:

Leukemia Research

Year:

2007

Language:

english

File:

PDF, 55 KB

english, 2007

57

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency

S. Gabsi, N. Gouider-Khouja, S. Belal, M. Fki, M. Kefi, I. Turki, M. Ben Hamida, H. Kayden, R. Mebazaa, F. Hentati

Journal:

European Journal of Neurology

Year:

2001

Language:

english

File:

PDF, 86 KB

english, 2001

58

Terahertz photoconductivity of a two-dimensional electron gas in HgCdTe/HgTe quantum wells

Yu. B. Vasilyev, F. Gouider, M. Bugár, G. Nachtwei, J. Könemann, C. Brüne, H. Buhmann

Journal:

physica status solidi (b)

Year:

2010

Language:

english

File:

PDF, 115 KB

english, 2010

59

Terahertz photoresponse dependence on magnetic and electric fields in graphene-based devices

M. Salman, F. Gouider, H. Schmidt, Yu. B. Vasilyev, R. J. Haug, G. Nachtwei

Journal:

physica status solidi (c)

Year:

2011

Language:

english

File:

PDF, 187 KB

english, 2011

60

A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13

Sara C. Meyer, Ramzi Jeddi, Balkis Meddeb, Emna Gouider, Bernhard Lämmle, Johanna A. Kremer Hovinga

Journal:

Annals of Hematology

Year:

2008

Language:

english

File:

PDF, 90 KB

english, 2008

61

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity

O. Messaoud, M. Ben Rekaya, H. Ouragini, S. Benfadhel, H. Azaiez, R. Kefi, N. Gouider-Khouja, I. Mokhtar, A. Amouri, M. S. Boubaker, M. Zghal, S. Abdelhak

Journal:

Archives of Dermatological Research

Year:

2012

Language:

english

File:

PDF, 380 KB

english, 2012

62

Magnetotransport and THz-Optical Investigations at

F. Gouider, Y. B. Vasilyev, M. Bugár, J. Könemann, C. Brüne, H. Buhmann, G. Nachtwei

Journal:

Journal of Low Temperature Physics

Year:

2010

Language:

english

File:

PDF, 388 KB

english, 2010

63

The Transesophageal Echocardiographic Diagnosis of Left Atrial Myxoma Simulating a Left Atrial Thrombus in the Setting of Mitral Stenosis

Abdallah Mahdhaoui, Hatem Bouraoui, Majdoub Mohamed Amine, Moncef Mokni M., Trimeche Besma, Samia Ernez Hajri, Gouider Jeridi, Mabrouk Khelfa, Fathi Bahri, Tahar Yacoubi, Badreddine Sriha B., Habib Am

Journal:

Echocardiography

Year:

2004

Language:

english

File:

PDF, 129 KB

english, 2004

64

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family

O. Messaoud, M. Ben Rekaya, R. Kefi, S. Chebel, A. Boughammoura-Bouatay, H. Bel Hadj Ali, N. Gouider-Khouja, J. Zili, M. Frih-Ayed, I. Mokhtar, S. Abdelhak, M. Zghal

Journal:

British Journal of Dermatology

Year:

2010

Language:

english

File:

PDF, 173 KB

english, 2010

65

Small insertion (c.869insC) within F13A gene is dominant in Tunisian patients with inherited FXIII deficiency due to ancient founder effect

H. EL MAHMOUDI, M. B. AMOR, E. GOUIDER, R. HORCHANI, R. HAFSIA, K. FADHLAOUI, B. MEDDEB, A. HAFSIA, A. B. AMMAR EL GAAIED

Journal:

Year:

2009

Language:

english

File:

PDF, 94 KB

english, 2009

66

Molecular analysis in two Tunisian families with combined factor V and factor VIII deficiency

H. E. ABDALLAH, E. GOUIDER, M. B. AMOR, A. JLIZI, B. MEDDEB, A. ELGAAIED

Journal:

Year:

2010

Language:

english

File:

PDF, 564 KB

english, 2010

67

Identification of novel and recurrent mutations in Tunisian haemophilia B patients

H. ELMAHMOUDI, H. KHODJET-EL-KHIL, M. BEN-AMOR, A. JLIZI, K. ZAHRA, B. MEDDEB, A. BEN-AMMAR- EL-GAAIED, E. GOUIDER

Journal:

Year:

2011

Language:

english

File:

PDF, 52 KB

english, 2011

68

Analysis of newly detected mutations in the MCFD2 gene giving rise to combined deficiency of coagulation factors V and VIII

H. ELMAHMOUDI, E. WIGREN, A. LAATIRI, A. JLIZI, A. ELGAAIED, E. GOUIDER, Y. LINDQVIST

Journal:

Year:

2011

Language:

english

File:

PDF, 205 KB

english, 2011

69

A recommended treatment algorithm in relapsing multiple sclerosis: report of an international consensus meeting

D. Karussis, L. D. Biermann, S. Bohlega, A. Boiko, M. Chofflon, F. Fazekas, M. Freedman, S. Gebeily, R. Gouider, E. Havrdova, G. Jakab, R. Karabudak, A. Miller, the International Working Group for Tre

Journal:

European Journal of Neurology

Year:

2006

Language:

english

File:

PDF, 165 KB

english, 2006

70

Familial form of typical childhood absence epilepsy in a consanguineous context

Hanen Abouda, Yosr Hizem, Amina Gargouri, Christel Depienne, Delphine Bouteiller, Florence Riant, Elisabeth Tournier-Lasserve, Isabelle Gourfinkel-An, Eric LeGuern, Riadh Gouider

Journal:

Year:

2010

Language:

english

File:

PDF, 207 KB

english, 2010

71

The cyclotron resonance in Heterostructures with the InSb/AlInSb quantum wells

Yu. B. Vasilyev, F. Gouider, G. Nachtwei, P. D. Buckle

Journal:

Year:

2010

Language:

english

File:

PDF, 217 KB

english, 2010

72

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

O. Dubourg, H. Azzedine, C. Verny, G. Durosier, N. Birouk, R. Gouider, M. Salih, A. Bouhouche, A. Thiam, D. Grid, M. Mayer, M. Ruberg, M. Tazir, A. Brice, E. LeGuern

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 166 KB

english, 2006

73

Novel Mutations in the C-Terminal Region of the MECP2 Gene in Tunisian Rett Syndrome Patients

Fendri-Kriaa, N., Rouissi, A., Ghorbel, R., Mkaouar-Rebai, E., Belguith, N., Gouider-Khouja, N., Fakhfakh, F.

Journal:

Journal of Child Neurology

Year:

2012

Language:

english

File:

PDF, 316 KB

english, 2012

74

Retention of copper and nickel from aqueous solutions using manganese oxide-coated burned brick

N. Boujelben, M. Gouider, Z. Elouear, J. Bouzid, M. Feki, A. Montiel

Journal:

Environmental Progress & Sustainable Energy

Year:

2012

Language:

english

File:

PDF, 199 KB

english, 2012

75

Hot water epilepsy with pachygyria

Yosr Hizem, Amina Gargouri, Mouna Ben Djebara, Imen Kacem, Istabrak Abdelkefi, Fethi Jemli, Riadh Gouider

Journal:

Neurological Sciences

Year:

2012

Language:

english

File:

PDF, 197 KB

english, 2012

76

Methylmalonic acidemia and hyperglycemia: An unusual association

Marouani Imen, Benrhouma Hanene, Kraoua Ichraf, Rouissi Aida, Turki Ilhem, Kaabachi Naziha, Gouider-Khouja Neziha

Journal:

Brain and Development

Year:

2012

Language:

english

File:

PDF, 81 KB

english, 2012

77

Movement disorders in neuro-metabolic diseases

Neziha Gouider-Khouja, Ichraf Kraoua, Hanene Benrhouma, Narjes Fraj, Aida Rouissi

Journal:

European Journal of Paediatric Neurology

Year:

2010

Language:

english

File:

PDF, 178 KB

english, 2010

78

179 Results of a trial of prednisone treatment in limb girdle muscular dystrophy 2

F. Belhassen, N. Gouider-Khouja, M. Kefi, R. Amouri, S. Kobbi, N. Miladi, M. Ben Hamida, F. Hentati

Journal:

European Journal of Paediatric Neurology

Year:

1999

Language:

english

File:

PDF, 130 KB

english, 1999

79

Mechanism of terahertz photoconductivity in semimetallic HgTe/CdHgTe quantum wells

Vasilyev, Yu. B., Mikhailov, N. N., Gouider, F., Vasilyeva, G. Yu., Nachtwei, G.

Journal:

Year:

2012

Language:

english

File:

PDF, 173 KB

english, 2012

80

Factor VIII haplotypes frequencies in Tunisian hemophiliacs A

Hejer Elmahmoudi, Nejla Belhedi, Asma Jlizi, Kaouther Zahra, Balkis Meddeb, Amel Ben Ammar Elgaaied, Emna Gouider

Journal:

Diagnostic Pathology

Year:

2011

Language:

english

File:

PDF, 212 KB

english, 2011

81

Neurophysiologic investigations in symptomatic and asymptomatic neurofibromatosis type I (NF1) patients

R. Gouider, A. Mrabet, M. Kchouk, L. Lasram, A.Ben Osman, M. Azaiz

Journal:

Electroencephalography and Clinical Neurophysiology

Year:

1993

Language:

english

File:

PDF, 193 KB

english, 1993

82

M25 Intrafamilial variations of motor nerve conduction in CMT1A patients

N. Birouk, R. Gouider, M. Gugenheim, E. Le Guern, A. Brice, P. Bouche

Journal:

Electroencephalography and Clinical Neurophysiology

Year:

1996

Language:

english

File:

PDF, 138 KB

english, 1996

83

SS-3-5 SR-57746A, a growth factor like compound. Dose ranging study of the efficacy using muscle testing and repeated measures of EMG variables in amyotrophic lateral sclerosis (ALS)

Lucette Lacomblez, Thierry Maisonnobe, Riadh Gouider, Valérie Doppler, François Salachas, Nasa Birouk, Patrice Douillet, Gilbert Bensimon, Pierre Bouche, Vincent Meininger

Journal:

Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control

Year:

1995

Language:

english

File:

PDF, 128 KB

english, 1995

84

Structural analysis of two novel mutations in MCFD2 gene causing combined coagulation factors V and VIII deficiency

Hejer Elmahmoudi Abdallah, Emna Gouider, Nejla Stambouli, Mohamed Ben Amor, Asma Jlizi, Nejla Belhedi, Rim Sassi, Houssein Khodjetelkhil, Balkis Meddeb, Raouf Hafsia, Adel Hamza, Amel Benammar Elgaaie

Journal:

Blood Cells, Molecules, and Diseases

Year:

2010

Language:

english

File:

PDF, 1.96 MB

english, 2010

85

Bioassay and use in irrigation of untreated and treated wastewaters from phosphate fertilizer industry

Mbarka Gouider, Mongi Feki, Sami Sayadi

Journal:

Ecotoxicology and Environmental Safety

Year:

2010

Language:

english

File:

PDF, 477 KB

english, 2010

86

A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia

Ines Ouertani, Myriam Chaabouni, Ilhem Turki, Marc Lelorc'h, Tania Attié-Bitach, Lamia Ben Jemaa, Neziha Khouja-Gouider, Habiba Chaabouni

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 199 KB

english, 2009

87

Novel double deletions in the MECP2 gene in Tunisian Rett patient

Nourhene Fendri-Kriaa, Aida Rouissi, Rania Ghorbel, Emna Mkaouar-Rebai, Neila Belguith, Naziha Gouider-Khouja, Faiza Fakhfakh

Journal:

Year:

2012

Language:

english

File:

PDF, 887 KB

english, 2012

88

Peripheral myoclonus and muscle hypertrophy of quadriceps revealing a spinal dysraphism

N. Gouider-Khouja, S. Gabsi-Gherairi

Journal:

Parkinsonism & Related Disorders

Year:

2009

Language:

english

File:

PDF, 287 KB

english, 2009

89

Secondary chronic myelomonocytic leukemia with monosomy 7 after successful treatment of acute promyelocytic leukemia

R. Jeddi, E. Gouider, H. Benneji, S. Mnif, H. Ben Abid, Z. Belhadjali, B. Meddeb

Journal:

Pathologie Biologie

Year:

2008

Language:

english

File:

PDF, 89 KB

english, 2008

90

Transfusion-related acute lung injury (TRALI) during remission induction course of acute myeloid leukemia: A possible role for all-transretinoic-acid (ATRA)?

R. Jeddi, R. Mansouri, K. Kacem, E. Gouider, H.B. Abid, Z. Belhadjali, B. Meddeb

Journal:

Pathologie Biologie

Year:

2009

File:

PDF, 137 KB

2009

91

Neuroancanthocytose : un diagnostic à ne pas méconnaître

T. Larbi, M. Abdallah, E. Gouider, L. Ben Farhat, S. Hamzaoui, A. Harmel, M. Ennafaa, K. Bouslama, N. Gouider, S. M'Rad, M. Ben Dridi

Journal:

La Revue de Médecine Interne

Year:

2007

Language:

french

File:

PDF, 54 KB

french, 2007

92

Infections par des virus transmissibles par le sang chez des hémophiles en Tunisie

H. Langar, H. Triki, E. Gouider, O. Bahri, A. Djebbi, A. Sadraoui, A. Hafsia, R. Hafsia

Journal:

Transfusion Clinique et Biologique

Year:

2005

Language:

french

File:

PDF, 102 KB

french, 2005

93

Polyradiculonévrite et sarcoïdose

M Fredj, I Ben Ghorbel, M Jebloun, R Gouider, A Mrabet

Journal:

La Revue de Médecine Interne

Year:

1998

File:

PDF, 223 KB

1998

94

Syndromes de défibrination atypiques et leucémies aiguës à translocation t(9,22) ; à propos de deux observations

B Meddeb, S Guermazi, R Hafsia, H Ben Abid, E Gouider, R Ben Lakhal, Z Bel Haj Ali, T Ben Othman, R Jeddi, K Dellagi, A Hafsia

Journal:

Pathologie Biologie

Year:

2001

Language:

french

File:

PDF, 61 KB

french, 2001

95

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3

A. Driss, R. Amouri, C. Ben Hamida, S. Souilem, N. Gouider-Khouja, M. Ben Hamida, F. Hentati

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 348 KB

english, 2000

96

The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity

O Dubourg, S Tardieu, N Birouk, R Gouider, J.M Léger, T Maisonobe, A Brice, P Bouche, E LeGuern

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 110 KB

english, 2001

97

Polyneuropathy in 8 glue-sniffers

I. Turki, O. Ben Nefissa, F. Kechrid, N. Gouider-Khouja, S. Belal, F. Hentati, M. Ben Hamida

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 134 KB

english, 1997

98

Congenital myasthenic syndromes

N. Gouider-Khouja, I. Turki, S. Oueslati, N. Miladi, M. Ben Hamida, F. Hentati

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 136 KB

english, 1997

99

Mitochondrial myopathy with demyelination polyneuropathy

N. Gouider-Khouja, M. Dabbeche, I. Turki, S. Oueslati, N. Miladi, M. Ben Hamida, F. Hentati

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 134 KB

english, 1997

100

Recessive sensory and motor hereditary neuropathy associated with juvenile glaucoma

R. Gouider, T. Dogui, M. Fredj, E. Leguern, S. Ben Ammou, A. Mrabet

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 256 KB

english, 1997