N. Gouider-Khouja: search on Z-Library

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1

Place de la toxine botulique dans le traitement de la spasticité de l’enfant

Benrhouma, H., Yacoubi, J., Kraoua, I., Klaa, H., Ben Youssef-Turki, I., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2014

File:

PDF, 851 KB

2014

2

O - 11 Anémie de Biermer avec un taux normal de la vitamine B12. Importance du dosage de l’homocystéine

Gabsi-Gherairi, S., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2007

Language:

french

File:

PDF, 62 KB

french, 2007

3

Neurophysiological stud/INS;y in infantile neuroaxonal dystrophy: Retrospective review of seventeen North-African patients

Kraoua, I., Romani, M., Benrhouma, H., Klaa, H., Hassen-Rouissi, A., Valente, E.-M., Gouider-Khouja, N., Youssef-Turki, I. Ben

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 60 KB

english, 2013

4

Particularités de la chorée de l’enfant en Tunisie : étude descriptive de 54 cas

Nasri, A., Ben Rhouma, H., Kraoua, I., Klaa, H., Rouissi, A., Turki, I., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2013

Language:

french

File:

PDF, 54 KB

french, 2013

5

Aspects cliniques et thérapeutiques des dystonies en Tunisie : étude prospective sur cinq ans

Benrhouma, H., Kraoua, I., Klaa, H., Rouissi, A., Turki, I., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2013

File:

PDF, 324 KB

2013

6

Place de la médecine nucléaire dans le syndrome de Kinsbourne

Ben Sellem, D., Mahjoub, Y., Rebai, I., Letaief, B., Gouider-Khouja, N., Ben Slimene, M.F.

Journal:

Médecine Nucléaire

Year:

2013

Language:

french

File:

PDF, 50 KB

french, 2013

7

Eye movements in parkinsonian syndromes

Marie Vidailhet, Sophie Rivaud, Neziha Gouider-Khouja, Bernard Pillon, Anne-Marie Bonnet, Bertrand Gaymard, Yves Agid, Pr. Charles Pierrot-Deseilligny

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 676 KB

english, 1994

8

Reply

M. Vidailhet, S. Rivaud, N. Gouider-Khouja, B. Pillon, A. M. Bonnet, B. Gaymard, Y. Agid, C. Pierrot-Deseilligny

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 247 KB

english, 1994

9

“Pure” striatonigral degeneration and Parkinson's disease: A comparative clinical study

Dr. Neziha Gouider-Khouja, Marie Vidailhet, Anne-Marie Bonnet, Jacques Pichon, Yves Agid

Journal:

Movement Disorders

Year:

1995

Language:

english

File:

PDF, 636 KB

english, 1995

10

Urinary disturbances in striatonigral degeneration and parkinson's disease: Clinical and urodynamic aspects

Dr. A. M. Bonnet, J. Pichon, M. Vidailhet, N. Gouider-Khouja, G. Robain, M. Perrigot, Y. Agid

Journal:

Movement Disorders

Year:

1997

Language:

english

File:

PDF, 445 KB

english, 1997

11

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

12

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

13

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

14

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

15

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

16

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

17

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

18

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

19

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

20

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

21

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

22

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

23

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

24

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

25

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

26

O.034 Wilson's disease

N. Gouider-Khouja

Journal:

Parkinsonism & Related Disorders

Year:

2009

Language:

english

File:

PDF, 57 KB

english, 2009

27

Wilson's disease

Neziha Gouider-Khouja

Journal:

Parkinsonism & Related Disorders

Year:

2009

Language:

english

File:

PDF, 111 KB

english, 2009

28

275 EFFECT OF EARLY BOTULINUM TOXIN TREATMENT OF SPASTIC GAIT IN CEREBRAL PALSY: A 10 YEAR FOLLOW-UP STUDY

N. Gouider-Khouja, H. Benrhouma, N. Fraj

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 48 KB

english, 2010

29

Hemiparkinsonian syndrome due to a cerebral tumor infiltrating the substantia nigra

N Gouider-Khouja, S Gabsi, N Khouja, F Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2000

Language:

english

File:

PDF, 876 KB

english, 2000

30

Intrafamilial phenotypic variability of Hallervorden–Spätz syndrome in a Tunisian family

N Gouider-Khouja, N Miladi, S Belal, F Hentati

Journal:

Parkinsonism & Related Disorders

Year:

2000

Language:

english

File:

PDF, 380 KB

english, 2000

31

PO17-TU-14 Diagnosis of mitochondriopathies in Tunisia

I. Kraoua, H. Benrhouma, I. Marouani, S. Hamdi, N. Fradj, A. Rouissi, S. Zekri, N. Kaabachi, M. Jaafoura, N. Gouider-Khouja

Journal:

Journal of the Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 45 KB

english, 2009

32

PO17-TU-12 A Tunisian family with succinate dehydrogenase deficiency presenting with leucodystrophy associated to polydactyly

I. Kraoua, S. Hamdi, H. Benrhouma, N. Fradj, A. Rouissi, K. Tlili, N. Gouider-Khouja

Journal:

Journal of the Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 44 KB

english, 2009

33

Ãtude comparative des aspects cliniques et paracliniques de la sclÃ©rose en plaques en Tunisie

Ammar, N., Gouider-Khouja, N., Hentati, F.

Journal:

Revue Neurologique

Year:

2006

File:

PDF, 310 KB

2006

34

Diagnostic et prise en charge des maladies neuromÃ©taboliques en Tunisie. Ãtude prospective sur trois ans

Kraoua, I., Benrhouma, H., Rouissi, A., Youssef-Turki, I. Ben, Zouari, B., Kaabachi, N., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2009

Language:

english

File:

PDF, 192 KB

english, 2009

35

Encéphalite rubéolique : observation récente d’une fréquence inhabituelle

Ben Achour, N., Benrhouma, H., Rouissi, A., Touaiti, H., Kraoua, I., Turki, I., Gouider-Khouja, N.

Journal:

Archives de Pédiatrie

Year:

2013

File:

PDF, 247 KB

2013

36

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

Rebai, Ibtihel, Ben Rhouma, Hanene, Kraoua, Ichraf, Klaa, Hedia, Rouissi, Aida, Ben Youssef-Turki, Ilhem, Gouider-Khouja, Neziha

Journal:

Brain and Development

Year:

2015

Language:

english

File:

PDF, 1.04 MB

english, 2015

37

Le signe de « la dent molaire » dans l'ataxie—apraxie oculomotrice

Nagi, S., Boudabbous, S., Sebaï, R., Kraoua, I., Turki, I., Gouider-Khouja, N., Ben Hamouda, M.

Journal:

Journal of Neuroradiology

Year:

2007

Language:

french

File:

PDF, 100 KB

french, 2007

38

Sténose bilatérale non tumorale des foramens de Monro

Hammami, N., Boughanmi, N., Drissi, C., Kerkeni, A., Kallel, J., Jemel, H., Gouider-Khouja, N., Nagi, S., Ben Hamouda, M.

Journal:

Journal of Neuroradiology

Year:

2011

File:

PDF, 177 KB

2011

39

Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child

Rebai, Ibtihel, Kraoua, Ichraf, Benrhouma, Hanene, Rouissi, Aida, Turki, Ilhem, Ceballos-Picot, Irène, Gouider-Khouja, Neziha

Journal:

Brain and Development

Year:

2014

Language:

english

File:

PDF, 270 KB

english, 2014

40

Les leucoencéphalopathies d’origine génétique : aspects cliniques et neuroradiologiques

Rébai, I., Ichraf, K., Benrhouma, H., Klaa, H., Boesflug-Tanguy, O., Gouider-Khouja, N., Ben Youssef-Turki, I.

Journal:

Revue Neurologique

Year:

2014

File:

PDF, 193 KB

2014

41

Étude d’épidémiologie génétique des dystonies familiales en Tunisie

Benrhouma, H., Gouider-Khouja, N., Sheerin, U., Charlesworth, G., Turki, I., Wood, N.

Journal:

Revue Neurologique

Year:

2014

Language:

french

File:

PDF, 419 KB

french, 2014

42

Impact des mutations de la dystrophine sur le profil cognitif des patients atteints de dystrophie musculaire de Duchenne

Ben Achour, N., Kraoua, I., Benrhouma, H., Klaa, H., Hassen, A., Gouider-Khouja, N., Ben Youssef-Turki, I.

Journal:

Revue Neurologique

Year:

2014

Language:

french

File:

PDF, 191 KB

french, 2014

43

Nécrose élective de la substance noire au cours du neuropaludisme

Nagi, S., Rebaï, I., Rouissi, A., Hammami, N., Ben Rhouma, H., Drissi, C., Gouider-Khouja, N., Ben Hamouda, M.

Journal:

Journal of Neuroradiology

Year:

2012

Language:

french

File:

PDF, 42 KB

french, 2012

44

Maladie de Pelizaeus-Merzbacher-like : aspects clinico-radiologiques

Rébai, I., Drissi, C., Kraoua, I., Dorboz, I., Benrhouma, H., Klaa, H., Rouissi, A., Ben Mohamed, M., Boesflug-Tanguy, O., Gouider-Khouja, N., Ben Youssef-Turki, I.

Journal:

Journal of Neuroradiology

Year:

2014

Language:

french

File:

PDF, 54 KB

french, 2014

45

Management of muscular dystrophies in Tunisian children

Achour, N. Ben, Kraoua, I., Benrhouma, H., Klaa, H., Rouissi, A., Gouider-Khouja, N., Youssef-Turki, I. Ben

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 73 KB

english, 2013

46

Profils neuropsychologiques des dystrophies musculaires progressives

Ben Achour, N., Klaa, H., Benrhouma, H., Kraoua, I., Rouissi, A., Turki, I., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2013

Language:

french

File:

PDF, 52 KB

french, 2013

47

Un CMT1A génétiquement confirmée mimant une CIDP à rechute

Ben Youssef-Turki, I., Kraoua, I., Gargouri, A., Bouche, P., Leguern, E., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2011

File:

PDF, 84 KB

2011

48

Particularités des urgences en mouvements anormaux de l’enfant

Benrhouma, H., Touaiti, H., Ben Achour, N., Klaa, H., Kraoua, I., Turki, I., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2013

Language:

french

File:

PDF, 174 KB

french, 2013

49

Paralysie du regard latéral et scoliose progressive : à propos de 4 familles tunisiennes

El Bahri-Ben Mrad, F., Gouider-Khouja, N., Gabsi, S., Larnaout, A., Boughammoura, A., Kefi, M., Belal, S., Hentati, F.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 93 KB

french, 2004

50

Syndromes neurologiques paranéoplasiques de l’enfant

Youssef-Turki, Ilhem Ben, Ben Achour, Nadia, Touati, Hajer, Kraoua, Ichraf, Benrhouma, Hanene, Rouissi, Aida, Gouider-Khouja, Neziha

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 64 KB

french, 2012