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

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

3

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

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

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

6

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

7

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

8

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

9

Cognitive and psychological profile in Tunisian children with Duchenne muscular dystrophy

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

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 57 KB

english, 2013

10

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

11

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

12

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

13

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

14

O.034 Wilson's disease

N. Gouider-Khouja

Journal:

Parkinsonism & Related Disorders

Year:

2009

Language:

english

File:

PDF, 57 KB

english, 2009

15

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

16

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

17

PO26-TH-04 Impact of a systematic protocol of management of progressive muscular dystrophy on disease parameters: a study of 45 cases over 5 years

Smirani, S., Gabsi-Gherairi, S., Fredj, N., Rouissi, A., Gouider-Khouja, N.

Journal:

Journal of the Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 45 KB

english, 2009

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

Clinical and genetic aspects of autosomal recessive forms of Parkinson's disease

Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2012

File:

PDF, 138 KB

2012

20

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

21

Brain imaging in chorea in Tunisian children

Nasri, A., Benrhouma, H., Rebai, I., Kraoua, I., Drissi, C., Klaa, H., Achour, N. Ben, Rouissi, A., Gouider-Khouja, N., Hammouda, M. Ben, Turki, I.

Journal:

Journal of the Neurological Sciences

Year:

2013

Language:

english

File:

PDF, 80 KB

english, 2013

22

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

23

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

24

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

25

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation

Ghorbel, Rania, Ghorbel, Raouia, Rouissi, Aida, Fendri-Kriaa, Nourhene, Ben Salah, Ghada, Belguith, Neila, Ammar-Keskes, Leila, Gouider-Khouja, Neziha, Fakhfakh, Faiza

Journal:

Biochemical and Biophysical Research Communications

Year:

2018

Language:

english

File:

PDF, 1.77 MB

english, 2018

26

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

27

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

28

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

29

Urinary Disturbances in Striatonigral Degeneration and Parkinson's Disease: Clinical and Urodynamic Aspects

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

Journal:

The Journal of Urology

Year:

1999

Language:

english

File:

PDF, 112 KB

english, 1999

30

Infantile and childhood onset PLA2G6 -associated neurodegeneration in a large North African cohort

Romani, M., Kraoua, I., Micalizzi, A., Klaa, H., Benrhouma, H., Drissi, C., Turki, I., Castellana, S., Mazza, T., Valente, E. M., Gouider-Khouja, N.

Journal:

European Journal of Neurology

Year:

2015

Language:

english

File:

PDF, 480 KB

english, 2015

31

Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6 -associated neurodegeneration

Kraoua, I., Romani, M., Tonduti, D., BenRhouma, H., Zorzi, G., Zibordi, F., Ardissone, A., Gouider-Khouja, N., Ben Youssef-Turki, I., Nardocci, N., Valente, E. M.

Journal:

European Journal of Neurology

Year:

2016

Language:

english

File:

PDF, 309 KB

english, 2016

32

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

33

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

34

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

35

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

36

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

37

Seronegative myasthenia gravis with bladder dysfunction

Kraoua, I., BenRhouma, H., Rebai, I., Rouissi, A., Koubaa, S., Turki, I., Dziri, C., Gouider-Khouja, N., Marouani, I.

Journal:

Revue Neurologique

Year:

2012

Language:

english

File:

PDF, 118 KB

english, 2012

38

Chorée aiguë après encéphalite herpétique : réplication virale ou mécanisme immunologique ?

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

Journal:

Archives de Pédiatrie

Year:

2015

File:

PDF, 587 KB

2015

39

Reply to Dr. Suresh Kumar

Ichraf, Kraoua, Neziha, Gouider-Khouja

Journal:

Brain and Development

Year:

2013

Language:

english

File:

PDF, 48 KB

english, 2013

40

Une sténose congénitale des foramens interventriculaires révélée par une hypertension intracrânienne à rechute

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

Journal:

Year:

2013

Language:

french

File:

PDF, 589 KB

french, 2013

41

[IEEE 2012 11th International Conference on Information Sciences, Signal Processing and their Applications (ISSPA) - Montreal, QC, Canada (2012.07.2-2012.07.5)] 2012 11th International Conference on Information Science, Signal Processing and their Applications (ISSPA) - Arabic adaptation of Phonology and Memory test using entropy-based analysis of word complexity

Bacha, Sofiene, Ghozi, Raja, Jaidane, Meriem, Gouider-Khouja, Neziha

Year:

2012

Language:

english

File:

PDF, 486 KB

english, 2012

42

Neuropsychological pattern of striatonigral degeneration: comparison with Parkinson's disease and progressive supranuclear palsy.

Pillon, B, Gouider-Khouja, N, Deweer, B, Vidailhet, M, Malapani, C, Dubois, B, Agid, Y

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

1995

Language:

english

File:

PDF, 1.21 MB

english, 1995

43

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

44

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

45

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

46

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

47

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

48

Tuberculose cérébromédiastinale chez un enfant atteint de syndrome de Say-Barber-Miller probable : un lien de causalité ?

Kechaou, I., Rouissi, A., Kraoua, I., Regayeg, A., Turki, I., Ben Hamouda, M., Gouider-Khouja, N.

Journal:

Revue Neurologique

Year:

2009

Language:

english

File:

PDF, 351 KB

english, 2009

49

Encéphalite rubéolique : observation récente d’une fréquence inhabituelle

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

Journal:

Revue Neurologique

Year:

2012

Language:

french

File:

PDF, 62 KB

french, 2012

50

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

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