I. Kraoua: search on Z-Library

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1

Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review

Ben Achour, Nedia, Ben Younes, Thouraya, Rebai, Ibtihel, Ben Ahmed, Melika, Kraoua, Ichraf, Ben Youssef –Turki, Ilhem

Journal:

European Journal of Paediatric Neurology

Year:

2018

Language:

english

File:

PDF, 580 KB

english, 2018

2

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

3

Encéphalopathies épileptiques génétiques du nourrisson

Ziada, Sabrine, Klaa, Hedia, Younes, Thouraya Ben, Benrhouma, Hanene, Rouissi, Aida, Kraoua, Ichraf, Youssef-Turki, Ilhem Ben

Journal:

Revue Neurologique

Year:

2019

Language:

french

File:

PDF, 166 KB

french, 2019

4

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

5

Myasthénie auto-immune juvénile

Ben Younes, Thouraya, Klaa, Hedia, Ben Achour, Nadia, Benrhouma, Hanene, Rouissi, Aida, Kraoua, Ichraf, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2016

Language:

french

File:

PDF, 66 KB

french, 2016

6

Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young; Seltene Multiallelvarianten sprechen für einen oligogenen Ursprung des plötzlichen Herztods bei jungen Menschen;

Jaouadi, Hager, Bouyacoub, Yosra, Chabrak, Sonia, Kraoua, Lilia, Zaroui, Amira, Elouej, Sahar, Nagara, Majdi, Dallali, Hamza, Delague, Valérie, Levy, Nicolas, Benkhalifa, Rym, Mechmeche, Rachid, Zaffr

Journal:

Year:

2020

Language:

english

File:

PDF, 612 KB

english, 2020

7

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

8

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

9

Mutations inB9D1andMKS1cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Romani, Marta, Micalizzi, Alessia, Kraoua, Ichraf, Dotti, Maria, Cavallin, Mara, Sztriha, László, Ruta, Rosario, Mancini, Francesca, Mazza, Tommaso, Castellana, Stefano, Hanene, Benrhouma, Carluccio,

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 564 KB

english, 2014

10

Ophtalmoplégie douloureuse récidivante : migraine ophtalmoplégique ou schwannome du nerf oculomoteur ?

Riahi, A., Ben Youssef-Turki, I., Walha, K., Kraoua, I., Benrhouma, H., Klaa, H., Rouissi, A.

Journal:

Pratique Neurologique - FMC

Year:

2014

File:

PDF, 820 KB

2014

11

Enraidissement musculaire et crampes chez un enfant : penser au syndrome de Brody

Ben Achour, N., Kessentini, N., Kraoua, I., Ben Youssef-Turki, I.

Journal:

Archives de Pédiatrie

Year:

2015

File:

PDF, 125 KB

2015

12

Encéphalomyélite aiguë disséminée en Tunisie : étude d’une cohorte pédiatrique

Ben Achour, N., Ben Waddey, O., Kraoua, I., Benrhouma, H., Klaa, H., Rouissi, A., Ben Youssef-Turki, I.

Journal:

Revue Neurologique

Year:

2015

File:

PDF, 766 KB

2015

13

Hypertension intracrânienne de l’enfant

Younes, Thouraya Ben, Naas, Amira, Klaa, Hedia, Benrhouma, Hanene, Achour, Nadia Ben, Kraoua, Ichraf, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2016

Language:

french

File:

PDF, 53 KB

french, 2016

14

Les caractéristiques des mouvements anormaux dans le déficit en neurotransmetteurs

Kessentini, Nahed, Kraoua, Ichraf, Benrhouma, Hanene, Klaa, Hedia, Achour, Nedia Ben, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2016

Language:

french

File:

PDF, 54 KB

french, 2016

15

Encéphalites limbiques auto-immunes de l’enfant en Tunisie

Ben Achour, Nedia, Mhiri, Mariem, Klaa, Hedia, Benrhouma, Hanene, Rouissi, Aida, Kraoua, Ichraf, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2016

Language:

french

File:

PDF, 66 KB

french, 2016

16

Épilepsie auto-immune chez l’enfant

Makhlouf, Sinda, Klaa, Hedia, Benrhouma, Hanene, Achour, Nedia Ben, Rouissi, Aida, Kraoua, Ichraf, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2017

Language:

french

File:

PDF, 78 KB

french, 2017

17

Comment on ‘Acute flaccid myelitis in childhood: a retrospective cohort study’

Ben Achour, N., Jeridi, C., Rebai, I., Nagi, S., Kraoua, I., Ben Youssef -Turki, I.

Journal:

European Journal of Neurology

Year:

2017

Language:

english

File:

PDF, 384 KB

english, 2017

18

Ataxie télangiectasie de l’enfant

Klaa, Hedia, Benrhouma, Hanene, Rouissi, Aida, Kraoua, Ichraf, Turki, Ilhem

Journal:

Revue Neurologique

Year:

2018

Language:

french

File:

PDF, 166 KB

french, 2018

19

Syndrome de Leigh : étude clinique, radiologique et génétique d’une série tunisienne

Zioudi, Abir, Kraoua, Ichraf, Klaa, Hedia, Younes, Thouraya Ben, Rouissi, Aida, Benrhouma, Hanene, Youssef-Turki, Ilhem Ben

Journal:

Revue Neurologique

Year:

2019

Language:

french

File:

PDF, 167 KB

french, 2019

20

Hémiatrophie cérébrale : approche clinico-radiologique

Younes, Thouraya Ben, Kraoua, Ichraf, Drissi, Cyrine, Klaa, Hedia, Rouissi, Aida, Benrhouma, Hanene, Youssef-Turki, Ilhem Ben

Journal:

Revue Neurologique

Year:

2019

Language:

french

File:

PDF, 227 KB

french, 2019

21

Neurodégénérescence associée à un déficit en Pantothénate-kinase-2

Jemai, Khaoula, Benrhouma, Hanene, Klaa, Hedia, Younes, Thouraya Ben, Rouissi, Aida, Kraoua, Ichraf, Youssef-Turki, Ilhem Ben

Journal:

Revue Neurologique

Year:

2019

Language:

french

File:

PDF, 172 KB

french, 2019

22

A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigree

L. Abaied, M. Trabelsi, M. Chaabouni, M. Kharrat, L. Kraoua, R. M'rad, N. Tebib, F. Maazoul, H. Chaabouni

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 161 KB

english, 2010

23

Germinal mosaicism in Noonan syndrome: A family with two affected siblings of normal parents

Siham Chafai Elalaoui, Lilia Kraoua, Céline Liger, Ilham Ratbi, Hélène Cavé, Abdelaziz Sefiani

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 130 KB

english, 2010

24

Parkinsonism in Gaucher's disease type 1: Ten new cases and a review of the literature

Ichraf Kraoua, Jérôme Stirnemann, Maria João Ribeiro, Tiphaine Rouaud, Marc Verin, Agnès Annic, Christian Rose, Luc Defebvre, Liliane Réménieras, Michaël Schüpbach, Nadia Belmatoug, Marie Vidailhet, F

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 816 KB

english, 2009

25

FOXL2 mutations in Tunisian patients with blepharophimosis–ptosis–epicanthus inversus syndrome

L Kraoua, M Chaabouni, M Trabelsi, I Chelly, F Maazoul, N Ben Abdallah, S Boukthir, S Barsaoui, H Chaabouni, R M’rad

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 503 KB

english, 2010

26

Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V

M Kharrat, S Trabelsi, M Chaabouni, F Maazoul, L Kraoua, L Ben Jemaa, N Gandoura, S Barsaoui, Y Morel, R M’rad, H Chaabouni

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 597 KB

english, 2010

27

Pseudoaminopterin syndrome

Lilia Kraoua, Yline Capri, Laurence Perrin, Abdelmajjid Benmansour, Alain Verloes

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 6.40 MB

english, 2012

28

A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients

Ichraf Kraoua, Frédéric Sedel, Catherine Caillaud, Roseline Froissart, Jérôme Stirnemann, Guy Chaurand, Hugues Flodrops, Saliha Tari, Isabelle Gourfinkel-An, Sophie Mathieu, Nadia Belmatoug, Thierry B

Journal:

Brain and Development

Year:

2011

Language:

english

File:

PDF, 138 KB

english, 2011

29

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

30

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

31

Constitutional NRAS mutations are rare among patients with Noonan syndrome or juvenile myelomonocytic leukemia

Lilia Kraoua, Hubert Journel, Philippe Bonnet, Jeanne Amiel, Nathalie Pouvreau, Clarisse Baumann, Alain Verloes, Hélène Cavé

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 143 KB

english, 2012

32

A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation

Imen Rejeb, Lamia Ben Jemaa, Leila Abaied, Lilia Kraoua, Yoann Saillour, Faouzi Maazoul, Jamel Chelly, Habiba Chaabouni

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 588 KB

english, 2011

33

Hexasomy of the Prader–Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: Case report

Lilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, Imen Chelly, Ines Ouertani, Lamia Ben Jemaa, Faouzi Maazoul, Thomas Liehr, Habiba Chaabouni

Journal:

European Journal of Medical Genetics

Year:

2011

Language:

english

File:

PDF, 371 KB

english, 2011

34

L’anévrysme de pontage aortocoronaire veineux : une cause rare de masse médiastinale

David Montani, Thierry Wagner, Salah Kraoua, Isabelle Honoré, Jacques Lacronique, Daniel Dusser

Journal:

La Presse Médicale

Year:

2007

Language:

french

File:

PDF, 510 KB

french, 2007

35

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

36

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

37

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

38

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

39

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

40

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

41

Une pleurésie à éosinophiles liée à la prise d’acide valproïque

Bally, C., Martin, C., Kraoua, S., Kanaan, R., Lacronique, J., Dusser, D., Burgel, P.-R.

Journal:

Revue de Pneumologie Clinique

Year:

2011

Language:

french

File:

PDF, 377 KB

french, 2011

42

Analyse génétique du syndrome de Turner : étude tunisienne de 89 cas

Kammoun, I., Chaabouni, M., Trabelsi, M., Ouertani, I., Kraoua, L., Chelly, I., M’rad, R., Ben Jemaa, L., Maâzoul, F., Chaabouni, H.

Journal:

Annales d'Endocrinologie

Year:

2008

File:

PDF, 162 KB

2008

43

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

44

Myélite aiguë de l’enfant révélatrice d’une cryoglobulinémie essentielle

Naas, A., Klaa, H., Kraoua, I., Benrhouma, H., Rouissi, A., Ben Youssef-Turki, I.

Journal:

Revue Neurologique

Year:

2014

File:

PDF, 146 KB

2014

45

Encéphalopathie à POCS révélant une lésion thalamique

Ben Mahmoud, A., Klaa, H., Kraoua, I., Benrhouma, H., Rouissi, A., Ben Youssef-Turki, I.

Journal:

Revue Neurologique

Year:

2014

Language:

french

File:

PDF, 302 KB

french, 2014

46

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

47

Syndrome parkinsonien post-traumatisme crânien sévère

Ben Mahmoud, A., Benrhouma, H., Rebai, I., Kraoua, I., Klaa, H., Turki, I.

Journal:

Revue Neurologique

Year:

2014

Language:

french

File:

PDF, 190 KB

french, 2014

48

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

49

Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy

Trabelsi, Mediha, Chelly, Imen, Maazoul, Faouzi, Chaabouni, Myriam, Ouertani, Ines, Kraoua, Lilia, Khemakhem, Lamia, Mrad, Ridha, Chaabouni, Habiba

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 190 KB

english, 2013

50

Abstracts

Trabelsi, Mediha, Chelly, Imen, Maazoul, Faouzi, Chaabouni, Myriam, Ouertani, Ines, Kraoua, Lilia, Khemakhem, Lamia, Mrad, Ridha, Chaabouni, Habiba

Journal:

Journal of the American Academy of Dermatology

Year:

1986

Language:

english

File:

PDF, 87 KB

english, 1986

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