T Chkili: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Exchange rate movements and stock market returns in a regime-switching environment: Evidence for BRICS countries

Chkili, Walid, Nguyen, Duc Khuong

Journal:

Research in International Business and Finance

Year:

2014

Language:

english

File:

PDF, 768 KB

english, 2014

2

Régression spontanée d’une hernie discale lombaire : « une hernie fantôme » à propos de trois cas et revue de la littérature

Mezghani, N., Choura, S.A., Ammar, H., Radhouane, K., Chkili, R.

Journal:

Year:

2018

Language:

french

File:

PDF, 294 KB

french, 2018

3

Volatility forecasting and risk management for commodity markets in the presence of asymmetry and long memory

Chkili, Walid, Hammoudeh, Shawkat, Nguyen, Duc Khuong

Journal:

Energy Economics

Year:

2014

Language:

english

File:

PDF, 807 KB

english, 2014

4

Agraphie pure en arabe : dissociation entre voyelles et consonnes syndrome du buffer graphémique

El Alaoui Faris, M., Benbelaid, F., Ettahiri, L., Jiddane, M., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

File:

PDF, 56 KB

2004

5

Kyste synovial hémorragique : une cause rare de compression médullaire cervicale

Radhouane, K., Achoura, S., Harbaoui, A., Ammar, H., Yedeas, M., Chkili, R.

Journal:

Year:

2018

Language:

french

File:

PDF, 236 KB

french, 2018

6

Asymmetric effects and long memory in dynamic volatility relationships between stock returns and exchange rates

Walid Chkili, Chaker Aloui, Duc Khuong Nguyen

Journal:

Journal of International Financial Markets, Institutions and Money

Year:

2012

Language:

english

File:

PDF, 635 KB

english, 2012

7

Dynamic correlations and hedging effectiveness between gold and stock markets: evidence for BRICS countries

Journal:

Research in International Business and Finance

Year:

2016

Language:

english

File:

PDF, 954 KB

english, 2016

8

Le mutisme cérébelleux « entité rare ou sous-estimée »

Radhouane, K., Achoura, S., Harbaoui, A., Ammar, H., Yedeas, M., Chkili, R.

Journal:

Year:

2018

Language:

french

File:

PDF, 364 KB

french, 2018

9

Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I

Dr. A. Benomar, E. Le Guern, A. Dürr, H. Ouhabi, G. Stevanin, M. Yahyaoui, T. Chkili, Y. Agid, A. Brice

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 532 KB

english, 1994

10

Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene

Pierre Labauge, RÉDa Ouazzani, Amel M'Rabet, Djamel Grid, Pierre Genton, Charlotte Dravet, Taieb Chkili, Corrine Beck, Catherine Buresi, Michel Baldy-Moulinier, Dr Alain Malafosse

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 414 KB

english, 1997

11

Mal de Pott sous-occipital : trois cas

Fadoua Allali, Ali Benomar, Mohamed El Yahyaoui, Taib Chkili, Najia Hajjaj-Hassouni

Journal:

Revue du Rhumatisme

Year:

2000

Language:

french

File:

PDF, 881 KB

french, 2000

12

High incidence of SMN1 gene deletion in Moroccan adult-onset spinal muscular atrophy patients

A. Bouhouche, A. Benomar, N. Birouk, N. Bouslam, R. Ouazzani, M. Yahyaoui, T. Chkili

Journal:

Journal of Neurology

Year:

2003

Language:

english

File:

PDF, 215 KB

english, 2003

13

Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31–14.1

Bouhouche, Ahmed, Benomar, Ali, Bouslam, Naima, Ouazzani, Reda, Chkili, Taïeb, Yahyaoui, Mohamed

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 88 KB

english, 2005

14

Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations

A. Benomar, F. Meggouh, O. Didierjean, N. Kissani, A. Dürr, A. Sefiani, T. Chkili, Y. Agid, M. Yahyaoui, A. Brice

Journal:

European Journal of Neurology

Year:

1996

Language:

english

File:

PDF, 256 KB

english, 1996

15

Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients

Naima Marzouki, Ali Benomar, Mohamed Yahyaoui, Nezha Birouk, Mohamed Elouazzani, Taib Chkili, Mohamed Benlemlih

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 208 KB

english, 2005

16

Stock market volatility and exchange rates in emerging countries: A Markov-state switching approach

Chkili Walid, Aloui Chaker, Omar Masood, John Fry

Journal:

Emerging Markets Review

Year:

2011

Language:

english

File:

PDF, 760 KB

english, 2011

17

Myélite isolée et maladie de Behçet : trois observations

H Harmouche, O Mouti, M El-Alaoui Faris, S Aidi, M Benabdeljalil, T Chkili

Journal:

La Revue de Médecine Interne

Year:

2000

Language:

french

File:

PDF, 941 KB

french, 2000

18

La maladie de Wilson: étude de 21 cas

W. Bono, O. Moutie, S. Aïdi, A. Benomar, M. Benabdejlil, M. Alaoui-Faris, M. Yahyaoui, T. Chkili

Journal:

La Revue de Médecine Interne

Year:

1999

File:

PDF, 173 KB

1999

19

La maladie de Wilson. Étude clinique, thérapeutique et évolutive de 21 cas

W. Bono, O. Moutie, A. Benomar, S. Aïdi, M. El Alaoui-Faris, M. Yahyaoui, T. Chkili

Journal:

La Revue de Médecine Interne

Year:

2002

File:

PDF, 148 KB

2002

20

Infarctus cérébral, syndrome pseudolupique et myxome de l'oreillette gauche

K Benbouazza, M El Alaoui Faris, A Benomar, Z Chefchaouni, A Amarti, O Fennich, S Ztot, A Slaoui, R El Hassani, T Chkili

Journal:

La Revue de Médecine Interne

Year:

1997

File:

PDF, 468 KB

1997

21

The axonal form of autosomal recessive Charcot-Marie-Tooth (CMT) disease: a phenotype study of 4 Moroccan families

N. Birouk, H. Belaidi, A. Benomar, A. Bouhouche, B. Kably, R. Ouazzani, M. Yahyaoui, E. Le Guern, T. Chkili

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 130 KB

english, 1997

22

Clinical and genetical aspects of autosomal dominant cerebellar ataxia in Morocco (about 16 families)

A. Benomar, M. Yahyaoui, P. Meggouh, N. Bouslam, A. Bouhouche, T Chkili

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 129 KB

english, 1997

23

Crises épileptiques et épilepsie dans le cadre d’une panencéphalite sclérosante subaiguë (à propos de 30 cas)

N Kissani, R Ouazzani, H Belaidi, H Ouahabi, T Chkili

Journal:

Neurophysiologie Clinique/Clinical Neurophysiology

Year:

2001

File:

PDF, 229 KB

2001

24

A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset

Maria D. Lalioti, Hamish S. Scott, Pierre Genton, Djamel Grid, Réda Ouazzani, Amel M'Rabet, Sadi Ibrahim, Riadh Gouider, Charlotte Dravet, Taieb Chkili, Armand Bottani, Catherine Buresi, Alain Malafos

Journal:

The American Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 265 KB

english, 1998

25

A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3

Ahmed Bouhouche, Ali Benomar, Nazha Birouk, Angélique Mularoni, Farid Meggouh, Johann Tassin, Djamal Grid, Antoon Vandenberghe, Mohamed Yahyaoui, Taïeb Chkili, Alexis Brice, Eric LeGuern

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 423 KB

english, 1999

26

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

H. Azzedine, A. Bolino, T. Taïeb, N. Birouk, M. Di Duca, A. Bouhouche, S. Benamou, A. Mrabet, T. Hammadouche, T. Chkili, R. Gouider, R. Ravazzolo, A. Brice, J. Laporte, E. LeGuern

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 1.43 MB

english, 2003

27

Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families

Ali Benomar, Mohammed Yahyaoui, Farid Meggouh, Ahmed Bouhouche, Mohammed Boutchich, Naima Bouslam, Abdelhaq Zaim, Michèle Schmitt, Halima Belaidi, Reda Ouazzani, Taı̈b Chkili, Michel Koenig

Journal:

Journal of the Neurological Sciences

Year:

2002

Language:

english

File:

PDF, 91 KB

english, 2002

28

PO07-MO-04 Miliary brain tuberculomas: a case report

I. Kacem, M. Ben Ammar, N. Ben Ali, R. Chkili, J. Zaouali, R. Mrissa, M. Yedaes

Journal:

Journal of the Neurological Sciences

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

29

1-29-02 Correlation between clinical and genetical data of Freidriech ataxia and ataxia with vitamin E deficiency

A. Benomar, F. Meggouh, L. Reutnaner, M. Boutchich, A. Zaǐm, M. Schmitt, A. Bouhouche, J.J. Belaǐdi, R. Ouazani, M. Yahyaoui, T. Chkili, M. Koenig

Journal:

Journal of the Neurological Sciences

Year:

1997

Language:

english

File:

PDF, 178 KB

english, 1997

30

Vitamin E deficiency ataxia associated with adenoma

Ali Benomar, Mohammed Yahyaoui, Naima Marzouki, Nezha Birouk, Naima Bouslam, Halima Belaidi, Afaf Amarti, Reda Ouazzani, Taieb Chkili

Journal:

Journal of the Neurological Sciences

Year:

1999

Language:

english

File:

PDF, 567 KB

english, 1999

31

Behçet's disease in Moroccan children: a report of 12 cases

Allali, F, Benomar, A, Karim, A, Lazrak, N, Mohcine, Z, El Yahyaoui, M, Chkili, T, Hajjaj‐Hassouni, N

Journal:

Scandinavian Journal of Rheumatology

Year:

2004

Language:

english

File:

PDF, 168 KB

english, 2004

32

Ãtude clinique et electrophysiologique de 180 cas de syndrome de Guillain-BarrÃ©

Birouk, N., Berramdane, M., Belaidi, H., Kably, B., El Alaoui Faris, M., Yahyaoui, M., Ouazzani, R., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 47 KB

french, 2004

33

Les dystrophies musculaires (DM) des ceintures : étude clinique et immunohistochimique (IHC) de 120 familles marocaines

Birouk, N., Amarti, A., Kably, B., Belaïdi, H., Sefiani, S., Yahyaoui, M., Ouazzani, R., Saïdi, A., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 55 KB

french, 2004

34

Syndrome catatonique traité par zolpidem et bromocriptine quatre observations

Benabdeljlil, M., El Alaoui Faris, M., Douira, L., Aïdi, S., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

File:

PDF, 52 KB

2004

35

Maladie d’Alzheimer et autres démences au Maroc Expérience d’un centre de la mémoire à partir de l’étude prospective de 160 cas

Benabdeljlil, M., El Alaoui Faris, M., Aïdi, S., Boutbibe, F., Benbelaïd, F., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 62 KB

french, 2004

36

Polyradiculonévrites chroniques : étude clinique, électrophysiologique et évolutive de 24 cas

Belaidi, H., Benaaboud, B., Birouk, N., Kably, B., Aidi, S., El Alaoui Faris, M., Yahyaoui, M., Ouazzani, R., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 47 KB

french, 2004

37

Troubles cognitifs dus à l’intoxication oxycarbonée: étude neuropsychologique et IRM de 5 cas

Rahmani, M., Bennani, M., Benabdeljlil, M., Aidi, S., Jiddane, M., Chkili, T., El Alaoui Faris, M.

Journal:

Revue Neurologique

Year:

2006

File:

PDF, 372 KB

2006

38

L’encephalite de Bickerstaff : étude de 4 cas

Hassani, R., Seddiki, F.Z., Benaboud, B., Benabdeljlil, M., Aïdi, S., Jiddane, M., Boukhrissi, N., El Alaoui-Faris, M., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

File:

PDF, 53 KB

2004

39

Syndrome SLA révélant une thyroïdite de Hashimoto : à propos de 2 cas

Benaaboud, B., Hassani, R., Aïdi, S., Benabdeljlil, M., Farouki, Z., Birouk, N., Slassi, I., El Alaoui Faris, M., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

File:

PDF, 64 KB

2004

40

Forme axonale de la maladie de Charcot-Marie-Tooth autosomique récessive (ARCMT2) : corrélations phénotype-génotype chez 13 familles marocaines

Bouhouche, A., Birouk, N., Azzedine, H., Benomar, A., Bouslam, N., Ouazzani, R., Leguern, E., Yahyaoui, M., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 54 KB

french, 2004

41

Hypertension intracrânienne bénigne

Errguig, L., Benomar, A., Aitbenhaddou, E., Mouti, O., Regragui, W., Benaaboud, B., Yahyaoui, M., Chkili, T.

Journal:

Revue Neurologique

Year:

2004

File:

PDF, 76 KB

2004

42

Instabilities in the relationships and hedging strategies between crude oil and US stock markets: Do long memory and asymmetry matter?

Chkili, Walid, Aloui, Chaker, Nguyen, Duc Khuong

Journal:

Journal of International Financial Markets, Institutions and Money

Year:

2014

Language:

english

File:

PDF, 553 KB

english, 2014

43

Apport de l’ostéodensitométrie par ultrasons dans le diagnostic de l’ostéoporose : étude prospective de 368 cas

Ben Abdelghani, K., Dhahri, R., Souabni, L., Jammali, S., Kassab, S., Chkili, S., Laatr, A., Zakraoui, L.

Journal:

La Revue de Médecine Interne

Year:

2014

Language:

french

File:

PDF, 58 KB

french, 2014

44

Establishment of T-Lymphoid Cell Lines from Morroccan Patients with Tropical Spastic Paraparesis

FAROUQI, B., YAHYAOUI, M., ALAOUI, F.M., NORAZ, N., SEKKAT, S., CHKILI, T., DESGRANGES, C., BENSLIMANE, A.

Journal:

AIDS Research and Human Retroviruses

Year:

1992

Language:

english

File:

PDF, 2.39 MB

english, 1992

45

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

Meggouh, F, Benomar, A, Rouger, H, Tardieu, S, Birouk, N, Tassin, J, Barhoumi, C, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E

Journal:

Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 515 KB

english, 1998

46

Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene

Birouk, Nazha, Azzedine, Hamid, Dubourg, Odile, Muriel, Marie-Paule, Benomar, Ali, Hamadouche, Tarik, Maisonobe, Thierry, Ouazzani, Reda, Brice, Alexis, Yahyaoui, Mohamed, Chkili, Taïb, Le Guern, Eric

Journal:

Archives of Neurology

Year:

2003

Language:

english

File:

PDF, 256 KB

english, 2003

47

A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families

Bouhouche, Ahmed, Birouk, Nazha, Benomar, Ali, Ouazzani, Reda, Chkili, Taïeb, Yahyaoui, Mohamed

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2007

File:

PDF, 158 KB

2007

48

Middle cerebral artery occlusion due to hydatid cysts of myocardial and intraventricular cavity cardiac origin. Two cases

Benomar, A., Yahyaoui, M., Birouk, N., Vidailhet, M., Chkili, T.

Journal:

Year:

1994

Language:

english

File:

PDF, 718 KB

english, 1994

49

AB0187 Influence of Educational Level on The Outcomes of Rheumatoid Arthritis

Essafi, F., Fazaa, A., Kchaou, S., Ben Abdelghani, K., Kassab, S., Chkili, S., Laatar, A., Zakraoui, L.

Journal:

Annals of the Rheumatic Diseases

Year:

2016

Language:

english

File:

PDF, 91 KB

english, 2016

50

AB0237 Joints count in rheumatoid arthritis: a correlation study between 3 clinicians and ultrasound joints count and the impact on disease activity

Ben Abdelghani, K., Dridi, L., Souabni, L., Fazaa, A., Kassab, S., Chkili, S., Laatar, A., Zakraoui, L.

Journal:

Annals of the Rheumatic Diseases

Year:

2013

Language:

english

File:

PDF, 219 KB

english, 2013