Hamida, Belal A. : rechercher sur Z-Library

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1

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

Année:

2001

Langue:

english

Fichier:

PDF, 86 KB

english, 2001

2

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria

A. Larnaout, F. Hentati, S. Belal, C. H. Ben Hamida, M. Ben Hamida, N. Kaabachi

Journal:

Acta Neuropathologica

Année:

1994

Langue:

english

Fichier:

PDF, 1.10 MB

english, 1994

3

Familial encephalopathy andl-2-hydroxyglutaric aciduria

N. Kaabachi, A. Larnaout, D. Rabier, C. Jakobs, S. Belal, F. Hentati, P. Parvey, J. Bardet, M. Ben Hamida, A. Mebazaa, P. Kamoun

Journal:

Journal of Inherited Metabolic Disease

Année:

1993

Langue:

english

Fichier:

PDF, 73 KB

english, 1993

4

Friedreich’s ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient

A. Larnaout, S. Belal, M. Zouari, M. Fki, C. Ben Hamida, H. H. Goebel, M. Ben Hamida, F. Hentati

Journal:

Acta Neuropathologica

Année:

1997

Langue:

english

Fichier:

PDF, 463 KB

english, 1997

5

Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings

A. Larnaout, S. Belal, C. Ben Hamida, M. Ben Hamida, F. Hentati

Journal:

Journal of Neurology

Année:

1998

Langue:

english

Fichier:

PDF, 243 KB

english, 1998

6

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1

C.B. Hamida, L. Cavalier, S. Belal, H. Sanhaji, N. Nadal, C. Barhoumi, N. M'Rissa, N. Marzouki, J.-L. Mandel, M.B. Hamida, M. Koenig, F. Hentati

Journal:

Année:

1997

Langue:

english

Fichier:

PDF, 939 KB

english, 1997

7

LINKAGE TO CHROMOSOME 13Q11-12 OF AN AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA IN A TUNISIAN FAMILY

N Mrissa, S Belal, C Ben Hamida, R Amouri, I Turki, R Mrissa, M Ben Hamida, F. Hentati

Journal:

Journal of the Peripheral Nervous System

Année:

2000

Langue:

english

Fichier:

PDF, 179 KB

english, 2000

8

10.1038/81701

Koenig, Michel, Bomont, Pascale, Cavalier, Laurent, Blondeau, François, Hamida, Christiane Ben, Belal, Samir, Tazir, Meriem, Demir, Ercan, Topaloglu, Haluk, Korinthenberg, Rudolf, Tüysüz, Beyhan, Land

Journal:

Nature Genetics

Année:

2000

Langue:

english

Fichier:

PDF, 290 KB

english, 2000

9

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

Ben Hamida, C., Doerflinger, N., Belal, S., Linder, C., Reutenauer, L., Dib, C., Gyapay, G., Vignal, A., Le Paslier, D., Cohen, D.

Journal:

Nature Genetics

Année:

1993

Fichier:

PDF, 803 KB

1993

10

Chromosome 13 liked muscular dystrophy

M.Ben Hamida, C.Ben Hamida, M. Zouari, S. Belal, F. Hentatt

Journal:

Neuromuscular Disorders

Année:

1996

Langue:

english

Fichier:

PDF, 101 KB

english, 1996

11

Limb-girdle muscular dystrophy 2C: Clinical aspects

M. Ben Hamida, Ch. Ben Hamida, M. Zouari, S. Belal, F. Hentati

Journal:

Neuromuscular Disorders

Année:

1996

Langue:

english

Fichier:

PDF, 172 KB

english, 1996

12

Clinical, electrophysiological and histological analysis in 4 patients with hereditary sensory neuropathy and pyramidal syndrome

M. Zouari, I. Turki, S. Belal, Ch. Ben Hamida, M. Ben Hamida, F. Hentati

Journal:

Neuromuscular Disorders

Année:

1997

Langue:

english

Fichier:

PDF, 266 KB

english, 1997

13

Hereditary sensory neuropathy associated with muscular atrophy affecting 7 members of one kindred

M. Zouari, Ch. Ben Hamida, S. Belal, I. Turki, M. Ben Hamida, F. Hentati

Journal:

Neuromuscular Disorders

Année:

1997

Langue:

english

Fichier:

PDF, 134 KB

english, 1997

14

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

Année:

1997

Langue:

english

Fichier:

PDF, 134 KB

english, 1997

15

Giant axonal neuropathy: clinical study and genetic mapping

C. Ben Hamida, L. Cavalier, S. Belal, H. Sanhaji, N. Nadal, C. Barhoumi, N. Mrissa, N. Maarzouki, J.-L. Mandel, M. Ben Hamida, M. Koenig, F. Hentati

Journal:

Neuromuscular Disorders

Année:

1997

Langue:

english

Fichier:

PDF, 133 KB

english, 1997

16

Ataxia with vitamin E deficiency and Friedreich ataxia: comparative analysis of vitamin A, vitamin E and some lipid parameters in patients and not-affected family members

M. Feki, S. Belal, D. Khiari, M. Zouari, N. Kaabachi, C. Ben Hamida, M. Ben Hamida, A. Mebazaa, F. Hentati

Journal:

Neuromuscular Disorders

Année:

1997

Langue:

english

Fichier:

PDF, 262 KB

english, 1997

17

Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency

M Zouari, M Feki, C Ben Hamida, A Larnaout, I Turki, S Belal, A Mebazaa, M.Ben Hamida, F Hentati

Journal:

Neuromuscular Disorders

Année:

1998

Langue:

english

Fichier:

PDF, 1.08 MB

english, 1998

18

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

Année:

2003

Langue:

english

Fichier:

PDF, 99 KB

english, 2003

19

1-49-03 Hereditary and genetic neurological disorders opportunities for prevention

M. Ben Hamida, M. Zouari, N. Khouja, C. Ben Hamida, A. Larnaout, S. Belal, F. Hentati

Journal:

Journal of the Neurological Sciences

Année:

1997

Langue:

english

Fichier:

PDF, 124 KB

english, 1997

20

Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping

Nicole, Sophie, Hamida, Christiane Ben, Beighton, Peter, Bakouri, Selim, Belal, Samir, Romero, Norma, Viljoen, Denis, Ponsot, Gérard, Sammoud, Azza, Weissenbach, Jean, Fardeau, Michel, Hamida, Mongi B

Journal:

Human Molecular Genetics

Année:

1995

Langue:

english

Fichier:

PDF, 366 KB

english, 1995

21

Clinical and genetic study of familial Parkinson's disease in Tunisia

Gouider-Khouja, N., Belal, S., Hamida, M. B., Hentati, F.

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 155 KB

english, 2000

22

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

Bejaoui, K., Hirabayashi, K., Hentati, F., Haines, J. L., Hamida, C. B., Belal, S., Miller, R. G., McKenna-Yasek, D., Weissenbach, J., Rowland, L. P., Griggs, R. C., Munsat, T. L., Hamida, M. B., Arah

Journal:

Année:

1995

Langue:

english

Fichier:

PDF, 596 KB

english, 1995

23

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family

Mrissa, N., Belal, S., Hamida, C. B., Amouri, R., Turki, I., Mrissa, R., Hamida, M. B., Hentati, F.

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 652 KB

english, 2000

24

Passively Q-switched Erbium-Doped Fiber Laser based on Graphene Oxide as Saturable Absorber

Mansoor, A. K. W., Ahmed Hamida, Belal, Eltaif, Tawfig, Ismail, E. I., Kadir, N. A. A., Khan, Sheroz, Harun, S. W.

Journal:

Journal of Optical Communications

Année:

2017

Langue:

english

Fichier:

PDF, 2.23 MB

english, 2017

25

Relative Humidity Sensing Using A PMMA Doped Agarose Gel Microfiber

Irawati, Ninik, Rahman, Husna A., Yasin, Moh, Al-Askari, Shadi, Hamida, Belal A., Ahmad, Harith, Harun, Sulaiman Wadi

Journal:

Journal of Lightwave Technology

Année:

2017

Langue:

english

Fichier:

PDF, 863 KB

english, 2017

26

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families

Hamida, M. B., Belal, S., Sirugo, G., Hamida, C. B., Panayides, K., Ionannou, P., Beckmann, J., Mandel, J. L., Hentati, F., Koenig, M., Middleton, L.

Journal:

Année:

1993

Langue:

english

Fichier:

PDF, 617 KB

english, 1993

27

[IEEE 2017 IEEE 4th International Conference on Smart Instrumentation, Measurement and Application (ICSIMA) - Putrajaya (2017.11.28-2017.11.30)] 2017 IEEE 4th International Conference on Smart Instrumentation, Measurement and Application (ICSIMA) - Black phosphorus saturable absorber for Q-switched technique pulse generation

Hussein, L A, Hamida, Belal Ahmed, Eltaif, T, Khan, Sheroz, Habaebi, Mohamed Hadi, Zainuddin, Ahmad Anwar, Harun, Sulaiman Wadi

Année:

2017

Fichier:

PDF, 249 KB

2017

28

[IEEE 2019 IEEE 14th Malaysia International Conference on Communication (MICC) - Selangor, Malaysia (2019.12.2-2019.12.4)] 2019 IEEE 14th Malaysia International Conference on Communication (MICC) - Investigation of Q-switched and Mode-Locked Erbium-Doped Fiber Laser Using Graphene oxide-Saturable Absorber

Allah, Belal Ahmed Hamida G., Eltaif, Tawfig A, Omer, Mahamat, Khan, Sheroz

Année:

2019

Fichier:

PDF, 1.60 MB

2019

29

Serum Vitamin E and Lipid-adjusted Vitamin E Assessment in Friedreich Ataxia Phenotype Patients and Unaffected Family Members

Feki, Moncef, Belal, Samir, Feki, Habib, Souissi, Malek, Frih-Ayed, Mahbouba, Kaabachi, Naziha, Hentati, FaycÌ§al, Ben Hamida, Mongi, Mebazaa, Abderraouf

Journal:

Clinical Chemistry

Année:

2002

Fichier:

PDF, 128 KB

2002