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Results of search for 'au:"Ben Hamida, M"', page 3 of 6
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Authors
Amouri, R
Attia, N
Attia-Romdhane, N
Ayed, K
Bejaoui, K
Belal, S
Ben Hamida, C
Ben Hamida, M
Ben Othmane, K
Butler-Browne, G S
Gharbi, N
Hentati, A
Hentati, F
Lapresle, J
Larnaout, A
Letaief, F
Miladi, N
Mrabet, A
Pericak-Vance, M A
Samoud, S
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Chromosome Mapping
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Genes, Recessive
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41.
[2 cases of vascular syndrome of the cranial nerves of ischemic origin].
[electronic resource]
by
Mrabet, A
Jellouli, M
Touibi, S
Ben Hamida, M
Producer:
19890718
In:
Annales de medecine interne
vol. 140
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42.
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.
[electronic resource]
by
Ben Hamida, M
Letaief, F
Hentati, F
Ben Hamida, C
Producer:
19880304
In:
Acta neuropathologica
vol. 75
Online resources:
Available from publisher's website
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43.
[Hemifacial spasm and its treatment with botulinum toxin].
[electronic resource]
by
Gouider-Khouja, N
Turki, I
Ben Hamida, M
Hentati, F
Producer:
19990611
In:
La Tunisie medicale
vol. 77
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44.
[Septicemia in patients undergoing chronic hemodialysis].
[electronic resource]
by
Ben Hamida, M
Hachicha, J
Chaabouni, M N
Jarraya, A
Producer:
19890728
In:
Annales de medecine interne
vol. 140
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45.
[Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases].
[electronic resource]
by
Ben Hamida, M
Letaief, F
Ben Hamida, C
Samoud, S
Producer:
19811014
In:
Journal of the neurological sciences
vol. 50
Online resources:
Available from publisher's website
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46.
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis.
[electronic resource]
by
Ben Hamida, M
Letaief, F
Hentati, F
Ben Hamida, C
Producer:
19870716
In:
Journal of the neurological sciences
vol. 78
Online resources:
Available from publisher's website
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47.
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
[electronic resource]
by
Belal, S
Hentati, F
Ben Hamida, C
Ben Hamida, M
Producer:
19950824
In:
Clinical neuroscience (New York, N.Y.)
vol. 3
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48.
Early onset ataxias in Tunisia. Intrafamilial heterogeneity.
[electronic resource]
by
Ben Hamida, M
Attia-Romdhane, N
Hentati, F
Triki, C
Producer:
19930218
In:
Advances in neurology
vol. 61
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49.
[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty].
[electronic resource]
by
Ben Hamida, M
Ben Othmane, K
Belal, S
Hentati, F
Producer:
19951129
In:
Revue neurologique
vol. 151
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50.
[Treatment of cervical dystonia with botulinum toxin].
[electronic resource]
by
Gouider-Khouja, N
Turki, I
Ben Hamida, M
Hentati, F
Producer:
19990616
In:
La Tunisie medicale
vol. 77
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51.
Phenylketonuria: an underlying etiology of autistic syndrome. A case report.
[electronic resource]
by
Miladi, N
Larnaout, A
Kaabachi, N
Helayem, M
Ben Hamida, M
Producer:
19920429
In:
Journal of child neurology
vol. 7
Online resources:
Available from publisher's website
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52.
[Peripheral neuropathy in a sporadic case of cerebrotendinous xanthomatosis].
[electronic resource]
by
Ben Hamida, M
Chabbi, N
Ben Hamida, C
Mhiri, C
Kallel, R
Producer:
19910821
In:
Revue neurologique
vol. 147
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53.
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings.
[electronic resource]
by
Larnaout, A
Belal, S
Ben Hamida, C
Ben Hamida, M
Hentati, F
Producer:
19980709
In:
Journal of neurology
vol. 245
Online resources:
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54.
[Transformed gastric ulcer (TU) (ulcero-cancer, degenerated ulcer). Apropos of 51 cases].
[electronic resource]
by
Mouchet, A
Marquand, J
Guivarch, M
Godquin, B
Ben Hamida, M F
Producer:
19730717
In:
Journal de chirurgie
vol. 104
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55.
[Congenital fibrolipoma of the mesencephalic protuberation area].
[electronic resource]
by
Larnaout, A
Hentati, F
Ben Hamida, C
Khrouf, N
Ben Hamida, M
Producer:
19950309
In:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
vol. 1
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56.
Limb-girdle muscular dystrophy 2C: clinical aspects.
[electronic resource]
by
Ben Hamida, M
Ben Hamida, C
Zouari, M
Belal, S
Hentati, F
Producer:
19970508
In:
Neuromuscular disorders : NMD
vol. 6
Online resources:
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57.
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
[electronic resource]
by
Ben Hamida, M
Attia-Romdhane, N
Triki, C H
Oueslati, S
Hentati, F
Producer:
19920310
In:
Revue neurologique
vol. 147
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58.
[Brain-type creatine kinase isoenzymes (CK BB) in cerebrovascular accidents].
[electronic resource]
by
Mrabet, A
Gharbi, N
Attia-Romdhane, N
Le Noan, H
Ben Hamida, M
Producer:
19891109
In:
La Tunisie medicale
vol. 67
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59.
[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].
[electronic resource]
by
Ben Hamida, M
Hentati, F
Chebbi, N
Mhiri, C
Ayed, K
Hamzaoui, K
Producer:
19890413
In:
Revue neurologique
vol. 144
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60.
[Acquired factor X deficiency associated with A.L.type amyloidosis. A case report].
[electronic resource]
by
Jeribi, M
Hachicha, J
Ben Hamida, M
Gouiaa, R
Jlidi, R
Jarraya, A
Producer:
19980422
In:
La Tunisie medicale
vol. 74
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