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F. Hentati

Veröffentlichungen von F. Hentati zu Hentati, F. ->
weitere Veröffentlichungen von F. Hentati:
Hypertrophic neuropathy in spinocerebellar degeneration (1987)
Familial disorder of the central and peripheral nervous systems with particular cytoplasmic lamellated inclusions in peripheral nerves, muscle satellite cells, and blood capillaries (1985)
Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients (1998)
Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients (1998)
Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients (1998)
Abord latéral du foramen magnum (27 octobre 1989) (1990)
Lateral approach to the foramen magnum (October 27, 1989) (1990)
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria (1994)
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria (1994)
An anatomical study of the motor distribution of the mandibular nerve for a masseteric-facial anastomosis to restore facial function (1997)
An anatomical study of the motor distribution of the mandibular nerve for a masseteric-facial anastomosis to restore facial function (1997)
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings (1998)
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene (1999)
Nasu-Hakola disease in two Tunisian siblings: new radiological findings (2000)
Friedreich’s ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient (1997)
Veröffentlichungen zu Hentati, F.
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1
Hamida, M., Letaief, F., ... Hypertrophic neuropathy in spinocerebellar degeneration
in: Acta neuropathologica , ISSN 1432-0533, Vol. 75 (1. 1987), p. 51-61
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1987
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2
Tomé, F. M. S., Brunet, P., ... Familial disorder of the central and peripheral nervous systems with particular cytoplasmic lamellated inclusions in peripheral nerves, muscle satellite cells, and blood...
in: Acta neuropathologica , ISSN 1432-0533, Vol. 68 (3. 1985), p. 209-217
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1985
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3
Larnaout, A.. Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 29, No. 06 (12. 1998), p. 322-323
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1998
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4
Larnaout, A.. Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 29, No. 06 (12. 1998), p. 322-323
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1998
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5
Larnaout, A.., Belal, S.., ... Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 29, No. 06 (1998), p. 322-323
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1998
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6
Cornu, P., Hentati, K., ... Abord latéral du foramen magnum (27 octobre 1989)
in: Surgical and radiologic anatomy , ISSN 1279-8517, Vol. 12 (1. 1990), p. 23-23
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1990
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7
Cornu, P., Hentati, K., ... Lateral approach to the foramen magnum (October 27, 1989)
in: Surgical and radiologic anatomy , ISSN 1279-8517, Vol. 12 (1. 1990), p. 77-78
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1990
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8
Larnaout, A., Hentati, F., ... Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria
in: Acta neuropathologica , ISSN 1432-0533, Vol. 88 (4. 1994), p. 367-370
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1994
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9
Larnaout, A., Hentati, F., ... Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria
in: Acta neuropathologica , ISSN 1432-0533, Vol. 88 (4. 1994), p. 367-370
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1994
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10
Fournier, H. -D., Denis, F., ... An anatomical study of the motor distribution of the mandibular nerve for a masseteric-facial anastomosis to restore facial function
in: Surgical and radiologic anatomy , ISSN 1279-8517, Vol. 19 (4. 1997), p. 241-244
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1997
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11
Fournier, H.-D., Denis, F., ... An anatomical study of the motor distribution of the mandibular nerve for a masseteric-facial anastomosis to restore facial function
in: Surgical and radiologic anatomy , ISSN 1279-8517, Vol. 19 (4. 1997), p. 241-244
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1997
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12
Larnaout, A., Belal, S., ... Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings
in: Journal of neurology , ISSN 1432-1459, Vol. 245 (4. 1998), p. 231-235
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1998
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13
Nicole, S., White, P.S., ... The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene
in: Human genetics , ISSN 1432-1203, Vol. 105 (1/2. 1999), p. 98-103
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1999
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14
Chaabane, M., Larnaout, A., ... Nasu-Hakola disease in two Tunisian siblings: new radiological findings
in: Neuroradiology , ISSN 1432-1920, Vol. 42 (5. 2000), p. 375-378
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2000
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15
Larnaout, A., Belal, S., ... Friedreich’s ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient
in: Acta neuropathologica , ISSN 1432-0533, Vol. 93 (6. 1997), p. 633-637
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1997
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16
Larnaout, A., Mongalgi, M. A., ... Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (6. 1998), p. 639-644
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1998
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17
Kaabachi, N., Larnaout, A., ... Familial encephalopathy andl-2-hydroxyglutaric aciduria
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (5. 1993), p. 893-893
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1993
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18
Ben Hamida, C., Doerflinger, N., ... Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 5, No. 2 (1993), p. 195-200
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1993
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19
Fontaine, B., Nicole, Sophie, ... Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval
in: Human genetics , ISSN 1432-1203, Vol. 98 (3. 1996), p. 380-385
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1996
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20
Hamida, C.B., Cavalier, L., ... Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
in: Neurogenetics , ISSN 1364-6753, Vol. 1 (2. 1997), p. 129-133
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1997