Anmelden/Registrieren
Erscheinungsjahr:
 
Zurück zur geteilten Ansicht
F. Hentati

Veröffentlichungen von F. Hentati zu Hamida, C. ->
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 Hamida, C.
Zurück zur geteilten Ansicht
Verfasser Titel Jahr absteigend sortierenaufsteigend sortieren
zeige Details
1
Hamida, M., Letaief, F., ... Hypertrophic neuropathy in spinocerebellar degeneration
in: Acta neuropathologica , ISSN 1432-0533, Vol. 75 (1. 1987), p. 51-61
Zugang: zum Volltext
ähnliche Vorschläge
1987
zeige Details
2
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
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
3
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
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
4
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
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
5
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
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
6
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
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
7
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
Zugang: zum Volltext
ähnliche Vorschläge
1997
zeige Details
8
Ben Othmane, Kamel, Ben Hamida, Mongi, ... Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 2, No. 4 (1992), p. 315-317
Zugang: zum Volltext
ähnliche Vorschläge
1992
zeige Details
9
Hentati, Afif, Bejaoui, Khemissa, ... Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 7, No. 3 (1994), p. 425-428
Zugang: zum Volltext
ähnliche Vorschläge
1994
zeige Details
10
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
Zugang: zum Volltext
ähnliche Vorschläge
1996
zeige Details
11
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
Zugang: zum Volltext
ähnliche Vorschläge
1993
zeige Details
12
Idzko, Marco, Hammad, Hamida, ... Extracellular ATP triggers and maintains asthmatic airway inflammation by activating dendritic cells
in: Nature medicine . - New York, NY : Nature America Inc., ISSN 1546-170X, Vol. 13, No. 8 (2007), p. 913-919
Zugang: zum Volltext
ähnliche Vorschläge
2007
zeige Details
13
Hosler, Betsy A., Sapp, Peter C., ... Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33
in: Neurogenetics , ISSN 1364-6753, Vol. 2 (1. 1998), p. 34-42
Zugang: zum Volltext
ähnliche Vorschläge
1998
zeige Details
14
Yang, Yi, Hentati, Afif, ... The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 29, No. 2 (2001), p. 160-165
Zugang: zum Volltext
ähnliche Vorschläge
2001
zeige Details
15
Harms, L., Bock, A., ... Fourth metting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (1. 1994), p. 1-164
Zugang: zum Volltext
ähnliche Vorschläge
1994