Zobrazeno 1 - 10 of 33 pro vyhledávání: '"Emna Turki"'
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Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Autor: Imen Bouchhima, Mariem Damak, Nouha Bouzidi, Chokri Mhiri, Saeed Bohlega, Olfa Hdiji, Emna Turki
Publikováno v: Journal of Movement Disorders. 9:120-123
Woodhouse-Sakati syndrome (WSS) is an infrequent autosomal recessive condition characterized by progressive extrapyramidal signs, mental retardation, hypogonadism, alopecia, and diabetes mellitus. This syndrome belongs to a heterogeneous group of inh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1e028d5890409c0830190aaf9904bf85
https://doi.org/10.14802/jmd.16003
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5
Etat de l’art du problème de localisation ¬routage avec gestion de stock
Autor: Emna Turki, Sonda Elloumi, Diala Dhouib, Abderrahman El mhamedi
Publikováno v: Congrès International de Génie Industriel
Congrès International de Génie Industriel, May 2017, compiègne, France
HAL
International audience
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::508d1c22f30a5311181db09a056daa68
https://hal.archives-ouvertes.fr/hal-01687577
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6
Anxiété et dépression dans la sclérose en plaques : à propos de 100 patients tunisiens
Autor: Sihem Ben Nsir, Mohamed Imed Miladi, Emna Turki, Imen Bouchhima, Mariem Damak, Chokri Mhiri
Publikováno v: L'information psychiatrique. 90:381-386
Objectifs Evaluer les frequences de l’anxiete et de la depression et leur correlation avec le profil clinique chez 100 patients atteints de sclerose en plaques (SEP).Patient et methode Nous avons realise une etude transversale portant sur 100 patie
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c46e48dd0c0dda9e104436ff44abbde
https://doi.org/10.1684/ipe.2014.1207
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7
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Autor: Olfa, Hdiji, Emna, Turki, Nouha, Bouzidi, Imen, Bouchhima, Mariem, Damak, Saeed, Bohlega, Chokri, Mhiri
Publikováno v: Journal of Movement Disorders
Woodhouse-Sakati syndrome (WSS) is an infrequent autosomal recessive condition characterized by progressive extrapyramidal signs, mental retardation, hypogonadism, alopecia, and diabetes mellitus. This syndrome belongs to a heterogeneous group of inh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae9b6c54dc34f1543056a9fba8471dac
https://pubmed.ncbi.nlm.nih.gov/27240811
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8
A fuzzy-based ontology for Alzheimer's disease decision support
Autor: Rafik Bouaziz, Emna Turki, Firas Zekri
Publikováno v: FUZZ-IEEE
The fight against Alzheimer's disease (AD) has become a major issue. We aim to contribute to this fight by seeking to provide adequate software to assist decision makers in the field of AD to choose the optimal decision for each situation. Moreover,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0e59536090c33e1a0b7c4d6de67cda3c
https://doi.org/10.1109/fuzz-ieee.2015.7337922
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9
Confusion mentale chez le sujet âgé
Autor: Nouha Bouzidi, I. Bouchhima, Fatma Smaoui, Mariem Dammak, Mariem Turki, Emna Turki, Chokri Mhiri
Publikováno v: Revue Neurologique. 172:A138-A139
Introduction La confusion mentale represente un trouble neuropsychologique aigu, traduisant un dysfonctionnement global du systeme nerveux central. Le sujet âge, en raison de sa fragilite, est particulierement vulnerable a ce trouble. Objectifs Dres
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5e1f5a18b2d650a17788ae12e96b96ee
https://doi.org/10.1016/j.neurol.2016.01.328
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