Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Amel, Mrad"'
Publikováno v:
Psychiatry Research. 236:173-178
Neurological Soft Signs (NSS) are endophenotypic markers widely studied in schizophrenia and remain poorly evaluated in bipolar disorder. The aims of this paper were to determine the prevalence and scores of NSS in bipolar I patients, compared to hea
Autor:
Soumaya, Chatti, Wassim, Ben Mansour, Jérôme, Brunelin, Amel, Mrad, Mohamed, Saoud, Leila, Gassab, Emmanuel, Poulet, Anwar, Mechri
Publikováno v:
La Tunisie medicale. 94(5)
Objectives to estimate the prevalence of persistent auditory hallucinations (AHs) in a group of schizophrenic patients, to evaluate their dimensions and to identify their clinical associated factors. Method This was a cross-sectional study carried-on
Publikováno v:
Dual Diagnosis: Open Access. 1
Tardive dyskinesia is an extrapyramidal side effect that can occur after a prolonged use of antipsychotic medication, it appears to be about 0.4% to 4% worldwide. Prior reports suggest that clozapine may be effective in the management of tardive dysk
Publikováno v:
Psychiatry and Clinical Neurosciences. 64:645-648
The objective of this study was to examine the correlations between a history of obstetric complications (OC) and neurological soft signs (NSS) in Tunisian patients with schizophrenia. Forty-six patients were assessed using the Krebs et al. NSS scale
Publikováno v:
Annales Médico-psychologiques, revue psychiatrique. 166:646-652
Resume Les objectifs de ce travail etaient de comparer la frequence des complications obstetricales chez des patients schizophrenes par rapport a leurs apparentes et a des temoins sains et de rechercher les correlations entre ces complications et les
Publikováno v:
L'Encéphale. 33:762-767
Resume L’objectif de ce travail etait de comparer les caracteristiques sociodemographiques et cliniques des patients bipolaires type I en fonction de la presence ou non d’antecedents familiaux thymiques afin d’identifier certaines caracteristiq
Autor:
Dhouha Darghouth, Kevin W. Hallgren, Sophie Lericousse, Jean Rosa, Kathleen L. Berkner, Youssef Gharbi, Radhia Kastally, Amel Mrad, Rebecca L. Shtofman, Ahmed Maherzi
Publikováno v:
Blood. 108:1925-1931
Hereditary combined vitamin K–dependent (VKD) coagulation factor deficiency is an autosomal recessive bleeding disorder associated with defects in either the γ-carboxylase, which carboxylates VKD proteins to render them active, or the vitamin K ep
Publikováno v:
L'Encéphale. 31:65-71
Resume Les objectifs de ce travail etaient d’estimer la frequence des suicidants a repetition parmi l’ensemble des suicidants admis aux urgences et de comparer les caracteristiques des suicidants a repetition et des primosuicidants afin de degage