Author

Amel Mrad

Observed institutions: Cleveland Clinic, Inserm, University of Monastir, Hôpital Mongi Slim, Hôpital Lariboisière, Habib hospital Thameur, Hospital Fatuma Bourguiba Monastir, Université Paris Diderot, Cleveland Clinic Research

OpenAlex ID: A5113547031

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

2006 · Dhouha Darghouth, Kevin W. Hallgren, et al. · Blood · 44

Neurological soft signs in euthymic bipolar I patients: A comparative study with healthy siblings and controls

2015 · Amel Mrad, Mohamed Wassim Krir, et al. · Psychiatry Research · 31

Correlations between obstetric complications and neurological soft signs in Tunisian patients with schizophrenia

2010 · Amel Mrad, Anwar Mechri, et al. · Psychiatry and Clinical Neurosciences · 7

Persistent auditory hallucinations in out-patients with schizophrenia.

2016 · Soumaya Chatti, Wassim Ben Mansour, et al. · PubMed · 4

Resolution of Tardive Dyskinesia with Clozapine: A Case Report

2016 · Badii Amamou, Nesrine Essid, et al. · Dual Diagnosis Open Access · 4

Traitement par rispéridone d’une polydipsie avec hyponatrémie sévère chez un patient schizophrène

2014 · Maha Chhoumi, Amel Mrad, et al. · Therapies · 1

Burnout Among Tunisian Geriatric Caregivers

2018 · Amel Mrad

Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family.

2005 · Dhouha Darghouth, Kevin W. Hallgren, et al. · Blood

[Seasonal depressive disorder: a controlled study in Tunisian psychiatric sample].

2004 · Anwar Mechri, Férid Zaafrane, et al. · PubMed

Contribution à l'étude des hémoglobines anormales : épidémiologie, structure, fonction des hémoglobines anormales en Tunisie

1993 · Amel Mrad

Works count: 10

Citation count: 91

H-index: 4

I10-index: 2