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Amale Hassani

Showing results (1-10 of 7) with videos related to

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Sultan Qaboos University Medical Journal|March 11, 2026
Novel <i>ANKRD11</i> Mutation in KBG Syndrome: <i>A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping</i>Azzeddine Laaraje, Khadija Belcadi Abassi, Mouna Lemaamer, et al.
European Journal of Dermatology : EJD|August 12, 2008
Hypersensitivity to cyclooxygenase inhibitory drugs in children: a study of 164 casesAmale Hassani, Claude Ponvert, Chantal Karila, et al.
The Pan African Medical Journal|December 1, 2017
[Double aortic arch: about two cases]Sihame Lemouakni, Amale Hassani, Hakim Elyajouri, et al.
The Pan African Medical Journal|May 19, 2026
[Pulmonary hemosiderosis revealing class II HLA deficiency in a 9-month-old infant: a case report]Lemrabott Hamada Beddi, Amale Hassani, Brahim Elhasbaoui, et al.
Cytogenetic and Genome Research|December 18, 2017
Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural DeafnessSaadia Amasdl, Wiam Smaili, Abdelhafid Natiq, et al.
Oxford Medical Case Reports|April 16, 2026
Type 3 Von Willebrand disease: two clinical cases of a rare disorderKhadija Belcadi Abassi, Karima Larbi Ouassou, Abdelilah Radi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 28, 2024
Cytogenetic abnormalities and TP53 and RAS gene profiles of childhood acute lymphoblastic leukemia in MoroccoHanaa Skhoun, Meriem El Fessikh, Mohamed El Alaoui Al Abdallaoui, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Sultan Qaboos University Medical Journal|March 11, 2026
Novel <i>ANKRD11</i> Mutation in KBG Syndrome: <i>A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping</i>Azzeddine Laaraje, Khadija Belcadi Abassi, Mouna Lemaamer, et al.
European Journal of Dermatology : EJD|August 12, 2008
Hypersensitivity to cyclooxygenase inhibitory drugs in children: a study of 164 casesAmale Hassani, Claude Ponvert, Chantal Karila, et al.
The Pan African Medical Journal|December 1, 2017
[Double aortic arch: about two cases]Sihame Lemouakni, Amale Hassani, Hakim Elyajouri, et al.
The Pan African Medical Journal|May 19, 2026
[Pulmonary hemosiderosis revealing class II HLA deficiency in a 9-month-old infant: a case report]Lemrabott Hamada Beddi, Amale Hassani, Brahim Elhasbaoui, et al.
Cytogenetic and Genome Research|December 18, 2017
Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural DeafnessSaadia Amasdl, Wiam Smaili, Abdelhafid Natiq, et al.
Oxford Medical Case Reports|April 16, 2026
Type 3 Von Willebrand disease: two clinical cases of a rare disorderKhadija Belcadi Abassi, Karima Larbi Ouassou, Abdelilah Radi, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 28, 2024
Cytogenetic abnormalities and TP53 and RAS gene profiles of childhood acute lymphoblastic leukemia in MoroccoHanaa Skhoun, Meriem El Fessikh, Mohamed El Alaoui Al Abdallaoui, et al.
Pageof 1