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Rim Amrani

Showing results (21-30 of 33) with videos related to

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International Journal of Neonatal Screening|July 23, 2025
Implementation of Neonatal Screening Program for Congenital Hypothyroidism in Eastern MoroccoFatima Wahoud, Samia Essadki, Khadija Zirar, et al.
Cureus|August 18, 2025
Spontaneous Neonatal Gastric Perforation: A Case ReportAbir Azirar, Mohammed Ech-Chebab, Anass Ayyad, et al.
Cureus|May 6, 2026
Neonatal Spina Bifida: Clinical Profile, Management, and Maternal Characteristics in a Moroccan Tertiary CenterMohammed Ech-Chebab, Inasse Lamouri, Anass Ayyad, et al.
Cureus|March 14, 2025
Cerebral Sinovenous Thrombosis in Neonates: A Report of Three CasesOlfa Asbik, Sahar Messaoudi, Mohammed Ech-Chebab, et al.
Cureus|December 4, 2025
Giant Prenatally Diagnosed Cervicofacial Cystic Lymphangioma in a Term Neonate: Case Report and Literature ReviewWijdane Lemcirdi, Hanae Bahari, Mohammed Ech-Chebab, et al.
Cureus|August 9, 2024
Hypokinetic Hypertrophic Cardiomyopathy: A Rare Case of a Spontaneously Regressive Form in a NewbornInasse Lamouri, Mohammed Ech-Chebab, Anass Ayyad, et al.
Annales De Biologie Clinique|July 21, 2023
[Contribution of cytogenetic in the diagnosis of Edwards's syndrome: about 9 cases]Fatima Ezzahra Aouni, Khawla Zerrouki, Fatimazahra Smaili, et al.
Annals of Medicine and Surgery (2012)|October 25, 2021
<i>Leclercia adecarboxylata</i> invasive infection in a patient with Hirschsprung disease: A case reportAdnane Aarab, Abderrazak Saddari, Benhamza Noussaiba, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 10, 2026
Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan PatientsImane Cherkaoui, Saida Lhousni, Manal Elidrissi Errahhali, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 23, 2024
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism arrayManal Elidrissi Errahhali, Mounia Elidrissi Errahhali, Sara Ramdani, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
International Journal of Neonatal Screening|July 23, 2025
Implementation of Neonatal Screening Program for Congenital Hypothyroidism in Eastern MoroccoFatima Wahoud, Samia Essadki, Khadija Zirar, et al.
Cureus|August 18, 2025
Spontaneous Neonatal Gastric Perforation: A Case ReportAbir Azirar, Mohammed Ech-Chebab, Anass Ayyad, et al.
Cureus|May 6, 2026
Neonatal Spina Bifida: Clinical Profile, Management, and Maternal Characteristics in a Moroccan Tertiary CenterMohammed Ech-Chebab, Inasse Lamouri, Anass Ayyad, et al.
Cureus|March 14, 2025
Cerebral Sinovenous Thrombosis in Neonates: A Report of Three CasesOlfa Asbik, Sahar Messaoudi, Mohammed Ech-Chebab, et al.
Cureus|December 4, 2025
Giant Prenatally Diagnosed Cervicofacial Cystic Lymphangioma in a Term Neonate: Case Report and Literature ReviewWijdane Lemcirdi, Hanae Bahari, Mohammed Ech-Chebab, et al.
Cureus|August 9, 2024
Hypokinetic Hypertrophic Cardiomyopathy: A Rare Case of a Spontaneously Regressive Form in a NewbornInasse Lamouri, Mohammed Ech-Chebab, Anass Ayyad, et al.
Annales De Biologie Clinique|July 21, 2023
[Contribution of cytogenetic in the diagnosis of Edwards's syndrome: about 9 cases]Fatima Ezzahra Aouni, Khawla Zerrouki, Fatimazahra Smaili, et al.
Annals of Medicine and Surgery (2012)|October 25, 2021
<i>Leclercia adecarboxylata</i> invasive infection in a patient with Hirschsprung disease: A case reportAdnane Aarab, Abderrazak Saddari, Benhamza Noussaiba, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 10, 2026
Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan PatientsImane Cherkaoui, Saida Lhousni, Manal Elidrissi Errahhali, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 23, 2024
First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism arrayManal Elidrissi Errahhali, Mounia Elidrissi Errahhali, Sara Ramdani, et al.
Pageof 4