Publications by authors named "Samir Atmani"

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A very old Blalock-Taussig shunt: a case report.
Houssam Bendoudouch, Badre El Boussaadani, Zainab Raissuni, Samir Atmani

Eur Heart J Case Rep· April 2024

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Practices for respecting the newborn's sleep-wake cycle: Interventional study in the neonatal intensive care unit.
Naima Faez, Fouzia Hmami, Saïd Boujraf, Widade Kojmane, Samir Atmani

J Neurosci Rural Pract· February 2024

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Developmentally supportive care in neonatology: Correlational study of the knowledge and declared practices of professionals.
Naima Faez, Fouzia Hmami, Widade Kojmane, Samir Atmani

Ann Med Surg (Lond)· December 2022

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Percutaneous coarctation dilatation under transthoracic echocardiography guidance solely without fluoroscopy in neonate intensive care.
Samir Atmani, Said Belmkaddem, Moustapha Elkouach

Cardiol Young· November 2021

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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, Gregor Dombrowsky, Simon G Williams, Samir Atmani

Genet Med· October 2021

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Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M Bosada, Gregor Dombrowsky, Simon G Williams, Samir Atmani

Genet Med· October 2021

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Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Khadija Belhassan, Imane Samri, Samir Atmani

Eurasian J Med· October 2020

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Anomalous origin of left pulmonary artery from the ascending aorta: echocardiography assessment.
Samir Atmani, Imane Bendris

Cardiol Young· January 2020

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[Isolated splenomegaly during congenital cytomegalovirus infection].
Widade Kojmane, Fouzia Hmami, Samir Atmani

Presse Med· March 2019

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Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).
Ihssane El-Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Karim Ouldim, Samir Atmani

Turk J Pediatr· January 2019

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GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
Ihssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Laila Bouguenouch, Samir Atmani

Afr Health Sci· December 2018

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Pediatric recurrent respiratory tract infections: when and how to explore the immune system? (About 53 cases).
Mohammed El-Azami-El-Idrissi, Mounia Lakhdar-Idrissi, Sanae Chaouki, Samir Atmani, Abdelhak Bouharrou

Pan Afr Med J· March 2017

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NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.
Ihssane El Bouchikhi, Laila Bouguenouch, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Khadija Belhassan, Samir Atmani

Anatol J Cardiol· March 2017

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Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate.
Ihssane El Bouchikhi, Khadija Belhassan, Fatima Zohra Moufid, Mohammed Iraqui Houssaini, Laila Bouguenouch, Samir Atmani

Int J Pediatr Adolesc Med· December 2016

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[Family Juvenile Systemic Lupus: about two families].
Sanaa Krich, Kawtar Inani, Mariame Meziane, Fatima Zohta Souilmi, Samir Atmani

Pan Afr Med J· April 2016

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What prognosis for Ebstein's anomaly without surgery? Hassan II teaching hospital experience.
Moumouni Garba, Samir Atmani, Rabiou Sani, Kaled Adamou Nouhou

Tunis Med· April 2016

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Cutis Laxa syndrome: a case report.
Mohamed Hbibi, Sana Abourazzak, Mounia Idrissi, Sana Chaouki, Samir Atmani

Pan Afr Med J· March 2016

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[Acute disseminated encephalomyelitis in children].
Ilham Tadmori, Sana Chaouki, Sana Abourazzak, Souilmi Fatima Zahra, Sarra Benmiloud, Samir Atmani

Pan Afr Med J· November 2015

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Drug Reaction with Eosinophilia and Systemic Symptom (DRESS) induced by carbamazepine: a case report and literature review.
Nissrine E L omairi, Sanae Abourazzak, Sanae Chaouki, Samir Atmani, Moustapha Hida

Pan Afr Med J· July 2015

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The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies.
Ihssane El Bouchikhi, Imane Samri, Mohammed Iraqui Houssaini, Saaid Trhanint, Laila Bouguenouch, Samir Atmani

Turk J Med Sci· July 2015

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Multicentric Castleman's Disease in a Child Revealed by Chronic Diarrhea.
Sarra Benmiloud, Sana Chaouki, Samir Atmani, Moustapha Hida

Case Rep Pediatr· March 2015

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[Wilson's disease in the child: apropos of 20 cases].
Mounia Lakhdar Idrissi, Abdeladim Babakhoya, Kawtar Khabbache, Fatimzohra Souilmi, Sara Benmiloud, Samir Atmani

Pan Afr Med J· September 2013

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[Apert syndrome].
Sarra Benmiloud, Sana Chaouki, Samir Atmani, Moustapha Hida

Pan Afr Med J· September 2013

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[Involuntary movements in infantile cobalamin deficiency appearing during treatment].
Sana Abourazzak, Sana Chaouki, Meryem Boubou, Moncef Amrani, Samir Atmani

Presse Med· April 2013

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Gelastic seizures and fever originating from a parietal cortical dysplasia.
Sana Chaouki, Saïd Boujraf, Samir Atmani, Larbi Elarqam, Wafae Messouak

J Pediatr Neurosci· January 2013

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