Search Results - "Atmani, Samir"

Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype by EL Bouchikhi, Ihssane, Belhassan, Khadija, Moufid, Fatima Zohra, Bouguenouch, Laila, Samri, Imane, Iraqui Houssaïni, Mohammed, Ouldim, Karim

“…Background Tetralogy of Fallot is the most prevalent cyanotic congenital heart disease, occurring in 1/3 600 live births. This disorder comprises ventricular…”
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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 by El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Belhassan, Khadija, Samri, Imane, Chaouti, Amal, Houssaïni, Mohammed Iraqui, Atmani, Samir, Ouldim, Karim

“…Atrial septal defect (ASD) is one of the most common types of congenital heart disease (CHD). It is mainly caused by mutations of NK2 homeobox 5, GATA binding…”
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Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age by El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Samri, Imane, Abdouss, Fatima, Melhouf, Moulay Abdelilah, Iraqui Houssaini, Mohammed

“…Background Noonan syndrome (NS) is one of the most common RASopathies, with an autosomal dominant inheritance. This disorder is caused by a range of genes…”
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Pediatric recurrent respiratory tract infections: when and how to explore the immune system? (About 53 cases) by El-Azami-El-Idrissi, Mohammed, Lakhdar-Idrissi, Mounia, Chaouki, Sanae, Atmani, Samir, Bouharrou, Abdelhak, Hida, Moustapha

“…Recurrent respiratory tract infections are one of the most frequent reasons for pediatric visits and hospitalization. Causes of this pathology are multiple…”
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Drug Reaction with Eosinophilia and Systemic Symptom (DRESS) induced by carbamazepine: a case report and literature review by E L omairi, Nissrine, Abourazzak, Sanae, Chaouki, Sanae, Atmani, Samir, Hida, Moustapha

“…Drug-induced hypersensitivity or Drug Reaction with Eosinophilia and Systemic Symptom (DRESS) is a severe adverse drug-induced reaction. Diagnosing DRESS is…”
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Multicentric Castleman’s Disease in a Child Revealed by Chronic Diarrhea by Hida, Moustapha, Atmani, Samir, Chaouki, Sana, Benmiloud, Sarra

“…Multicentric Castleman’s disease is a rare benign and unexplained lymphoproliferative disorder that is extremely uncommon in children. It presents with fever,…”
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Cutis Laxa syndrome: a case report by Hbibi, Mohamed, Abourazzak, Sana, Idrissi, Mounia, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

“…Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement…”
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Farber Disease in a Newborn by Sana, Chaouki, Larbi, Elarqam, Samir, Atmani, Abdelhak, Bouharrou, Mustapha, Hida

“…:  Farber disease is a rare lysosomal storage disease characterized by a clinical triad including painful joint deformity, subcutaneous nodules and hoarseness,…”
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P053 The place of ASLOs in the diagnosis of RAA in Morocco by Sara, Himri, Bouchra, Oumokhtar, Samira, El Fakir, Samir, Atmani

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P054 Acute articular rheumatism at the Hassan II hospital center, Fez, Morocco (prospective study: about 152 cases) by Sara, Himri, Bouchra, Oumokhtar, Samira, El Fakir, Samir, Atmani

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P055 Title: Standard rate of ASLO in healthy children with streptococcal (angina) or post-streptococcal (RAA) infection in Morocco by Sara, Himri, Bouchra, Oumokhtar, Fakir Samira, El, Samir, Atmani

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

“…Neonatal coarctation has to be diagnosed and treated urgently. Actually, the surgical treatment is the main option. The coarctation dilatation is usually…”
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Le lupus systémique juvénile familial: à propos de deux familles by Krich, Sanaa, Inani, Kawtar, Meziane, Mariame, Souilmi, Fatima Zohta, Atmani, Samir, Hida, Mustapha, Harmouch, Taoufik, Amarti, Afaf, Mernissi, Fatima Zohra

“…Le lupus érythémateux systémique (LES) juvénile est une connectivite rare, d’évolution plus sévère que chez l'adulte. Les cas familiaux sont exceptionnels. Il…”
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Twelve-years old girl with retro-rectal mass by Arroud, Mounir, Lamiae, Chater, Atmani, Samir, Boujraf, Said, Afifi, My Abderrahmane, Hida, Moustapha, Bouabdallah, Youssef

“…A 12-years-old girl followed for recurrent urinary infections was admitted to the pediatric department complaining of a 1-year history of constipation and…”
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Developmentally supportive care in neonatology: Correlational study of the knowledge and declared practices of professionals by Faez, Naima, Hmami, Fouzia, Kojmane, Widade, Atmani, Samir

“…In the Neonatal Intensive Care Unit, preterm neonates present a neurodevelopmental risk expressed by physiological and behavioral signs that are difficult to…”
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Practices for respecting the newborn's sleep-wake cycle: Interventional study in the neonatal intensive care unit by Faez, Naima, Hmami, Fouzia, Boujraf, Saïd, Kojmane, Widade, Atmani, Samir

“…Premature newborns are exposed to a great deal of over-stimulation, which can affect their cerebral development. For better sleep, certain practices should be…”
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La maladie de Wilson chez l'enfant: à propos de 20 cas by Idrissi, Mounia Lakhdar, Babakhoya, Abdeladim, Khabbache, Kawtar, Souilmi, Fatimzohra, Benmiloud, Sara, Abourrazak, Sanae, Chaouki, Sanae, Atmani, Samir, Bouharrou, Abdelhak, Hida, Moustapha

“…La maladie de Wilson ou dégénérescence hépato-lenticulaire est une affection génétique autosomique récessive caractérisée par une accumulation toxique de…”
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A very old Blalock-Taussig shunt: a case report by Bendoudouch, Houssam, El Boussaadani, Badre, Raissuni, Zainab, Atmani, Samir

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Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations by Ouldim, Karim, Bouguenouch, Laila, Samri, Imane, El Otmani, Ihsan, Hamdaoui, Hasna, Bennis, Sanae, Lakhdar, Mounia Idrissi, Chaouki, Sana, Atmani, Samir, Hida, Moustapha

“…Les syndromes microdélétionnels sont définis par la présence d’une anomalie chromosomique de taille mineure (inférieure à 5 mégabases) ou aneusomie…”
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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot by Škorić-Milosavljević, Doris, Lahrouchi, Najim, Bosada, Fernanda M., Dombrowsky, Gregor, Williams, Simon G., Lesurf, Robert, Tjong, Fleur V.Y., Walsh, Roddy, El Bouchikhi, Ihssane, Breckpot, Jeroen, Audain, Enrique, Ilgun, Aho, Beekman, Leander, Ratbi, Ilham, Strong, Alanna, Muenke, Maximilian, Heide, Solveig, Muir, Alison M., Hababa, Mariam, Cross, Laura, Zhou, Dihong, Pastinen, Tomi, Hitz, Marc-Phillip, Abdul-Khaliq, Hashim, Berger, Felix, Dähnert, Ingo, Dittrich, Sven, Uebing, Anselm, Stiller, Brigitte, Zackai, Elaine, Atmani, Samir, Ouldim, Karim, Adadi, Najlae, Steindl, Katharina, Rauch, Anita, Brook, David, Wilsdon, Anna, Kuipers, Irene, Blom, Nico A., Mulder, Barbara J., Mefford, Heather C., Keren, Boris, Joset, Pascal, Kruszka, Paul, Thiffault, Isabelle, Sheppard, Sarah E., Roberts, Amy, Lodder, Elisabeth M., Keavney, Bernard D., Clur, Sally-Ann B., Mital, Seema, Hitz, Marc-Philip, Christoffels, Vincent M., Postma, Alex V., Bezzina, Connie R.

“…Rare genetic variants in KDR, encoding the vascular endothelial growth factor receptor 2 (VEGFR2), have been reported in patients with tetralogy of Fallot…”
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