Search Results - "Almousa, Maher"

Documentation of a novel FBP1 gene mutation in the Arabian ethnicity: a case report by Almousa, Maher, Aljomaa, Mohammad, Hamey, Shekhey, Alasmar, Diana

“…Fructose-1,6-bisphosphatase deficiency is a rare autosomal recessive disorder characterized by impaired gluconeogenesis. Fructose-1,6-bisphosphatase 1 (FBP1)…”
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Hydropneumothorax caused by complete rupture of a pulmonary hydatid cyst: A rare case report by Almousa, Maher, Alhadla, Ahmad, Aljomaa, Mohammad, Abdalrazzak, Tamim

“…Key Clinical Message Hydatid disease is a zoonotic disease endemic in developing regions. It is usually caused by infection with the tapeworm Echinococcus…”
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Neurofibromatosis type 1 in Syrian older patient presented with gastric outlet obstruction by Almousa, Maher, Albeiruti, Ahmad, Aljomaa, Mohammad, Aleter, Assem, Jarad, Youssef

“…Neurofibromatosis type 1 is an autosomal dominant disorder with cutaneous features and multiple tumors that involve different organs. Gastrointestinal stromal…”
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Cholera outbreak and debilitated health facilities in Syria: urgent need for support and action by Almousa, Maher, Aljomaa, Mohammad

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Successful surgical reconstruction of atypical variant mirror hand anomaly in a 2-year-old female child: a unique case report by Arab, Hazem, Almousa, Maher, Salemah, Mahmoud, Alsaffaf, Yousef, Alabdullah, Abdulla

“…Mirror hand is an extremely rare congenital abnormality characterized by polydactyly and duplication of the ulna, with the absence of the radius and thumb…”
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Spider angioma at the injection site of the meningitis vaccine by Alabdullah, Hadi, Almousa, Maher, Alabdullah, Muhammad Nour, Al-shawaf, Ahmad Zahi, Douri, Thaer

“…Abstract Spider angioma is a cutaneous nevus caused by a vascular abnormality, characterized by a central red area with radiating reddish, web-like extensions…”
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Dynamics of disease characteristics and clinical management of critically ill COVID-19 patients over the time course of the pandemic: an analysis of the prospective, international, multicentre RISC-19-ICU registry by Wendel-Garcia, Pedro David, Moser, André, Jeitziner, Marie-Madlen, Aguirre-Bermeo, Hernán, Arias-Sanchez, Pedro, Apolo, Janina, Roche-Campo, Ferran, Franch-Llasat, Diego, Kleger, Gian-Reto, Schrag, Claudia, Pietsch, Urs, Filipovic, Miodrag, David, Sascha, Stahl, Klaus, Bouaoud, Souad, Ouyahia, Amel, Fodor, Patricia, Locher, Pascal, Siegemund, Martin, Zellweger, Nuria, Cereghetti, Sara, Schott, Peter, Gangitano, Gianfilippo, Wu, Maddalena Alessandra, Alfaro-Farias, Mario, Vizmanos-Lamotte, Gerardo, Ksouri, Hatem, Gehring, Nadine, Rezoagli, Emanuele, Turrini, Fabrizio, Lozano-Gómez, Herminia, Carsetti, Andrea, Rodríguez-García, Raquel, Yuen, Bernd, Weber, Anja Baltussen, Castro, Pedro, Escos-Orta, Jesus Oscar, Dullenkopf, Alexander, Martín-Delgado, Maria C., Aslanidis, Theodoros, Perez, Marie-Helene, Hillgaertner, Frank, Ceruti, Samuele, Franchitti Laurent, Marilene, Marrel, Julien, Colombo, Riccardo, Laube, Marcus, Fogagnolo, Alberto, Studhalter, Michael, Wengenmayer, Tobias, Gamberini, Emiliano, Buerkle, Christian, Buehler, Philipp K., Keiser, Stefanie, Elhadi, Muhammed, Montomoli, Jonathan, Guerci, Philippe, Fumeaux, Thierry, Schuepbach, Reto A., Jakob, Stephan M., Que, Yok-Ai, Hilty, Matthias Peter, Hilty, Matthias P., Wendel-Garcia, Pedro, Abdoun, Meriem, Rais, Mounira, Caballero, Angel, Tschoellitsch, Thomas, Meier, Jens, Martinez, Luis A., Tirapé-Castro, Hugo, Galal, Islam, Tharwat, Samar, Abdehaleem, Ibrahim, Jurkolow, Geoffrey, Novy, Emmanuel, Losser, Marie-Reine, Zotzmann, Viviane, Seeliger, Benjamin, Welte, Tobias, Korsos, Anita, Ahmed, Luqman Abdulkhudhur, Hashim, Hashim Talib, Nikandish, Reza, Casarotta, Erika, Giaccaglia, Paolo, Giacomini, Matteo, Magliocca, Aurora, Bolondi, Giuliano, Potalivo, Antonella, Salvi, Luca, Wu, Maddalena A., Cogliati, Chiara, Catena, Emanuele, Simonini, Maria S., Fabbri, Silvia, Bitondo, Maria M., Maciopinto, Francesca, de Camillis, Enrico, Venturi, Marta

“…Abstract Background It remains elusive how the characteristics, the course of disease, the clinical management and the outcomes of critically ill COVID-19…”
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Successful surgical reconstruction of atypical variant mirror hand anomaly in a 2-year-old female child: a unique case report by Arab, Hazem, Almousa, Maher, Salemah, Mahmoud, Alsaffaf, Yousef, Alabdullah, Abdulla

“…IntroductionMirror hand is an extremely rare congenital abnormality characterized by polydactyly and duplication of the ulna, with the absence of the radius…”
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Spider angioma at the injection site of the meningitis vaccine by Alabdullah, Hadi, Almousa, Maher, Alabdullah, Muhammad Nour, Al-Shawaf, Ahmad Zahi, Douri, Thaer

“…Spider angioma is a cutaneous nevus caused by a vascular abnormality, characterized by a central red area with radiating reddish, web-like extensions. It is…”
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Neurofibromatosis type 1 in Syrian older patient presented with gastric outlet obstruction by Almousa, Maher, Albeiruti, Ahmad, Aljomaa, Mohammad, Aleter, Assem, Jarad, Youssef

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