Search Results - "Hamdan, Dina"

Cross-sectional imaging of pancreatic leak: a pictorial review by Cardoso, Daniel, Miranda, Joao, de Arimateia Batista Araujo-Filho, Jose, Soares, Luciana Eltz, Chagas, Lucia, Seidel, Kamila, Fonseca, Gilton Marques, Hamdan, Dina, Kalaycioglu, Bora, Chhabra, Shalini, Yildirim, Onur, Chakraborty, Jayasree, Horvat, Natally

“…Pancreatic leaks occur when a disruption in the pancreatic ductal system results in the leakage of pancreatic enzymes such as amylase, lipase, and proteases…”
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CT Imaging Assessment of Pancreatic Adenocarcinoma Resectability after Neoadjuvant Therapy: Current Status and Perspective on the Use of Radiomics by Khasawneh, Hala, Ferreira Dalla Pria, Hanna Rafaela, Miranda, Joao, Nevin, Rachel, Chhabra, Shalini, Hamdan, Dina, Chakraborty, Jayasree, Biachi de Castria, Tiago, Horvat, Natally

“…Pancreatic adenocarcinoma (PDAC) is the most common pancreatic cancer and is associated with poor prognosis, a high mortality rate, and a substantial number of…”
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Hereditary Folate Malabsorption presenting as neutropenic fever in a newborn from the first Palestinian family with the novel SLC46A1-mutation, A-case-report by Sarhan, Fajr M.A., Jobran, Afnan W.M., Mansour, Islam I.A., Dukmak, Osama N., Rashed, Mohammed A.M., Hamdan, Dina M.A., Abdalhadi, Israa A.A.

“…Hereditary Folate Malabsorption (HFM) is an extremely rare autosomal recessive disorder with in the existence of only 30 families world-wide. It presents with…”
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Effects of Smoking on Outcomes of Anti-Vascular Endothelial Growth Factor Therapy in Patients with Diabetic Macular Edema: A Retrospective Case-Control Study by Al Saad, Mouna, Shehadeh, Amin, Hizzani, Asem, Alzibdeh, Abdulla, Alsubhi, Amani A, Hamdan, Dina, Alkubati, Ebtehal, Meqbil, Jehad, Hamadneh, Lina, Ababneh, Osama

“…To determine the effect of smoking on the response to anti-vascular endothelial growth factor (anti-VEGF) therapy treatment in patients with diabetic macular…”
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Hereditary Folate Malabsorption presenting as neutropenic fever in a newborn from the first Palestinian family with the novel SLC46A1-mutation, A-case-report by Sarhan, Fajr M A, Jobran, Afnan W M, Mansour, Islam I A, Dukmak, Osama N, Rashed, Mohammed A M, Hamdan, Dina M A, Abdalhadi, Israa A A

“…Introduction and importanceHereditary Folate Malabsorption (HFM) is an extremely rare autosomal recessive disorder with in the existence of only 30 families…”
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Negative effect of Ni on PtHY in n-pentane isomerization evidenced by IR and ESR studies by Aziz, Muhammad Arif Ab, Kamarudin, Nur Hidayatul Nazirah, Setiabudi, Herma Dina, Hamdan, Halimaton, Jalil, Aishah Abdul, Triwahyono, Sugeng

“…Ni/PtHY with different Ni loadings was prepared by impregnating HY with hexachloroplatinic acid solution and Ni2＋/N,N-dimethylformamide solution. An increase…”
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