Publications by authors named "Walid Sayed"

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Evaluation of the antibacterial and cytotoxic properties of TotalFill and NeoSEALER flo bioceramic sealers.
Sabatiny Sebastian, Walid El-Sayed, Pooja Adtani, Rania Faouzi Zaarour, Aswathy Nandakumar

J Conserv Dent Endod· May 2024

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Prediction of Lymphovascular and Perineural Invasion of Oral Squamous Cell Carcinoma by Combined Expression of p63 and Cyclin D1.
Natheer H Al-Rawi, Sausan Al Kawas, Muwaffaq Al Ani, Ahmed Sameer Alnuaimi, Walid El-Sayed

Eur J Dent· October 2023

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Measurement of student engagement in health professions education: a review of literature.
Salah Eldin Kassab, Mohamed Al-Eraky, Walid El-Sayed, Hossam Hamdy, Henk Schmidt

BMC Med Educ· May 2023

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Effect of different teaching/learning approaches using virtual patients on student's situational interest and cognitive load: a comparative study.
Sura Ali Fuoad, Walid El-Sayed, Hesham Marei

BMC Med Educ· November 2022

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Student engagement in undergraduate medical education: A scoping review.
Salah Eldin Kassab, Walid El-Sayed, Hossam Hamdy

Med Educ· July 2022

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Gingival Depigmentation Using Diode 980 nm and Erbium-YAG 2940 nm Lasers: A Split-Mouth Clinical Comparative Study.
Zaid Kamel Jnaid Harb, Walid El-Sayed, Jumma Alkhabuli

Int J Dent· December 2021

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Popliteal artery entrapment syndrome secondary to a femoral osteochondroma.
Maamoun Mihoubi, Walid Sayed, Oussama Barkallah, Mondher Mbarek

Tunis Med· December 2020

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Role of Hypoxic Stress in Regulating Tumor Immunogenicity, Resistance and Plasticity.
Stéphane Terry, Rania Faouzi Zaarour, Goutham Hassan Venkatesh, Amirtharaj Francis, Walid El-Sayed

Int J Mol Sci· October 2018

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Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
David A Parry, Claire E L Smith, Walid El-Sayed, James A Poulter, Roger C Shore

Am J Hum Genet· October 2016

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A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency.
David A Parry, Tim D Holmes, Nikita Gamper, Walid El-Sayed, Nishani T Hettiarachchi

J Allergy Clin Immunol· March 2016

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[Hibernoma of the thigh. A case report].
Walid Sayed, Hachem Mahjoub, Houssem Dougaz, Mohamed Ben Salah, Mohsen Trabelsi

Tunis Med· April 2015

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[Paraspinal hydatid cyst: A rare localization of hydatidosis].
Walid Sayed, Mohamed Ben Salah, Mohamed Zoghlami, Amine Bennour, Moez Dridi

Tunis Med· March 2015

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[Desmoid fibromatosis of the lower limb].
Walid Sayed, Mehdi Bellil, Sabri Mahjoub, Taieb Raboudi, Moez Dridi

Tunis Med· March 2015

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Intra-articular tenosynovial giant cell tumor arising from the posterior cruciate ligament.
Walid Sayed, Elifa Daghfous, Mohamed Ben Salah, Sabri Mahjoub, Moez Dridi

Tunis Med· February 2015

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Simultaneous bilateral tibial stress fractures in a handball player.
Walid Sayed, Mohamed Ali Kedous, Mohamed Ben Salah, Mohamed Zoghlami, Moez Dridi

Tunis Med· February 2015

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Epidural hematoma due to spinal epidural anaesthesia.
Walid Sayed, Mongi Miledi, Mohamed Ben Salah, Mohamed Zoghlami, Moez Dridi

Tunis Med· January 2015

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Pseudotumoral chronic osteomyelitis with multifocal involvement.
Walid Sayed, Taieb Raboudi, Mohamed Ben Salah, Wael Chebbi, Moez Dridi

Tunis Med· December 2014

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[Reduction spontanée d'une luxation d'une Prothèse totale de hanche associée a une Dislocation entre la tête et le col prothétique].
Walid Sayed, Mourad Zaraa, Zied Oueslati, Zied Chenguel, Moez Dridi

Tunis Med· November 2014

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Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta.
James A Poulter, Walid El-Sayed, Roger C Shore, Jennifer Kirkham, Chris F Inglehearn

Eur J Hum Genet· January 2014

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Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.
David A Parry, Steven J Brookes, Clare V Logan, James A Poulter, Walid El-Sayed, Jihad Sayed

Am J Hum Genet· September 2012

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Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.
Walid El-Sayed, David A Parry, Roger C Shore, Mushtaq Ahmed, Hussain Jafri

Am J Hum Genet· November 2009

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Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
David A Parry, Alan J Mighell, Walid El-Sayed, Roger C Shore, Ismail K Jalili

Am J Hum Genet· February 2009

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Sternal cleft, a rare congenital anomaly. Report of the first Tunisian case.
Walid Sayed, Youssef Hellal, Nejib Kaabar, Mohamed Ben Hariz, Kamel Ben Fadhel, Sadok Sayed

Tunis Med· December 2008

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