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Journal of Bone and Mineral Metabolism|August 6, 2009
An autosomal dominant hypophosphatemic rickets phenotype in a Tunisian family caused by a new FGF23 missense mutationMoez Gribaa, Mohamed Younes, Yosra Bouyacoub, et al.Iranian Journal of Pathology|July 11, 2026
Immunohistochemical Expression of Metastasis-Associated Gene 3 (MTA3) and Epithelial-Mesenchymal Transition (EMT) Markers in Colorectal Carcinoma: A Cross-sectional StudyAya Salah Ali Saad Rezk, Mohamed Alaa Mokhtar, Mohamed Ali Alrashidy, et al.Inorganic Chemistry|March 31, 2011
Syntheses, crystal structures, transport properties and first-principles electronic structure study of the (tTTF)2X (X=Br, I) low-dimensional antiferromagnetsMarc Fourmigué, Eric W Reinheimer, Ali Assaf, et al.Journal of Telemedicine and Telecare|March 28, 2025
Clinical decision support systems for heart failure management optimization: A systematic review and meta-analysis of randomized controlled trialsUbaid Khan, Ahmed Mazen Amin, Yehya Khlidj, et al.Hematological Oncology|February 14, 2008
Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in TunisiaAbir Gmidène, Hlima Sennana, Hatem Elghezal, et al.Thrombosis Research|March 7, 2026
Optimal antithrombotic strategies in atrial fibrillation patients undergoing PCI: A network meta-analysis of randomized trialsMustafa Abomohsen, Mohamed Rifai, Mohamed S Elgendy, et al.Molecular Cytogenetics|February 25, 2021
Disorders of sex development in Wolf-Hirschhorn syndrome: a genotype-phenotype correlation and MSX1 as candidate geneKhouloud Rjiba, Hédia Ayech, Olfa Kraiem, et al.Biochemical and Biophysical Research Communications|February 13, 2013
Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian manMyriam Ghorbel, Siwar Baklouti-Gargouri, Hatem ElGhazel, et al.Iranian Journal of Public Health|April 24, 2015
Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes MellitusAbdelbasset Amara, Ilhem Ben Charfeddine, Houda Ghédir, et al.European Journal of Medical Genetics|June 12, 2012
Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotoniaInesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, et al.Pageof 37