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Kalthoum Tlili-Graiess

Showing results (1-10 of 8) with videos related to

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Brain & Development|November 17, 2020
Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patientsSara Alharbi, Amal Alhashem, Fowzan Alkuraya, et al.
Pediatric Radiology|December 17, 2013
PHACES syndrome associated with carcinoid endobronchial tumorNadia Mama, Dorra H'mida, Imen Lahmar, et al.
Pediatric Neurology|November 28, 2018
Novel Homozygous Mutation of the AIMP1 Gene: A Milder Neuroimaging Phenotype With Preservation of the Deep White MatterAhmed BoAli, Kalthoum Tlili-Graiess, Amal AlHashem, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|November 19, 2013
Diffusion weighted MR imaging and proton MR spectroscopy findings of central neurocytoma with pathological correlationKalthoum Tlili-Graiess, Nadia Mama, Nadia Arifa, et al.
Clinical Imaging|January 14, 2014
Duodenal adenocarcinoma presenting as a mass with aneurismal dilatationNadia Mama, Aïda Ben Slama, Nadia Arifa, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndromeHeeba Y AlKalaf, Amal M AlHashem, Norah S AlSaleh, et al.
Journal of Medical Genetics|April 6, 2021
Mutations in phospholipase C eta-1 (<i>PLCH1</i>) are associated with holoprosencephalyIchrak Drissi, Emily Fletcher, Ranad Shaheen, et al.
American Journal of Human Genetics|November 19, 2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental AbnormalitiesLaura V Vandervore, Rachel Schot, Chiara Milanese, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Brain & Development|November 17, 2020
Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patientsSara Alharbi, Amal Alhashem, Fowzan Alkuraya, et al.
Pediatric Radiology|December 17, 2013
PHACES syndrome associated with carcinoid endobronchial tumorNadia Mama, Dorra H'mida, Imen Lahmar, et al.
Pediatric Neurology|November 28, 2018
Novel Homozygous Mutation of the AIMP1 Gene: A Milder Neuroimaging Phenotype With Preservation of the Deep White MatterAhmed BoAli, Kalthoum Tlili-Graiess, Amal AlHashem, et al.
Journal of Neuroradiology = Journal De Neuroradiologie|November 19, 2013
Diffusion weighted MR imaging and proton MR spectroscopy findings of central neurocytoma with pathological correlationKalthoum Tlili-Graiess, Nadia Mama, Nadia Arifa, et al.
Clinical Imaging|January 14, 2014
Duodenal adenocarcinoma presenting as a mass with aneurismal dilatationNadia Mama, Aïda Ben Slama, Nadia Arifa, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 1, 2020
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndromeHeeba Y AlKalaf, Amal M AlHashem, Norah S AlSaleh, et al.
Journal of Medical Genetics|April 6, 2021
Mutations in phospholipase C eta-1 (<i>PLCH1</i>) are associated with holoprosencephalyIchrak Drissi, Emily Fletcher, Ranad Shaheen, et al.
American Journal of Human Genetics|November 19, 2019
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental AbnormalitiesLaura V Vandervore, Rachel Schot, Chiara Milanese, et al.
Pageof 1