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Showing results (111-120 of 122) with videos related to

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Oncogene|September 22, 2010
Vimentin is a novel AKT1 target mediating motility and invasionQ-S Zhu, K Rosenblatt, K-L Huang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 30, 2015
Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis?Z Leibovitz, E Daniel-Spiegel, G Malinger, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 14, 2011
A nonrandom association of gastrointestinal stromal tumor (GIST) and desmoid tumor (deep fibromatosis): case series of 28 patientsA G Dumont, L Rink, A K Godwin, et al.
European Journal of Medical Genetics|November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcomeB Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Oncogene|January 13, 2015
NKD2, a negative regulator of Wnt signaling, suppresses tumor growth and metastasis in osteosarcomaS Zhao, L Kurenbekova, Y Gao, et al.
American Journal of Human Genetics|March 20, 2001
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plusR H Wallace, I E Scheffer, S Barnett, et al.
AJNR. American Journal of Neuroradiology|February 23, 2023
Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem MalformationM Gafner, C Garel, Z Leibovitz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 12, 2019
Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite JewsM Weisz-Hubshman, H Meirson, R Michaelson-Cohen, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 4, 2021
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomalyK Krajden Haratz, P Oliveira Szejnfeld, M Govindaswamy, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Oncogene|September 22, 2010
Vimentin is a novel AKT1 target mediating motility and invasionQ-S Zhu, K Rosenblatt, K-L Huang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 30, 2015
Prediction of microcephaly at birth using three reference ranges for fetal head circumference: can we improve prenatal diagnosis?Z Leibovitz, E Daniel-Spiegel, G Malinger, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 14, 2011
A nonrandom association of gastrointestinal stromal tumor (GIST) and desmoid tumor (deep fibromatosis): case series of 28 patientsA G Dumont, L Rink, A K Godwin, et al.
European Journal of Medical Genetics|November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcomeB Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Oncogene|January 13, 2015
NKD2, a negative regulator of Wnt signaling, suppresses tumor growth and metastasis in osteosarcomaS Zhao, L Kurenbekova, Y Gao, et al.
American Journal of Human Genetics|March 20, 2001
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plusR H Wallace, I E Scheffer, S Barnett, et al.
AJNR. American Journal of Neuroradiology|February 23, 2023
Medullary Tegmental Cap Dysplasia: Fetal and Postnatal Presentations of a Unique Brainstem MalformationM Gafner, C Garel, Z Leibovitz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 12, 2019
Novel WWOX deleterious variants cause early infantile epileptic encephalopathy, severe developmental delay and dysmorphism among Yemenite JewsM Weisz-Hubshman, H Meirson, R Michaelson-Cohen, et al.
Molecular Syndromology|May 9, 2013
Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 MutationsM Alders, A Mendola, L Adès, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 4, 2021
Prenatal diagnosis of rhombencephalosynapsis: neuroimaging features and severity of vermian anomalyK Krajden Haratz, P Oliveira Szejnfeld, M Govindaswamy, et al.
Pageof 13