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Gustavo Malinger

Showing results (71-80 of 97) with videos related to

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Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|July 5, 2018
Ultrasound Nomograms of the Fetal Optic Nerve Sheath DiameterKarina Krajden Haratz, Yaakov Melcer, Zvi Leibovitz, et al.
Prenatal Diagnosis|December 7, 2025
Fetal Macrocephaly: Prenatal Findings and Follow-Up in Cases With High Risk for Abnormal OutcomeHadas Miremberg, Gustavo Malinger, Deborah Kidron, et al.
Radiology|February 9, 2013
Human long bone development in vivo: analysis of the distal femoral epimetaphysis on MR images of fetusesUrsula Nemec, Stefan F Nemec, Michael Weber, et al.
European Journal of Human Genetics : EJHG|April 10, 2021
Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestationsMoran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, et al.
Fetal Diagnosis and Therapy|June 19, 2017
Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRIKarina Krajden Haratz, Alon Peled, Boris Weizman, et al.
Translational Pediatrics|January 24, 2022
Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the <i>HNF1B</i> geneRoxana Cleper, Adi Reches, Dana Shapira, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsEsther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Fetal Diagnosis and Therapy|February 4, 2024
Clinical Practice Guidelines and Recommendations by the World Association of Perinatal Medicine and Perinatal Medicine Foundation: Reporting Suspected Findings from Fetal Central Nervous System ExaminationValentina De Robertis, Cihat Sen, Ilan Timor-Tritsch, et al.
Developmental Medicine and Child Neurology|March 29, 2025
Neurodevelopmental outcome of perinatal intracranial haemorrhage in patients born at term: A prospective studyStephanie Libzon, Shelly I Shiran, Aviva Fattal-Valevski, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 15, 2018
Fetal pericallosal lipomas - Clues to diagnosis in the second trimesterShiri Shinar, Tally Lerman-Sagie, Monica Echevarria Telleria, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|July 5, 2018
Ultrasound Nomograms of the Fetal Optic Nerve Sheath DiameterKarina Krajden Haratz, Yaakov Melcer, Zvi Leibovitz, et al.
Prenatal Diagnosis|December 7, 2025
Fetal Macrocephaly: Prenatal Findings and Follow-Up in Cases With High Risk for Abnormal OutcomeHadas Miremberg, Gustavo Malinger, Deborah Kidron, et al.
Radiology|February 9, 2013
Human long bone development in vivo: analysis of the distal femoral epimetaphysis on MR images of fetusesUrsula Nemec, Stefan F Nemec, Michael Weber, et al.
European Journal of Human Genetics : EJHG|April 10, 2021
Deletion in COL4A2 is associated with a three-generation variable phenotype: from fetal to adult manifestationsMoran Hausman-Kedem, Liat Ben-Sira, Debora Kidron, et al.
Fetal Diagnosis and Therapy|June 19, 2017
Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRIKarina Krajden Haratz, Alon Peled, Boris Weizman, et al.
Translational Pediatrics|January 24, 2022
Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the <i>HNF1B</i> geneRoxana Cleper, Adi Reches, Dana Shapira, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsEsther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
Fetal Diagnosis and Therapy|February 4, 2024
Clinical Practice Guidelines and Recommendations by the World Association of Perinatal Medicine and Perinatal Medicine Foundation: Reporting Suspected Findings from Fetal Central Nervous System ExaminationValentina De Robertis, Cihat Sen, Ilan Timor-Tritsch, et al.
Developmental Medicine and Child Neurology|March 29, 2025
Neurodevelopmental outcome of perinatal intracranial haemorrhage in patients born at term: A prospective studyStephanie Libzon, Shelly I Shiran, Aviva Fattal-Valevski, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 15, 2018
Fetal pericallosal lipomas - Clues to diagnosis in the second trimesterShiri Shinar, Tally Lerman-Sagie, Monica Echevarria Telleria, et al.
Pageof 10