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Marianna Bugiani

Showing results (51-60 of 152) with videos related to

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BMC Gastroenterology|October 21, 2018
Transplantation, gene therapy and intestinal pathology in MNGIE patients and miceRana Yadak, Max V Boot, Niek P van Til, et al.
Molecular Therapy. Methods & Clinical Development|March 23, 2022
<i>In vivo</i> targeting of a variant causing vanishing white matter using CRISPR/Cas9Anne E J Hillen, Martina Hruzova, Tanja Rothgangl, et al.
Oncotarget|November 8, 2017
Trimethylation of H3K27 during human cerebellar development in relation to medulloblastomaShahryar E Mir, Michiel Smits, Dennis Biesmans, et al.
Circulation. Cardiovascular Imaging|July 15, 2024
Constrictive Pericarditis Caused by Primary Pericardial Mesothelioma: A Case SeriesTimion A Meijs, Josephine F Heidendael, Bernadette Schurink, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 23, 2018
Increased prevalence of abnormal vertebral patterning in fetuses and neonates with trisomy 21Pauline C Schut, Clara M A Ten Broek, Titia E Cohen-Overbeek, et al.
Frontiers in Medicine|January 5, 2024
Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation techniqueSilvia Storoni, Sara J E Verdonk, Dimitra Micha, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 2024
Case Series of 6 Fetuses With Osteogenesis Imperfecta Type II: A Retrospective Study of Heart PathologySara J E Verdonk, Silvia Storoni, Lidiia Zhytnik, et al.
Neurobiology of Disease|February 7, 2026
Astrocyte-specific deletion of LRRC8A causes neurological dysfunction but not chronic white matter edemaSven Kerst, Leoni Hoogterp, Marjolein Breur, et al.
Acta Neuropathologica Communications|June 22, 2023
Regional vulnerability of brain white matter in vanishing white matterJodie H K Man, Charlotte A G H van Gelder, Marjolein Breur, et al.
American Journal of Medical Genetics. Part A|May 5, 2021
Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous caseLuc Bruyndonckx, Judith L Vogelzang, Marianna Bugiani, et al.
Pageof 16

Showing results (51-60 of 152) with videos related to

Sort By:
Pageof 16
BMC Gastroenterology|October 21, 2018
Transplantation, gene therapy and intestinal pathology in MNGIE patients and miceRana Yadak, Max V Boot, Niek P van Til, et al.
Molecular Therapy. Methods & Clinical Development|March 23, 2022
<i>In vivo</i> targeting of a variant causing vanishing white matter using CRISPR/Cas9Anne E J Hillen, Martina Hruzova, Tanja Rothgangl, et al.
Oncotarget|November 8, 2017
Trimethylation of H3K27 during human cerebellar development in relation to medulloblastomaShahryar E Mir, Michiel Smits, Dennis Biesmans, et al.
Circulation. Cardiovascular Imaging|July 15, 2024
Constrictive Pericarditis Caused by Primary Pericardial Mesothelioma: A Case SeriesTimion A Meijs, Josephine F Heidendael, Bernadette Schurink, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 23, 2018
Increased prevalence of abnormal vertebral patterning in fetuses and neonates with trisomy 21Pauline C Schut, Clara M A Ten Broek, Titia E Cohen-Overbeek, et al.
Frontiers in Medicine|January 5, 2024
Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation techniqueSilvia Storoni, Sara J E Verdonk, Dimitra Micha, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 2024
Case Series of 6 Fetuses With Osteogenesis Imperfecta Type II: A Retrospective Study of Heart PathologySara J E Verdonk, Silvia Storoni, Lidiia Zhytnik, et al.
Neurobiology of Disease|February 7, 2026
Astrocyte-specific deletion of LRRC8A causes neurological dysfunction but not chronic white matter edemaSven Kerst, Leoni Hoogterp, Marjolein Breur, et al.
Acta Neuropathologica Communications|June 22, 2023
Regional vulnerability of brain white matter in vanishing white matterJodie H K Man, Charlotte A G H van Gelder, Marjolein Breur, et al.
American Journal of Medical Genetics. Part A|May 5, 2021
Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous caseLuc Bruyndonckx, Judith L Vogelzang, Marianna Bugiani, et al.
Pageof 16