Literature DB >> 31256860

Posterior Fossa Malformations.

Mariasavina Severino1, Thierry A G M Huisman2.   

Abstract

This article discusses the normal anatomy of the posterior fossa structures followed by a discussion of the characteristic neuroimaging features of a variety of cerebellar and brainstem malformations. In this context, the authors classify posterior fossa malformations based on the neuroimaging pattern into (1) predominantly cerebellar, (2) cerebellar and brainstem, and (3) predominantly brainstem malformations.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Brain stem; Cerebellum; Children; DTI; MR imaging; Malformations; Midbrain-hindbrain; Neuroimaging

Mesh：

Year:  2019        PMID： 31256860     DOI： 10.1016/j.nic.2019.03.008

Source DB:  PubMed          Journal:  Neuroimaging Clin N Am        ISSN： 1052-5149            Impact factor:   2.264


  5 in total

1.  Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development.

Authors:  Andrea Accogli; Shenzhao Lu; Ilaria Musante; Paolo Scudieri; Jill A Rosenfeld; Mariasavina Severino; Simona Baldassari; Michele Iacomino; Antonella Riva; Ganna Balagura; Gianluca Piccolo; Carlo Minetti; Denis Roberto; Fan Xia; Razaali Razak; Emily Lawrence; Mohamed Hussein; Emmanuel Yih-Herng Chang; Michelle Holick; Elisa Calì; Emanuela Aliberto; Rosalba De-Sarro; Antonio Gambardella; Undiagnosed Diseases Network; SYNaPS Study Group; Lisa Emrick; Peter J A McCaffery; Margaret Clagett-Dame; Paul C Marcogliese; Hugo J Bellen; Seema R Lalani; Federico Zara; Pasquale Striano; Vincenzo Salpietro
Journal:  Cerebellum       Date:  2022-02-26       Impact factor: 3.847

Review 2.  Fetal Brain Development: Regulating Processes and Related Malformations.

Authors:  Zvi Leibovitz; Tally Lerman-Sagie; Leila Haddad
Journal:  Life (Basel)       Date:  2022-05-29

Review 3.  Imaging spectrum of posterior fossa anomalies on foetal magnetic resonance imaging with an algorithmic approach to diagnosis.

Authors:  Harsha Vardhan Mahalingam; Rajeswaran Rangasami; Suresh Seshadri; Indrani Suresh
Journal:  Pol J Radiol       Date:  2021-03-30

4.  L1CAM variants cause two distinct imaging phenotypes on fetal MRI.

Authors:  Andrea Accogli; Stacy Goergen; Giana Izzo; Kshitij Mankad; Karina Krajden Haratz; Cecilia Parazzini; Michael Fahey; Lara Menzies; Julia Baptista; Lucia Carpineta; Domenico Tortora; Ezio Fulcheri; Valerio Gaetano Vellone; Dario Paladini; Luigina Spaccini; Valentina Toto; Claire Trayers; Liat Ben Sira; Adi Reches; Gustavo Malinger; Vincenzo Salpietro; Patrizia De Marco; Myriam Srour; Federico Zara; Valeria Capra; Andrea Rossi; Mariasavina Severino
Journal:  Ann Clin Transl Neurol       Date:  2021-09-12       Impact factor: 4.511

5.  SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum.

Authors:  Valentina Serpieri; Fulvio D'Abrusco; Jennifer C Dempsey; Yong-Han Hank Cheng; Filippo Arrigoni; Janice Baker; Roberta Battini; Enrico Silvio Bertini; Renato Borgatti; Angela K Christman; Cynthia Curry; Stefano D'Arrigo; Joel Fluss; Michael Freilinger; Simone Gana; Gisele E Ishak; Vincenzo Leuzzi; Hailey Loucks; Filippo Manti; Nancy Mendelsohn; Laura Merlini; Caitlin V Miller; Ansar Muhammad; Sara Nuovo; Romina Romaniello; Wolfgang Schmidt; Sabrina Signorini; Sabrina Siliquini; Krzysztof Szczałuba; Gessica Vasco; Meredith Wilson; Ginevra Zanni; Eugen Boltshauser; Dan Doherty; Enza Maria Valente
Journal:  J Med Genet       Date:  2021-10-21       Impact factor: 5.941
  5 in total

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