Literature DB >> 29893154

A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.

Chloé J Arthuis1, Mathilde Nizon2, Martin Kömhoff3, Bodo B Beck4,5, Vera Riehmer4, Tiphaine Bihouée6, Alexandra Bruel6, Nadir Benbrik7, Norbert Winer1, Bertrand Isidor2.   

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Year:  2018        PMID： 29893154     DOI： 10.1080/01443615.2018.1454415

Source DB:  PubMed          Journal:  J Obstet Gynaecol        ISSN： 0144-3615            Impact factor:   1.246


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  4 in total

Review 1.  Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical Importance.

Authors:  Laura Florea; Lavinia Caba; Eusebiu Vlad Gorduza
Journal:  Front Pediatr       Date:  2022-06-03       Impact factor: 3.569

2.  Transient Polyhydramnios during Pregnancy Complicated with Gestational Diabetes Mellitus: Case Report and Systematic Review.

Authors:  Agnesa Preda; Adela Gabriela Ștefan; Silviu Daniel Preda; Alexandru Cristian Comănescu; Mircea-Cătălin Forțofoiu; Mihaela Ionela Vladu; Maria Forțofoiu; Maria Moța
Journal:  Diagnostics (Basel)       Date:  2022-05-28

Review 3.  Pathophysiological aspects of the thick ascending limb and novel genetic defects: HELIX syndrome and transient antenatal Bartter syndrome.

Authors:  Rosa Vargas-Poussou
Journal:  Pediatr Nephrol       Date:  2021-03-17       Impact factor: 3.651

4.  A Case Report and Literature Review of a Novel Mutation in the MAGED2 Gene of a Patient With Severe Transient Polyhydramnios.

Authors:  Xiaoxia Wu; Le Huang; Caiqun Luo; Yang Liu; Jianmin Niu
Journal:  Front Pediatr       Date:  2021-12-01       Impact factor: 3.418
  4 in total

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