Literature DB >> 8652859

Xerocytosis with concomitant intrauterine ascites: first description and therapeutic approach.

M Entezami, R Becker, H D Menssen, M Marcinkowski, H T Versmold.   

Abstract

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Year:  1996        PMID： 8652859

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  9 in total

Review 1.  Disorders of erythrocyte hydration.

Authors:  Patrick G Gallagher
Journal:  Blood       Date:  2017-10-19       Impact factor: 22.113

2.  A Novel Homozygous Missense Mutation of PIEZO1 Leading to Lymphatic Malformation-6 Identified in a Family With Three Adverse Pregnancy Outcomes due to Nonimmune Fetal Hydrops.

Authors:  Shuai Han; Xin Guo; Xiaogang Wang; Huijun Lin; Yiqi Yu; Jing Shu; Minyue Dong; Liwei Yang
Journal:  Front Genet       Date:  2022-05-13       Impact factor: 4.772

Review 3.  Erythrocyte disorders in the perinatal period.

Authors:  Laurie A Steiner; Patrick G Gallagher
Journal:  Semin Perinatol       Date:  2007-08       Impact factor: 3.300

Review 4.  Human phenotypes caused by PIEZO1 mutations; one gene, two overlapping phenotypes?

Authors:  Silvia Martin-Almedina; Sahar Mansour; Pia Ostergaard
Journal:  J Physiol       Date:  2018-01-31       Impact factor: 5.182

5.  Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.

Authors:  Elisa Fermo; Cristina Vercellati; Anna Paola Marcello; Anna Zaninoni; Richard van Wijk; Nadia Mirra; Cristina Curcio; Agostino Cortelezzi; Alberto Zanella; Wilma Barcellini; Paola Bianchi
Journal:  Case Rep Hematol       Date:  2017-03-06

Review 6.  The Molecular Basis for Altered Cation Permeability in Hereditary Stomatocytic Human Red Blood Cells.

Authors:  Joanna F Flatt; Lesley J Bruce
Journal:  Front Physiol       Date:  2018-04-16       Impact factor: 4.566

7.  Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.

Authors:  Véronique Picard; Corinne Guitton; Isabelle Thuret; Christian Rose; Laurence Bendelac; Kaldoun Ghazal; Patricia Aguilar-Martinez; Catherine Badens; Claire Barro; Claire Bénéteau; Claire Berger; Pascal Cathébras; Eric Deconinck; Jacques Delaunay; Jean-Marc Durand; Nadia Firah; Frédéric Galactéros; Bertrand Godeau; Xavier Jaïs; Jean-Pierre de Jaureguiberry; Camille Le Stradic; François Lifermann; Robert Maffre; Gilles Morin; Julien Perrin; Valérie Proulle; Marc Ruivard; Fabienne Toutain; Agnès Lahary; Loïc Garçon
Journal:  Haematologica       Date:  2019-01-17       Impact factor: 9.941

8.  Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia.

Authors:  Viktor Lukacs; Jayanti Mathur; Rong Mao; Pinar Bayrak-Toydemir; Melinda Procter; Stuart M Cahalan; Helen J Kim; Michael Bandell; Nicola Longo; Ronald W Day; David A Stevenson; Ardem Patapoutian; Bryan L Krock
Journal:  Nat Commun       Date:  2015-09-21       Impact factor: 14.919

9.  Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis.

Authors:  Elisavet Fotiou; Silvia Martin-Almedina; Michael A Simpson; Shin Lin; Kristiana Gordon; Glen Brice; Giles Atton; Iona Jeffery; David C Rees; Cyril Mignot; Julie Vogt; Tessa Homfray; Michael P Snyder; Stanley G Rockson; Steve Jeffery; Peter S Mortimer; Sahar Mansour; Pia Ostergaard
Journal:  Nat Commun       Date:  2015-09-03       Impact factor: 14.919
  9 in total

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