Literature DB >> 19644134

The hereditary stomatocytoses.

Joanna F Flatt, Lesley J Bruce.   

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Year:  2009        PMID： 19644134      PMCID： PMC2719024          DOI： 10.3324/haematol.2009.010041

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  18 in total

Review 1.  Hemolytic disease due to membrane ion channel disorders.

Authors:  Gordon W Stewart
Journal:  Curr Opin Hematol       Date:  2004-07       Impact factor: 3.284

2.  A case of congenital dyserythropoietic anaemia with stomatocytosis, reduced bands 7 and 8 and normal cation content.

Authors:  O Olivieri; D Girelli; L Vettore; G Balercia; R Corrocher
Journal:  Br J Haematol       Date:  1992-02       Impact factor: 6.998

3.  Melanesian hereditary ovalocytes have a deletion in red cell band 3.

Authors:  M J Tanner; L Bruce; P G Martin; D M Rearden; G L Jones
Journal:  Blood       Date:  1991-11-15       Impact factor: 22.113

4.  South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cells.

Authors:  L J Bruce; S M Ring; K Ridgwell; D M Reardon; C A Seymour; H M Van Dort; P S Low; M J Tanner
Journal:  Biochim Biophys Acta       Date:  1999-01-12

5.  The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast.

Authors:  A M Marini; G Matassi; V Raynal; B André; J P Cartron; B Chérif-Zahar
Journal:  Nat Genet       Date:  2000-11       Impact factor: 38.330

6.  A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema.

Authors:  S Grootenboer; P O Schischmanoff; T Cynober; J C Rodrigue; J Delaunay; G Tchernia; J P Dommergues
Journal:  Br J Haematol       Date:  1998-11       Impact factor: 6.998

Review 7.  The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.

Authors:  Jean Delaunay
Journal:  Semin Hematol       Date:  2004-04       Impact factor: 3.851

8.  Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

Authors:  A Iolascon; G W Stewart; J F Ajetunmobi; S Perrotta; J Delaunay; M Carella; L Zelante; P Gasparini
Journal:  Blood       Date:  1999-05-01       Impact factor: 22.113

9.  The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.

Authors:  Britta Fricke; Annette C Argent; Margaret C Chetty; Arnold R Pizzey; E Jane Turner; Mei M Ho; Achille Iolascon; Monika von Düring; Gordon W Stewart
Journal:  Blood       Date:  2003-05-15       Impact factor: 22.113

10.  Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).

Authors:  M Carella; G Stewart; J F Ajetunmobi; S Perrotta; S Grootenboer; G Tchernia; J Delaunay; A Totaro; L Zelante; P Gasparini; A Iolascon
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025
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  4 in total

Review 1.  Disorders of erythrocyte hydration.

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

2.  Quantitative Models of Lipid Transfer and Membrane Contact Formation.

Authors:  Yongli Zhang; Jinghua Ge; Xin Bian; Avinash Kumar
Journal:  Contact (Thousand Oaks)       Date:  2022-05-04

3.  Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.

Authors:  Damien Barneaud-Rocca; Bernard Pellissier; Franck Borgese; Hélène Guizouarn
Journal:  Int J Cell Biol       Date:  2011-08-23

4.  [Clinical features of hereditary stomatocytosis: 12 cases report and literatures review].

Authors:  Y Q Shao; N Nie; J B Huang; Z D Huang; M L Ge; J Zhang; X X Li; J Shi; Y Z Zheng
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2017-07-14
  4 in total

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