Literature DB >> 20091385

A case of congenital bone marrow failure with radio-ulnar synostosis.

Hisao Yoshida, Yoshiko Hashii, Tokuko Okuda, Shigenori Kusuki, Emiko Sato, Akiko Inoue, Chihiro Kawakami, Miharu Yabe, Hideaki Ohta, Keiichi Ozono.   

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Year:  2010        PMID： 20091385     DOI： 10.1007/s12185-010-0494-z

Source DB:  PubMed          Journal:  Int J Hematol        ISSN： 0925-5710            Impact factor:   2.490


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  10 in total

Review 1.  Congenital bone marrow failure syndromes.

Authors:  C A Sieff; E Nisbet-Brown; D G Nathan
Journal:  Br J Haematol       Date:  2000-10       Impact factor: 6.998

2.  Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation.

Authors:  A A Thompson; L T Nguyen
Journal:  Nat Genet       Date:  2000-12       Impact factor: 38.330

Review 3.  Hox genes in hematopoiesis and leukemogenesis.

Authors:  B Argiropoulos; R K Humphries
Journal:  Oncogene       Date:  2007-10-15       Impact factor: 9.867

4.  Genetic interactions of Hox genes in limb development: learning from compound mutants.

Authors:  F M Rijli; P Chambon
Journal:  Curr Opin Genet Dev       Date:  1997-08       Impact factor: 5.578

5.  Thrombocytopenia-absent radius syndrome: a clinical genetic study.

Authors:  K L Greenhalgh; R T Howell; A Bottani; P J Ancliff; H G Brunner; C C Verschuuren-Bemelmans; E Vernon; K W Brown; R A Newbury-Ecob
Journal:  J Med Genet       Date:  2002-12       Impact factor: 6.318

6.  Late onset bone marrow failure associated with proximal fusion of radius and ulna: a new syndrome.

Authors:  I Dokal; P Ganly; I Riebero; J Marsh; A Steed; J Kendra; C Drysdale; J Hows
Journal:  Br J Haematol       Date:  1989-02       Impact factor: 6.998

Review 7.  Congenital hypoplastic anemia.

Authors:  L K Diamond; W C Wang; B P Alter
Journal:  Adv Pediatr       Date:  1976

8.  Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome.

Authors:  A A Thompson; K Woodruff; S A Feig; L T Nguyen; N C Schanen
Journal:  Br J Haematol       Date:  2001-06       Impact factor: 6.998

Review 9.  Limb malformations and the human HOX genes.

Authors:  Frances R Goodman
Journal:  Am J Med Genet       Date:  2002-10-15

10.  Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton.

Authors:  B Favier; F M Rijli; C Fromental-Ramain; V Fraulob; P Chambon; P Dollé
Journal:  Development       Date:  1996-02       Impact factor: 6.868
  10 in total
  3 in total

1.  Bone marrow morphology and disease progression in congenital thrombocytopenia: a detailed clinicopathologic and genetic study of eight cases.

Authors:  Hamilton C Tsang; James B Bussel; Susan Mathew; Yen-Chun Liu; Allison A Imahiyerobo; Attilio Orazi; Julia T Geyer
Journal:  Mod Pathol       Date:  2017-01-06       Impact factor: 7.842

2.  MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.

Authors:  Manuela Germeshausen; Phil Ancliff; Jaime Estrada; Markus Metzler; Eva Ponstingl; Horst Rütschle; Dirk Schwabe; Richard H Scott; Sule Unal; Angela Wawer; Bernward Zeller; Matthias Ballmaier
Journal:  Blood Adv       Date:  2018-03-27

3.  Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.

Authors:  Tetsuya Niihori; Meri Ouchi-Uchiyama; Yoji Sasahara; Takashi Kaneko; Yoshiko Hashii; Masahiro Irie; Atsushi Sato; Yuka Saito-Nanjo; Ryo Funayama; Takeshi Nagashima; Shin-Ichi Inoue; Keiko Nakayama; Keiichi Ozono; Shigeo Kure; Yoichi Matsubara; Masue Imaizumi; Yoko Aoki
Journal:  Am J Hum Genet       Date:  2015-11-12       Impact factor: 11.025
  3 in total

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