Literature DB >> 17219391

Prenatal manifestation of pancytopenia in Pearson marrow-pancreas syndrome caused by a mitochondrial DNA deletion.

Almut Giese1, Renate Kirschner-Schwabe, Katharina Blumchen, Lena Wronski, Shabnam Shalapour, Javier Prada, Pablo Hernáiz Driever, Martin Brauer, Markus Schuelke, Günter Henze, Karl Seeger.   

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Year:  2007        PMID： 17219391     DOI： 10.1002/ajmg.a.31493

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  3 in total

Review 1.  Antenatal manifestations of inborn errors of metabolism: prenatal imaging findings.

Authors:  Laurent Guibaud; Sophie Collardeau-Frachon; Audrey Lacalm; Mona Massoud; Massimiliano Rossi; Marie Pierre Cordier; Christine Vianey-Saban
Journal:  J Inherit Metab Dis       Date:  2016-11-16       Impact factor: 4.982

2.  Case Report: Clinical and Genetic Characteristics of Pearson Syndrome in a Chinese Boy and 139 Patients.

Authors:  Yanqin Ying; Yan Liang; Xiaoping Luo; Ming Wei
Journal:  Front Genet       Date:  2022-05-23       Impact factor: 4.772

3.  Early neurological impairment and severe anemia in a newborn with Pearson syndrome.

Authors:  Anne-Sophie Morel; Nadia Joris; Reto Meuli; Sébastien Jacquemont; Diana Ballhausen; Luisa Bonafé; Sarah Fattet; Jean-François Tolsa
Journal:  Eur J Pediatr       Date:  2008-06-14       Impact factor: 3.183
  3 in total

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