Literature DB >> 25332669

Case 1: An 18-month-old female infant with pancytopenia and hepatosplenomegaly.

Samin Alavi1, Nahid Arabi1.   

Abstract

Entities:  

Year:  2014        PMID： 25332669      PMCID： PMC4173899          DOI： 10.1093/pch/19.7.347

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN： 1205-7088            Impact factor:   2.253


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  2 in total

Review 1.  Osteopetrosis.

Authors:  Jakub Tolar; Steven L Teitelbaum; Paul J Orchard
Journal:  N Engl J Med       Date:  2004-12-30       Impact factor: 91.245

Review 2.  Osteopetrosis.

Authors:  Zornitza Stark; Ravi Savarirayan
Journal:  Orphanet J Rare Dis       Date:  2009-02-20       Impact factor: 4.123
  2 in total
  1 in total

1.  Progressive skeletal defects caused by Kindlin3 deficiency, a model of autosomal recessive osteopetrosis in humans.

Authors:  Tejasvi Dudiki; Daniel W Nascimento; Lauren S Childs; Swetha Kareti; Charlie Androjna; Irina Zhevlakova; Tatiana V Byzova
Journal:  Bone       Date:  2022-03-25       Impact factor: 4.626
  1 in total

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