Literature DB >> 3706401

On congenital lymphedema.

J M Opitz.   

Abstract

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Year:  1986        PMID： 3706401     DOI： 10.1002/ajmg.1320240115

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  4 in total

1.  Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.

Authors:  A Irrthum; M J Karkkainen; K Devriendt; K Alitalo; M Vikkula
Journal:  Am J Hum Genet       Date:  2000-06-09       Impact factor: 11.025

2.  Case Report: Progressive central conducting lymphatic abnormalities in the RASopathies. Two case reports, including successful treatment by MEK inhibition.

Authors:  Kristiana Gordon; Matthew Moore; Malou Van Zanten; Julian Pearce; Maxim Itkin; Brendan Madden; Lakshmi Ratnam; Peter S Mortimer; Rani Nagaraja; Sahar Mansour
Journal:  Front Genet       Date:  2022-09-27       Impact factor: 4.772

3.  The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome.

Authors:  Sarah Joyce; Kristiana Gordon; Glen Brice; Pia Ostergaard; Rani Nagaraja; John Short; Sandra Moore; Peter Mortimer; Sahar Mansour
Journal:  Eur J Hum Genet       Date:  2015-08-05       Impact factor: 4.246

4.  Transient idiopathic primary penoscrotal edema.

Authors:  Sody A Namir; Akiva Trattner
Journal:  Indian J Dermatol       Date:  2013-09       Impact factor: 1.494
  4 in total

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