Literature DB >> 13605621

Fragilitas ossium hereditaria tarda: Ekman-Lobstein disease.

A CANIGGIA, C STUART, R GUIDERI.   

Abstract

Entities:  

Keywords:  OSTEOGENESIS IMPERFECTA

Mesh:

Year:  1958        PMID: 13605621

Source DB:  PubMed          Journal:  Acta Med Scand Suppl        ISSN: 0365-463X


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  5 in total

1.  [Pathogenetic problems in osteogenesis imperfecta].

Authors:  J J BETHGE
Journal:  Klin Wochenschr       Date:  1962-06-01

2.  [Blood studies in osteogenesis imperfecta].

Authors:  J F BETHGE
Journal:  Klin Wochenschr       Date:  1962-06-01

3.  Calcitonin treatment in Ekman-Lobstein disease.

Authors:  A Caniggia; C Gennari
Journal:  Calcif Tissue Res       Date:  1972

4.  Genetic heterogeneity in osteogenesis imperfecta.

Authors:  D O Sillence; A Senn; D M Danks
Journal:  J Med Genet       Date:  1979-04       Impact factor: 6.318

Review 5.  Osteogenesis imperfecta: clinical diagnosis, nomenclature and severity assessment.

Authors:  F S Van Dijk; D O Sillence
Journal:  Am J Med Genet A       Date:  2014-04-08       Impact factor: 2.802

  5 in total

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