Literature DB >> 18273584

[Nodular cutaneous papules and bone atrophy in infancy. Hereditary osteodysplasia pseudohypoparathyroidism, Albright-Syndrome]].

J Hepp1, G Hirschfeld, L Weber, T Weiss, K Scharfetter-Kochanek.   

Abstract

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Mesh：

Year:  2008        PMID： 18273584     DOI： 10.1007/s00105-007-1461-3

Source DB:  PubMed          Journal:  Hautarzt        ISSN： 0017-8470            Impact factor:   0.751


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  4 in total

Review 1.  Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.

Authors:  M D Ringel; W F Schwindinger; M A Levine
Journal:  Medicine (Baltimore)       Date:  1996-07       Impact factor: 1.889

2.  Treatment of primary miliary osteoma cutis with incision, curettage, and primary closure.

Authors:  J F Altman; K S Nehal; K J Busam; A C Halpern
Journal:  J Am Acad Dermatol       Date:  2001-01       Impact factor: 11.527

3.  Osteomas of the skin revisited: a clinicopathologic review of 74 cases.

Authors:  Phillip A Conlin; Laura P Jimenez-Quintero; Ronald P Rapini
Journal:  Am J Dermatopathol       Date:  2002-12       Impact factor: 1.533

4.  [Primary cutaneous osteoma in hereditary Albright osteodystrophy].

Authors:  K Diercks; K Schulte; H C Schuppe; P Lehmann
Journal:  Hautarzt       Date:  1996-09       Impact factor: 0.751
  4 in total

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