Literature DB >> 12976160

Familial and sporadic neurogenic acro-osteolysis.

L GIACCAI.   

Abstract

Entities:  

Keywords:  BONES/diseases; EXTREMITIES/diseases

Mesh：

Year:  1952        PMID： 12976160     DOI： 10.3109/00016925209177008

Source DB:  PubMed          Journal:  Acta radiol        ISSN： 0001-6926            Impact factor:   1.990


× No keyword cloud information.
  5 in total

1.  [ON A FAMILIAL DISEASE WITH AN UNUSUAL NEUROLOGIC SYMPTOM COMBINATION, OLIGOPHRENIA, DEMENTIA, MULTIPLE SKIN ULCERATIONS, SPLENOMEGALY AND AMINO ACID METABOLIC DISORDERS].

Authors:  J BRUCK; F GERSTENBRAND; P PROSENZ; R SANTLER; B SCHOBEL; F WEWALKA
Journal:  Dtsch Z Nervenheilkd       Date:  1964-02-21

2.  [Hereditary sensory neuropathy. I].

Authors:  G Lassmann; H Partsch
Journal:  Dtsch Z Nervenheilkd       Date:  1970

3.  [On the differential diagnosis of osteolytic processes].

Authors:  K H Schüler; W Laschner
Journal:  Arch Orthop Unfallchir       Date:  1969

4.  Hadju-Cheney syndrome. Report of a non-familial case.

Authors:  J Kawamura; K Matsubayashi; M Ogawa
Journal:  Neuroradiology       Date:  1981       Impact factor: 2.804

5.  Is an association of acro-osteolysis, bone fragility, and enchondromatosis a newfound disease caused by an amplification of PTHLH? A case report.

Authors:  Stéphane Echaubard; Céline Pebrel-Richard; Aurélie Chausset; Jean-Louis Kemeny; Etienne Merlin; Fanny Laffargue
Journal:  Pediatr Rheumatol Online J       Date:  2022-07-30       Impact factor: 3.413
  5 in total

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