Literature DB >> 3589742

Case report 418: Multiple enchondromatosis (Ollier disease) with severe vertebral changes.

E M Azouz.   

Abstract

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Year:  1987        PMID： 3589742     DOI： 10.1007/bf00356960

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN： 0364-2348            Impact factor:   2.199


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  9 in total

1.  Spondylo-metaphyseal dysplasias (report of a case of common type and three pairs of siblings of new varieties).

Authors:  K Kozlowski; A Barylak; R W Middleton; M Rybakowa; P Thomas; J Walecki
Journal:  Australas Radiol       Date:  1976-06

2.  Metaphyseal chondrodysplasia calcificans. A report on two cases.

Authors:  S van Creveld; K Kozlowski; K Pietron; A van der Valk
Journal:  Br J Radiol       Date:  1971-10       Impact factor: 3.039

3.  The variable manifestations of multiple enchondromatosis.

Authors:  F Mainzer; H Minagi; H L Steinbach
Journal:  Radiology       Date:  1971-05       Impact factor: 11.105

4.  [Multiple chondroma affecting the spine: spondylo-enchondroplasia and other forms (author's transl)].

Authors:  J Sauvegrain; P Maroteaux; J Ribier; L Garel; L Tato; P Rochiccioli; J de Magalhaes; B Duhamel
Journal:  J Radiol       Date:  1980 Aug-Sep

5.  [Spondylo-enchondrodysplasia].

Authors:  S Chagnon; P Lacert; M Blery
Journal:  J Radiol       Date:  1985-01

6.  Generalized enchondromatosis with unusual complications of soft tissue calcifications and hemangiomas. Follow-up for over a twelve-year period.

Authors:  N Kaibara; M Mitsuyasu; I Katsuki; T Hotokebuchi; K Takagishi
Journal:  Skeletal Radiol       Date:  1982       Impact factor: 2.199

7.  Micromelic type of spondylo-meta-epiphyseal dysplasia.

Authors:  K Kozlowski
Journal:  Pediatr Radiol       Date:  1974-04-05

8.  Spondyloenchondrodysplasia. Enchondromatomosis with severe platyspondyly in two brothers.

Authors:  S Schorr; C Legum; M Ochshorn
Journal:  Radiology       Date:  1976-01       Impact factor: 11.105

9.  Two peculiar types of enchondromatosis.

Authors:  J Spranger; H Kemperdieck; H Bakowski; J M Opitz
Journal:  Pediatr Radiol       Date:  1978-12-04
  9 in total
  5 in total

1.  Longitudinal Follow-Up of Two Patients with Dysspondyloenchondromatosis due to Novel Heterozygous Mutations in COL2A1.

Authors:  Nilay Güneş; Gözde Yeşil; Kubilay Beng; Sinan Kahraman; Beyhan Tüysüz
Journal:  Mol Syndromol       Date:  2018-04-24

2.  Dysspondyloenchondromatosis in the newborn. Report of four cases.

Authors:  K Kozlowski; K Brostrom; J Kennedy; H Lange; L Morris
Journal:  Pediatr Radiol       Date:  1994

3.  Acroform type of enchondromatosis associated with severe vertebral involvement and facial dysmorphism in a boy with a new variant of enchondromatosis type I1 of Spranger: case report and a review of the literature.

Authors:  Ali Al Kaissi; Katharina Roetzer; Klaus Klaushofer; Franz Grill
Journal:  Cases J       Date:  2008-11-18

4.  Dysspondyloenchondromatosis: Another COL2A1-Related Skeletal Dysplasia?

Authors:  T Nakane; T Tando; K Aoyagi; K Hatakeyama; G Nishimura; I P J Coucke; G Mortier; K Sugita
Journal:  Mol Syndromol       Date:  2011-10-18

5.  Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey.

Authors:  Tracy A Briggs; Gillian I Rice; Navid Adib; Lesley Ades; Stephane Barete; Kannan Baskar; Veronique Baudouin; Ayse N Cebeci; Philippe Clapuyt; David Coman; Lien De Somer; Yael Finezilber; Moshe Frydman; Ayla Guven; Sébastien Heritier; Daniela Karall; Muralidhar L Kulkarni; Pierre Lebon; David Levitt; Martine Le Merrer; Agnes Linglart; John H Livingston; Vincent Navarro; Ericka Okenfuss; Anne Puel; Nicole Revencu; Sabine Scholl-Bürgi; Marina Vivarelli; Carine Wouters; Brigitte Bader-Meunier; Yanick J Crow
Journal:  J Clin Immunol       Date:  2016-03-08       Impact factor: 8.317
  5 in total

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