Pierre Maroteaux - bibliography
Related eponyms
- Arkless-Graham syndrome
- Koslowski's syndrome
- Lamy-Maroteaux syndrome
- Maroeteaux-Lamy syndrome I
- Maroteaux's MEDTS syndrome
- Maroteaux's syndrome I
- Maroteaux's syndrome II
- Maroteaux-Lamy syndrome II
- Maroteaux-Lamy syndrome III
- Maroteaux-Lamy syndrome IV
- Maroteaux-Spranger-Wiedemann syndrome
Biography
French paediatrician, born 1926, Versailles.
Bibliography
- Les maladies osseuses de l'enfant.
With Clement Fauré, Claude Fessard and Pierre Rigault.
Foreword by Maurice Lamy.
In the series: Flammarion médecine-sciences.
1974. 1982. 3rd edition, 619 pages, 1995.
4th edition, 482 pages, by Pierre Maroteaux and Martine Le Merrer. 2002. - Bone diseases of children.
With Clement Fauré, Claude Fessard and Pierre Rigault.
A translation of: Les maladies osseuses de l'enfant.
Translated and adopted by Herbert J. Kaufmann.
Philadelphia : Lippincott, 1979, 17 + 435 pages. - Les formes pseudoachondroplastiques des dysplasies spondyloepiphysaires.
P. Maroteaux, M. Lamy.
La presse médicale, Paris, 1959, 67: 383-386. - Hydrocephalus and achondroplasia. A study of 25 observations.
A. Pierre-Kahn, J. F. Hirsch, D. Renier, J. Metzger, P. Maroteaux.
Child's Brain, 1980, 7: 205-19 - Bone Disorders of Children.
Oxford Monographs of Medical Genetics, No 23, 1993. - Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
F. Rousseau, J. Bonaventure, L. Legeai-Mallet, A. Pelet, J. M. Rozet, P. Maroteaux, M. LeMerrer, and A. Munnich.
Nature, London, 1994, 371: 252-254. - Cerebro-costo-mandibular syndrome: a follow-up study with 6 patients.
C. Schrander-Stumpel C, S. van der Meer, C. de Die-Smulders, P. Meinecke, E. Rupprecht, P. Maroteaux, J. Schranders, J. P. Fryns.
Genetic Counseling, 1996, 7: 71-72 - Mutations of the fibroblast growth factor receptor-3 gene in achondroplasia.
F. Rousseau, J. Bonaventure, L. Legeai-Mallet, A. Pelet, J. M. Rozet, P. Maroteaux, M. LeMerrer, and A. Munnich,.
Hormone Research, 1996, 45:108-110. - An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses.
Laurence Legeai-Mallet, Patricia Margaritte-Jeannin, Mohamed Lemdani, M. Le Merrer, Henry Plauchu, Pierre Maroteaux, A. Munnich, Françoise Clerget-Darpoux.
Human Genetics, Berlin, 1997, Volume 99 Issue 3, pp 298-302. - Presentation of six cases of Stüve-Wiedemann syndrome.
Valérie Cormier-Daire, A. Munnich, Stanislas Lyonnet, Pierre Rustin, Anne-Lise Delezoide, Pierre Maroteaux, Martine Le Merrer.
Pediatric Radiology, Berlin, 1998, Volume 28 Issue 10, pp 776-780.
