Publications by authors named "P Rondot"

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Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
Michèl A Willemsen, Marcel M Verbeek, Erik-Jan Kamsteeg, Johanneke F de Rijk-van Andel, Alec Aeby, Pierre Rondot

Brain· June 2010

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Idiopathic osteonecrosis of femur in adult Morquio type B disease.
Charles J Menkès, Pierre Rondot

J Rheumatol· November 2007

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G. B. A. Duchenne de Boulogne (1806-1875).
P Rondot

J Neurol· July 2005

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[Topography of secondary dystonia lesions].
P Rondot, N Bathien, P Tempier, D Fredy

Bull Acad Natl Med· December 2001

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Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonism.
R J Swaans, P Rondot, W O Renier, L P Van Den Heuvel, G C Steenbergen-Spanjers

Ann Hum Genet· January 2000

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