P Rondot
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Explore the profile of P Rondot including associated specialties, affiliations and a list of published articles.
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Recent Articles
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Rondot P, BATHIEN N, Tempier P, Fredy D
Bull Acad Natl Med
. 2001 Jul;
185(1):103-4; discussion 114-7.
PMID: 11474562
Biological causes provoking dystonia can not be systematized, with the exception of the small group of levodopa-responsive dystonia. Therefore the pathophysiology of the dystonic syndrome can be approached by considering...
3.
Swaans R, Rondot P, Renier W, van den Heuvel L, Wevers R
Ann Hum Genet
. 2001 Mar;
64(Pt 1):25-31.
PMID: 11246459
Mutation detection in the tyrosine hydroxylase gene (TH) was performed in patients from two families. DNA sequencing revealed the presence of four novel missense mutations (exon 9 and 14 in...
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Ziegler M, Rondot P
Presse Med
. 1999 Oct;
28(26):1414-8.
PMID: 10518963
Objectives: Several controlled trials have shown that Trivastal (piribedil), a direct dopamine agonist, is active in the treatment of Parkinson's disease. The aim of the present clinical trial was to...
6.
Rondot P, Wevers R
Bull Acad Natl Med
. 1999 Aug;
183(3):639-46; discussion 646-7.
PMID: 10437291
The cause of Dystonia Musculorum Deformans (DMD) is most frequently unknown, therefore the treatment can only be symptomatic and often disappointing. In 1971 we reported the first two cases of...
7.
Potagas C, Dellatolas G, Ziegler M, LEVETEAU J, BATHIEN N, MAC LEOD P, et al.
Mov Disord
. 1998 Jun;
13(3):394-9.
PMID: 9613727
We used two simple tasks to test the capacities of patients with Parkinson's disease to discriminate and identify olfactory stimuli. The patients presented defective odor identification abilities whereas their capacity...
8.
Navon R, Khosravi R, Melki J, Drucker L, Fontaine B, Turpin J, et al.
Ann Neurol
. 1997 May;
41(5):631-8.
PMID: 9153525
Progressive proximal muscle weakness is present both in spinal muscular atrophy (SMA) type III (Kugelberg-Welander disease) and in GM2 gangliosidosis, diseases that segregate in an autosomal recessive fashion. The SMN...
9.
Rondot P, Navon R, Eymard B, Fardeau M, Turpin J, Lefevre M, et al.
Rev Neurol (Paris)
. 1997 Mar;
153(2):120-3.
PMID: 9296123
GM2 gangliosidosis are caused by a beta-hexosaminidase A enzyme deficiency. Mutations in the gene leaving residual enzyme activity give rise to juvenile and adult forms of the disease which have...
10.
Navon R, Khosravi R, Korczyn T, Masson M, Sonnino S, Fardeau M, et al.
Neurology
. 1995 Mar;
45(3 Pt 1):539-43.
PMID: 7898712
We describe two adult siblings who had had mild GM2 gangliosidosis since childhood. They presented with spinal muscular atrophy and dysarthria, and one sibling also had mental disturbances. Laboratory studies...