Pierre-Yves Jeannet
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Explore the profile of Pierre-Yves Jeannet including associated specialties, affiliations and a list of published articles.
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29
Citations
1156
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Recent Articles
11.
Ganea R, Jeannet P, Paraschiv-Ionescu A, Goemans N, Piot C, Van den Hauwe M, et al.
J Child Neurol
. 2011 Jul;
27(1):30-8.
PMID: 21765150
The aim of this study was to investigate the alteration of the gait pattern in 25 children with Duchenne muscular dystrophy, using body-worn inertial sensors during a long walking distance....
12.
Lebon S, Maeder P, Maeder-Ingvar M, Poloni C, Mayor-Dubois C, Roulet-Perez E, et al.
Eur J Paediatr Neurol
. 2011 Jun;
15(6):544-6.
PMID: 21632267
Background: Subacute sclerosing panencephalitis (SSPE) is a rare and severe long-term complication of measles. Hallmarks of this entity include progressive cognitive decline, myoclonia, a generalized periodic pattern on EEG and...
13.
Treves S, Vukcevic M, Jeannet P, Levano S, Girard T, Urwyler A, et al.
Hum Mol Genet
. 2010 Nov;
20(3):589-600.
PMID: 21088110
Prolonged depolarization of skeletal muscle cells induces entry of extracellular calcium into muscle cells, an event referred to as excitation-coupled calcium entry. Skeletal muscle excitation-coupled calcium entry relies on the...
14.
Brinas L, Richard P, Quijano-Roy S, Gartioux C, Ledeuil C, Lacene E, et al.
Ann Neurol
. 2010 Oct;
68(4):511-20.
PMID: 20976770
Objective: Mutations in the genes encoding the extracellular matrix protein collagen VI (ColVI) cause a spectrum of disorders with variable inheritance including Ullrich congenital muscular dystrophy, Bethlem myopathy, and intermediate...
15.
Newman C, Jacquemont S, Theumann N, Jeannet P
Acta Paediatr
. 2010 Oct;
100(3):464-6.
PMID: 20955206
Unlabelled: A 5-year-old boy was referred to our neurology clinic for suspected myopathy. His parents reported normal upper extremity strength and no limitation in daily activities; however, he was unable...
16.
Jeannet P, Aminian K, Bloetzer C, Najafi B, Paraschiv-Ionescu A
Eur J Paediatr Neurol
. 2010 Aug;
15(1):40-7.
PMID: 20719551
Multiple motor function and strength assessment tools exist for the evaluation of neuromuscular diseases, but most do not directly assess functional ability in the patients' daily physical activity in their...
17.
Grunt S, Wingeier K, Wehrli E, Boltshauser E, Capone A, Fluss J, et al.
Dev Med Child Neurol
. 2010 Jun;
52(12):1145-50.
PMID: 20573178
Unlabelled: AIMo describe the characteristics of paediatric cerebral sinus venous thrombosis (CSVT) in Switzerland. Method: data on clinical features, neuroimaging, risk factors, and treatment were collected for all children in...
18.
Buerki S, Roellin K, Remonda L, Mercati D, Jeannet P, Keller E, et al.
Dev Med Child Neurol
. 2010 May;
52(11):1033-7.
PMID: 20477838
Aim: The aim of this study was to describe neuroimaging patterns associated with arterial ischaemic stroke (AIS) in childhood and to differentiate them according to stroke aetiology. Method: Clinical and...
19.
Ballhausen D, Guerry F, Hahn D, Schaller A, Nuoffer J, Bonafe L, et al.
J Inherit Metab Dis
. 2010 May;
33 Suppl 3:S219-26.
PMID: 20458543
Mitochondrial tRNA(Leu(UUR)) mutation m.3302A > G is associated with respiratory chain complex I deficiency and has been described as a rare cause of mostly adult-onset slowly progressive myopathy. Five families...
20.
Newman C, Holenweg-Gross C, Vuillerot C, Jeannet P, Roulet-Perez E
Arch Dis Child
. 2010 May;
95(5):387-90.
PMID: 20457703
Objective: To determine the frequency of recent skin injuries in children with neuromotor disabilities and its association with disability. Design: Cross-sectional study of 168 children with neuromotor disabilities aged 2-16...