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Hepatitis E virus and neurologic disorders
N Kamar, RP Bendall, JM Peron, P Cintas, L Prudhomme, JM Mansuy, ...
Emerging infectious diseases 17 (2), 173, 2011
3782011
Hepatitis E virus and neurological injury
HR Dalton, N Kamar, JJJ Van Eijk, BN Mclean, P Cintas, RP Bendall, ...
Nature Reviews Neurology 12 (2), 77, 2016
2362016
Causes of death amongst French patients with amyotrophic lateral sclerosis: a prospective study
J Gil, B Funalot, A Verschueren, V Danel‐Brunaud, W Camu, ...
European journal of neurology 15 (11), 1245-1251, 2008
1962008
Hepatitis E virus‐induced neurological symptoms in a kidney‐transplant patient with chronic hepatitis
N Kamar, J Izopet, P Cintas, C Garrouste, E Uro‐Coste, O Cointault, ...
American Journal of Transplantation 10 (5), 1321-1324, 2010
1802010
Development and validation of a new risk prediction score for life-threatening ventricular tachyarrhythmias in laminopathies
K Wahbi, R Ben Yaou, E Gandjbakhch, F Anselme, T Gossios, ...
Circulation 140 (4), 293-302, 2019
1612019
Gender as a modifying factor influencing myotonic dystrophy type 1 phenotype severity and mortality: a nationwide multiple databases cross-sectional observational study
C Dogan, M De Antonio, D Hamroun, H Varet, M Fabbro, F Rougier, ...
PloS one 11 (2), e0148264, 2016
1572016
High rate of recanalization of middle cerebral artery occlusion during 2-MHz transcranial color-coded Doppler continuous monitoring without thrombolytic drug
P Cintas, AP Le Traon, V Larrue
Stroke 33 (2), 626-628, 2002
1352002
Enhancement of enzymatic fibrinolysis with 2‐MHz ultrasound and microbubbles
P Cintas, F Nguyen, B Boneu, V Larrue
Journal of Thrombosis and Haemostasis 2 (7), 1163-1166, 2004
1312004
Mutation Update and Genotype–Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies
M Marttila, VL Lehtokari, S Marston, TA Nyman, C Barnerias, AH Beggs, ...
Human mutation 35 (7), 779-790, 2014
1132014
Hepatitis E virus infection and acute non-traumatic neurological injury: a prospective multicentre study
HR Dalton, JJJ van Eijk, P Cintas, RG Madden, C Jones, GW Webb, ...
Journal of hepatology 67 (5), 925-932, 2017
1002017
Guidance for the care of neuromuscular patients during the COVID-19 pandemic outbreak from the French Rare Health Care for Neuromuscular Diseases Network
G Solé, E Salort-Campana, Y Pereon, T Stojkovic, K Wahbi, P Cintas, ...
Revue neurologique 176 (6), 507-515, 2020
952020
Atrial fibrillation and subtype of atrial fibrillation in cardiac amyloidosis: clinical and echocardiographic features, impact on mortality
K Sanchis, E Cariou, M Colombat, D Ribes, A Huart, P Cintas, P Fournier, ...
Amyloid 26 (3), 128-138, 2019
762019
Acute hepatitis E in French patients and neurological manifestations
F Abravanel, J Pique, E Couturier, F Nicot, C Dimeglio, S Lhomme, ...
Journal of Infection 77 (3), 220-226, 2018
752018
Neurologic disorders in immunocompetent patients with autochthonous acute hepatitis E
HB Perrin, P Cintas, F Abravanel, R Gerolami, L d'Alteroche, JN Raynal, ...
Emerging Infectious Diseases 21 (11), 1928, 2015
742015
Increased exposure to statins in patients developing chronic muscle diseases: a 2-year retrospective study
L Sailler, C Pereira, A Bagheri, M Lapeyre-Mestre, JL Montastruc, P Arlet, ...
Annals of the rheumatic diseases 67 (5), 614-619, 2008
562008
Bent spine syndrome (camptocormia): a retrospective study of 63 patients
M Laroche, P Cintas
Joint Bone Spine 77 (6), 593-596, 2010
552010
Impact of coronavirus disease 2019 in a French cohort of myasthenia gravis
G Solé, S Mathis, D Friedman, E Salort-Campana, C Tard, F Bouhour, ...
Neurology 96 (16), e2109-e2120, 2021
532021
Which method for diagnosing small fiber neuropathy?
V Fabry, A Gerdelat, B Acket, P Cintas, V Rousseau, E Uro-Coste, ...
Frontiers in Neurology 11, 342, 2020
512020
Adult Niemann-Pick disease type C in France: clinical phenotypes and long-term miglustat treatment effect
Y Nadjar, AL Hütter-Moncada, P Latour, X Ayrignac, E Kaphan, ...
Orphanet journal of rare diseases 13, 1-12, 2018
492018
Dehydroepiandrosterone for myotonic dystrophy type 1
I Pénisson-Besnier, M Devillers, R Porcher, D Orlikowski, V Doppler, ...
Neurology 71 (6), 407-412, 2008
382008
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