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Results: 1-25/34
Authors:
Dubourg, O
Tardieu, S
Birouk, N
Gouider, R
Leger, JM
Maisonobe, T
Brice, A
Bouche, P
LeGuern, E
Citation: O. Dubourg et al., The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity, NEUROMUSC D, 11(5), 2001, pp. 458-463
Authors:
Qanadli, SD
Mesurolle, B
Aegerter, P
Joseph, T
Oliva, VL
Guertin, MC
Dubourg, O
Fauchet, M
Goeau-Brissonniere, OA
Lacombe, P
Citation: Sd. Qanadli et al., Volumetric quantification of coronary artery calcifications using dual-slice spiral CT scanner: Improved reproducibility of measurements with 180 degrees linear interpolation algorithm, J COMPUT AS, 25(2), 2001, pp. 278-286
Authors:
Qanadli, SD
El Hajjam, M
Vieillard-Baron, A
Joseph, T
Mesurolle, B
Oliva, VL
Barre, O
Bruckert, F
Dubourg, O
Lacombe, P
Citation: Sd. Qanadli et al., New CT index to quantify arterial obstruction in pulmonary embolism: Comparison with angiographic index and echocardiography, AM J ROENTG, 176(6), 2001, pp. 1415-1420
Authors:
Vieillard-Baron, A
Page, B
Augarde, R
Prin, S
Qanadli, S
Beauchet, A
Dubourg, O
Jardin, F
Citation: A. Vieillard-baron et al., Acute cor pulmonale in massive pulmonary embolism: incidence, echocardiographic pattern, clinical implications and recovery rate, INTEN CAR M, 27(9), 2001, pp. 1481-1486
Authors:
Pingault, V
Bondurand, N
Le Caignec, C
Tardieu, S
Lemort, N
Dubourg, O
Le Guern, E
Goossens, M
Boespflug-Tanguy, O
Citation: V. Pingault et al., The SOX10 transcription factor: evaluation as a candidate gene for centraland peripheral hereditary myelin disorders, J NEUROL, 248(6), 2001, pp. 496-499
Authors:
Lacombe, P
Qanadli, SD
Heautot, JF
Guichoux, F
Mignon, F
Leclercq, C
Dubourg, O
Changnon, S
Citation: P. Lacombe et al., Coronary steal syndrome by systemic hypervascularization of the lung via amammary - left anterior descending artery bypass. Treatment by embolization, J RADIOLOG, 82(2), 2001, pp. 168-170
Authors:
Dubourg, O
Tardieu, S
Birouk, N
Gouider, R
Leger, JM
Maisonobe, T
Brice, A
Bouche, P
LeGuern, E
Citation: O. Dubourg et al., Clinical, electrophysiological and molecular genetic characteristics of 93patients with X-linked Charcot-Marie-Tooth disease, BRAIN, 124, 2001, pp. 1958-1967
Authors:
Dubourg, O
Mouton, P
Brice, A
LeGuern, E
Bouche, P
Citation: O. Dubourg et al., Guidelines for diagnosis of hereditary neuropathy with liability to pressure palsies, NEUROMUSC D, 10(3), 2000, pp. 206-208
Authors:
Gosse, P
Sheridan, DJ
Zannad, F
Dubourg, O
Gueret, P
Karpov, Y
de Leeuw, PW
Palma-Gamiz, JL
Pessina, A
Motz, W
Degaute, JP
Chastang, C
Citation: P. Gosse et al., Regression of left ventricular hypertrophy in hypertensive patients treated with indapamide SR 1.5 mg versus enalapril 20 mg: the LIVE study, J HYPERTENS, 18(10), 2000, pp. 1465-1475
Authors:
Izzillo, R
Qanadli, SD
Staroz, F
Dubourg, O
Laborde, F
Raguin, G
Lacombe, P
Citation: R. Izzillo et al., Leiomyosarcoma of the superior vena cava: diagnosis by endovascular biopsy, J RADIOLOG, 81(6), 2000, pp. 632-635
Authors:
El Hajjam, M
Gevenois, PA
Qanadli, SD
Dubourg, O
Bourdarias, JP
Lacombe, P
Citation: M. El Hajjam et al., Diagnosis of saphenous coronary graft aneurysm by spiral computed tomography, CARDIO IN R, 23(2), 2000, pp. 142-144
Authors:
Dubourg, O
Barhoumi, C
Azzedine, H
Birouk, N
Brice, A
Bouche, P
Leguern, E
Citation: O. Dubourg et al., Phenotypic and genetic study of a family with hereditary sensory neuropathy and prominent weakness, MUSCLE NERV, 23(10), 2000, pp. 1508-1514
Authors:
Bouche, P
Mouton, P
Gouider, R
Dubourg, O
Le Guern, E
Maisonobe, T
le Forestier, N
Citation: P. Bouche et al., Hereditary neuropathy by pressure hypersensitivity, REV NEUROL, 156(10), 2000, pp. 915-919
Authors:
Qanadli, SD
El Hajjam, M
Mesurolle, B
Barre, O
Bruckert, F
Joseph, T
Mignon, F
Vieillard-Baron, A
Dubourg, O
Lacombe, P
Citation: Sd. Qanadli et al., Pulmonary embolism detection: Prospective evaluation of dual-section helical CT versus selective pulmonary arteriography in 157 patients, RADIOLOGY, 217(2), 2000, pp. 447-455
Authors:
Richard, P
Charron, P
Leclercq, C
Ledeuil, C
Carrier, L
Dubourg, O
Desnos, M
Bouhour, JB
Schwartz, K
Daubert, JC
Komajda, M
Hainque, B
Citation: P. Richard et al., Homozygotes for a R869G mutation in the beta-myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathy, J MOL CEL C, 32(8), 2000, pp. 1575-1583
Authors:
Forissier, JF
Richard, P
Briault, S
Ledeuil, C
Dubourg, O
Charbonnier, B
Carrier, L
Moraine, C
Bonne, G
Komajda, M
Schwartz, K
Hainque, B
Citation: Jf. Forissier et al., First description of germline mosaicism in familial hypertrophic cardiomyopathy, J MED GENET, 37(2), 2000, pp. 132-134
Authors:
Vieillard-Baron, A
Loubieres, Y
Schmitt, JM
Page, B
Dubourg, O
Jardin, F
Citation: A. Vieillard-baron et al., Cyclic changes in right ventricular output impedance during mechanical ventilation, J APP PHYSL, 87(5), 1999, pp. 1644-1650
Authors:
Mangin, L
Charron, P
Tesson, F
Mallet, A
Dubourg, O
Desnos, M
Benaische, A
Gayet, C
Gibelin, P
Davy, JM
Bonnet, J
Sidi, D
Schwartz, K
Komajda, M
Citation: L. Mangin et al., Familial dilated cardiomyopathy: clinical features in French families, EUR J HE FA, 1(4), 1999, pp. 353-361
Authors:
Mesurolle, B
Qanadli, SD
Merad, M
Mignon, F
Lacombe, P
Dubourg, O
Citation: B. Mesurolle et al., Anomalous origin of the left coronary artery arising from the pulmonary trunk: report of an adult case with long-term follow-up after surgery, EUR RADIOL, 9(8), 1999, pp. 1570-1573
Authors:
Qanadli, SD
Mesurolle, B
Mignon, F
Barre, O
Bruckert, F
Dubourg, O
Chinet, T
Chagnon, S
Lacombe, P
Citation: Sd. Qanadli et al., Bronchial and pulmonary vaso-occlusions, REV MAL RES, 16(4BIS), 1999, pp. 719-729
Authors:
Lacombe, P
Qanadli, SD
Mignon, F
Sissakian, JF
Barre, O
El Hajjam, M
Dubourg, O
Citation: P. Lacombe et al., Stents in superior vena cava syndrome, REV MAL RES, 16, 1999, pp. S157-S161
Authors:
Qanadli, SD
Mesurolle, B
El Hajjam, M
Mignon, F
Guichoux, F
Dubourg, O
Chagnon, S
Lacombe, P
Citation: Sd. Qanadli et al., Helical Computed Tomography (CT) of the aorta and its branches, J RADIOLOG, 80(9), 1999, pp. 998-1008
Authors:
Lacombe, P
Qanadli, SD
Coggia, M
Mignon, F
Barre, O
Sissakian, JF
Bruckert, F
Chagnon, S
Dubourg, O
Citation: P. Lacombe et al., Positional occlusion of the descending scapular artery in a thoracic outlet syndrome with neurological symptoms, J RADIOLOG, 80(1), 1999, pp. 53-55
Authors:
Charron, P
Tesson, F
Poirier, O
Nicaud, V
Peuchmaurd, M
Tiret, L
Cambien, F
Amouyel, P
Dubourg, O
Bouhour, JB
Millaire, A
Juilliere, Y
Bareiss, P
Andre-Fouet, X
Pouillart, F
Arveiler, D
Ferrieres, J
Dorent, R
Roizes, G
Schwartz, K
Desnos, M
Komajda, M
Citation: P. Charron et al., Identification of a genetic risk factor for idiopathic dilated cardiomyopathy - Involvement of a polymorphism in the endothelin receptor type A gene, EUR HEART J, 20(21), 1999, pp. 1587-1591
Authors:
Mouton, P
Tardieu, S
Gouider, R
Birouk, N
Maisonabe, T
Dubourg, O
Brice, A
LeGuern, E
Bouche, P
Citation: P. Mouton et al., Spectrum of clinical and electrophysiologic features in HNPP patients withthe 17p11.2 deletion, NEUROLOGY, 52(7), 1999, pp. 1440-1446