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Results: 26-40/40
Authors:
Milea, D
Cassoux, N
Lehoang, P
Gerber, S
Marsault, C
Piette, JC
Amoura, Z
Kieffer, E
Citation: D. Milea et al., Neovascular glaucoma after bypass surgery in Takayasu's disease, EYE, 13, 1999, pp. 786-789
Authors:
Gerber, S
Basham, A
Citation: S. Gerber et A. Basham, Responsive therapy and motivational interviewing: Postmodernist paradigms, J COUNS DEV, 77(4), 1999, pp. 418-422
Authors:
Oppenheim, C
Stanescu, R
Dormont, D
Gerber, S
Marro, B
Sahel, M
Samson, Y
Marsault, C
Citation: C. Oppenheim et al., Diffusion MRI and brain ischemia : when is ADC mapping needed?, J NEURORAD, 26(4), 1999, pp. 242-248
Authors:
Souied, EH
Ducroq, D
Rozet, JM
Gerber, S
Perrault, I
Sterkers, M
Benhamou, N
Munnich, A
Coscas, G
Soubrane, G
Kaplan, J
Citation: Eh. Souied et al., A novel ABCR nonsense mutation responsible for late-onset fundus flavimaculatus, INV OPHTH V, 40(11), 1999, pp. 2740-2744
Authors:
Krautscheid, H
Gerber, S
Citation: H. Krautscheid et S. Gerber, The SCN- ion as an ambidentate ligand - Synthesis and crystal structures of (Bu4N)(4)[Ag2Fe2(SCN)(12)] and (Et4N)(2) (1)(infinity)[Ag2Fe(SCN)(6)], Z ANORG A C, 625(12), 1999, pp. 2041-2044
Authors:
Rozet, JM
Gerber, S
Ghazi, I
Perrault, I
Ducroq, D
Souied, E
Cabot, A
Dufier, JL
Munnich, A
Kaplan, J
Citation: Jm. Rozet et al., Mutations of the retinal specific ATP binding transporter gene (ABCR) in asingle family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evidence of clinical heterogeneity at this locus, J MED GENET, 36(6), 1999, pp. 447-451
Authors:
Berguer, R
Gerber, S
Kilpatrick, G
Remler, M
Beckley, D
Citation: R. Berguer et al., A comparison of forearm and thumb muscle electromyographic responses to the use of laparoscopic instruments with either a finger grasp or a palm grasp, ERGONOMICS, 42(12), 1999, pp. 1634-1645
Authors:
Wechsler, B
Gerber, S
Vidailhet, M
Dormont, D
Citation: B. Wechsler et al., Neurological manifestations of Behcet's disease., ANN MED IN, 150(7), 1999, pp. 555-561
Authors:
Souied, EH
Ducroq, D
Gerber, S
Ghazi, I
Rozet, JM
Perrault, I
Munnich, A
Dufier, JL
Coscas, C
Soubrane, G
Kaplan, J
Citation: Eh. Souied et al., Age-related macular degeneration in grandparents of patients with Stargardt disease: Genetic study, AM J OPHTH, 128(2), 1999, pp. 173-178
Authors:
Cabot, A
Rozet, JM
Gerber, S
Perrault, I
Ducroq, D
Smahi, A
Souied, E
Munnich, A
Kaplan, J
Citation: A. Cabot et al., A gene for X-linked idiopathic congenital nystagmus (NYS1) maps to chromosome Xp11.4-p11.3, AM J HU GEN, 64(4), 1999, pp. 1141-1146
Authors:
Perrault, I
Rozet, JM
Ghazi, I
Leowski, C
Bonnemaison, M
Gerber, S
Ducroq, D
Cabot, A
Souied, E
Dufier, JL
Munnich, A
Kaplan, J
Citation: I. Perrault et al., Different functional outcome of RetGC1 and RPE65 gene mutations in Leber congenital amaurosis, AM J HU GEN, 64(4), 1999, pp. 1225-1228
Authors:
Genolet, PM
Gerber, S
De Grandi, P
Friberg, B
Ahlgren, M
Citation: Pm. Genolet et al., Endometrial ablation for dysfunctional uterine bleeding in the perimenopause, clinical results of a multicentre trial with the Cavaterm (TM) thermal balloon, 9TH INTERNATIONAL MENOPAUSE SOCIETY WORLD CONGRESS ON THE MENOPAUSE, 1999, pp. 315-320
Authors:
Souied, EH
Rozet, JM
Gerber, S
Dufier, JL
Soubrane, G
Coscas, G
Munnich, A
Kaplan, J
Citation: Eh. Souied et al., Two novel missense mutations in the peripherin/RDS gene in two unrelated French patients with autosomal dominant retinitis pigmentosa, EUR J OPTHA, 8(2), 1998, pp. 98-101
Authors:
Kaplan, J
Rozet, JM
Gerber, S
Ducroq, D
Souied, E
Perrault, I
Munnich, A
Citation: J. Kaplan et al., Inherited macular dystrophies, M S-MED SCI, 14(12), 1998, pp. 1329-1336
Authors:
Wirz, C
Gerber, S
Genolet, PM
De Grandi, P
Citation: C. Wirz et al., Clinical results with the Cavaterm (TM) thermal balloon endometrial ablation technique for the treatment of menorrhagia, 7TH CONGRESS OF THE EUROPEAN SOCIETY FOR GYNAECOLOGICAL ENDOSCOPY, 1998, pp. 21-25