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Results:
1-15
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Results: 15
Authors:
Biswas, S
Munier, FL
Yardley, J
Hart-Holden, N
Perveen, R
Cousin, P
Sutphin, JE
Noble, B
Batterbury, M
Kielty, C
Hackett, A
Bonshek, R
Ridgway, A
McLeod, D
Sheffield, VC
Stone, EM
Schorderet, DF
Black, GCM
Citation: S. Biswas et al., Missense mutations in COL8A2, the gene encoding the alpha 2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy, HUM MOL GEN, 10(21), 2001, pp. 2415-2423
Authors:
Chaubert, P
Burri, N
Cousin, P
Shaw, P
Citation: P. Chaubert et al., A novel highly informative polyA microsatellite on the telomeric side of the INK4a/ARF locus, MOL CELL PR, 15(3), 2001, pp. 183-185
Authors:
Zankl, A
Addor, MC
Cousin, P
Gaide, AC
Gudinchet, F
Schorderet, DF
Citation: A. Zankl et al., Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene, EUR J PED, 160(5), 2001, pp. 296-299
Authors:
Cousin, P
Billotte, J
Chaubert, P
Shaw, P
Citation: P. Cousin et al., Physical map of 17p13 and the Genes Adjacent to p53, GENOMICS, 63(1), 2000, pp. 60-68
Authors:
Cornu, C
Mercier, C
Ffrench, P
Bully, C
Pugeat, M
Cousin, P
Riou, JP
Bajart, L
Orgiazzi, J
Pommet-Nicot, C
Darsy, P
Boissel, JP
Berthezene, F
Citation: C. Cornu et al., Postmenopause hormone treatment in women with NIDDM or impaired glucose tolerance: the MEDIA randomized clinical trial, MATURITAS, 37(2), 2000, pp. 95-104
Authors:
Pugeat, M
Cousin, P
Baret, C
Lejeune, H
Forest, MG
Citation: M. Pugeat et al., Sex hormone-binding globulin during puberty in normal and hyperandrogenic girls, J PED END M, 13, 2000, pp. 1277-1279
Authors:
Zankl, A
Addor, MC
Gaide, AC
Thonney, F
Cousin, P
Schorderet, DF
Gudinchet, F
Nenadov-Beck, M
Citation: A. Zankl et al., Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome, AM J MED G, 95(5), 2000, pp. 510-512
Authors:
Emptoz-Bonneton, A
Cousin, P
Seguchi, K
Avvakumov, GV
Bully, C
Hammond, GL
Pugeat, M
Citation: A. Emptoz-bonneton et al., Novel human corticosteroid-binding globulin variant with low cortisol-binding affinity, J CLIN END, 85(1), 2000, pp. 361-367
Authors:
Pugeat, M
Bendridi, N
Cousin, P
Citation: M. Pugeat et al., Phytoestrogens: modulators of estrogen receptors: food additive or alternative therapy?, ANN ENDOCR, 61(5), 2000, pp. 477-477
Authors:
Macari, F
Landau, M
Cousin, P
Mevorah, B
Brenner, S
Panizzon, R
Schorderet, DF
Hohl, D
Huber, M
Citation: F. Macari et al., Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis, AM J HU GEN, 67(5), 2000, pp. 1296-1301
Authors:
Stone, EM
Lotery, AJ
Munier, FL
Heon, E
Piguet, B
Guymer, RH
Vandenburgh, K
Cousin, P
Nishimura, D
Swiderski, RE
Silvestri, G
Mackey, DA
Hageman, GS
Bird, AC
Sheffield, VC
Schorderet, DF
Citation: Em. Stone et al., A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy, NAT GENET, 22(2), 1999, pp. 199-202
Authors:
Cousin, P
Dechaud, H
Grenot, C
Lejeune, H
Hammond, GL
Pugeat, M
Citation: P. Cousin et al., Influence of glycosylation on the clearance of recombinant human sex hormone-binding globulin from rabbit blood, J STEROID B, 70(4-6), 1999, pp. 115-121
Authors:
Parrat, E
Brousse, D
Cousin, P
L'Herron, F
Touameur, S
Charpentier, D
David, T
Citation: E. Parrat et al., Association of Fuchs' uveitic syndrome and toxoplasmosis: a case report, J FR OPHTAL, 22(10), 1999, pp. 1067-1071
Authors:
Cousin, P
Fourmaux, E
Renaud-Rougier, MB
Mercie, M
Pincemin, D
Le Rebeller, MJ
Citation: P. Cousin et al., Bilateral anterior ischemic optic neuropathy caused by optic nerve head drusen: a case report, J FR OPHTAL, 22(1), 1999, pp. 79-83
Authors:
Cousin, P
Anselme, G
Courtois, G
Mesnard, D
Citation: P. Cousin et al., Efficient monohydroxyarylation (or alkylation) and symmetrical bis-hydroxyarylation (or alkylation) of 2,5-dimethyl-1,3,4-thiadiazole, SYN COMMUN, 29(1), 1999, pp. 145-156
Risultati:
1-15
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