AAAAAA
Results:
1-13
|
Results: 13
Authors:
Marteau, P
Verkarre, V
Andre, C
Brousse, N
Cellier, C
Citation: P. Marteau et al., Comments on case reports: Diarrhea with vitamin B12 deficiency, GASTRO CL B, 25(5), 2001, pp. 495-497
Authors:
Camara-Clayette, V
Rahuel, C
Lopez, C
Hattab, C
Verkarre, V
Bertrand, O
Cartron, JP
Citation: V. Camara-clayette et al., Transcriptional regulation of the KEL gene and Kell protein expression in erythroid and non-erythroid cells, BIOCHEM J, 356, 2001, pp. 171-180
Authors:
de Serre, NPM
Verkarre, V
Cellier, C
Cerf-Bensussan, N
Schmitz, J
Brousse, N
Citation: Npm. De Serre et al., Etiological diagnosis of villous atrophy, ANN PATHOL, 21(4), 2001, pp. 319-333
Authors:
Fournet, JC
Mayaud, C
de Lonlay, P
Gross-Morand, MS
Verkarre, V
Castanet, M
Devillers, M
Rahier, J
Brunelle, F
Robert, JJ
Nihoul-Fekete, C
Saudubray, JM
Junien, C
Citation: Jc. Fournet et al., Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism - Association with a reduction to hamozygosity of a mutation in ABCC8 or KCNJ11, AM J PATH, 158(6), 2001, pp. 2177-2184
Authors:
Gandemer, V
Verkarre, V
Quartier, P
Brousse, N
Blanche, S
Citation: V. Gandemer et al., Lymphoma in HIV 1-infected children., ARCH PED, 7(7), 2000, pp. 738-744
Authors:
De Serre, NPM
Verkarre, V
Cellier, C
Cerf-Bensussan, N
Schmitz, J
Brousse, N
Citation: Npm. De Serre et al., Etiological diagnosis of villous atrophy, GASTRO CL B, 24(4), 2000, pp. 436-446
Authors:
de Serre, NPM
Cellier, C
Jabri, B
Delabesse, E
Verkarre, V
Roche, B
Lavergne, A
Briere, J
Mauvieux, L
Leborgne, M
Barbier, JP
Modigliani, R
Matuchansky, C
Macintyre, E
Cerf-Bensussan, N
Brousse, N
Citation: Npm. De Serre et al., Distinction between coeliac disease and refractory sprue: a simple immunohistochemical method, HISTOPATHOL, 37(1), 2000, pp. 70-77
Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism
Authors:
Fournet, JC
Mayaud, C
de Lonlaya, P
Verkarre, V
Rahier, J
Brunelle, F
Robert, JJ
Nihoul-Fekete, C
Saudubray, JM
Junien, C
Citation: Jc. Fournet et al., Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism, HORMONE RES, 53, 2000, pp. 2-6
Authors:
Verkarre, V
de Serre, NPM
Vazeux, R
Teillac-Hamel, D
Chretien-Marquet, B
Le Bihan, C
Leborgne, M
Fraitag, S
Brousse, N
Citation: V. Verkarre et al., ICAM-3 and E-selectin endothelial cell expression differentiate two phasesof angiogenesis in infantile hemangiomas, J CUT PATH, 26(1), 1999, pp. 17-24
Authors:
Cellier, C
Cuillerier, E
de Serre, NPM
Marteau, P
Verkarre, V
Briere, J
Brousse, N
Barbier, JP
Schmitz, J
Landi, B
Citation: C. Cellier et al., Push enteroscopy in celiac sprue and refractory sprue, GASTROIN EN, 50(5), 1999, pp. 613-617
Authors:
Brousse, N
Verkarre, V
de Serre, NPM
Cellier, C
Cerf-Bensussan, N
Delabesse, E
Macintyre, E
Citation: N. Brousse et al., Is complicated celiac disease or refractory sprue an intestinal intra-epithelial cryptic T-cell lymphoma?, BLOOD, 93(9), 1999, pp. 3154-3155
Authors:
Fournet, JC
Verkarre, V
de Lonlay, P
Rahier, J
Brunelle, F
Robert, JJ
Nihoul-Fekete, C
Saudubray, JM
Junien, C
Citation: Jc. Fournet et al., Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia, ANN ENDOCR, 59(6), 1998, pp. 485-491
Authors:
Fournet, JC
De Lonlay, P
Verkarre, V
Gross-Morand, MS
Rahier, J
Brunelle, F
Roberts, JJ
Nihoul-Fekete, C
Saudubray, JM
Junien, C
Citation: Jc. Fournet et al., Endocrine tumors - Somatic recessive diseases, EUROCANCER 98, 1998, pp. 117-118
Risultati:
1-13
|