检索结果 - Slama, A

Two year maintenance treatment of duodenal ulcer disease with ranitidine 150 mg: a prospective multicentre randomised study. GEMUD (Groupe d'Etude de la Maladie Ulcéreuse Duodénale... 由 Ruszniewski, P, Slama, A, Pappo, M, Mignon, M

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Amphotericin B® treatment causes QT prolongation in lung transplant-patients 由 Tudor, B-A, Slama, A, Roth, GA, Krenn, C-G

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Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts. 由 Pande, S V, Brivet, M, Slama, A, Demaugre, F, Aufrant, C, Saudubray, J M

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ATP-modulated K+ channels sensitive to antidiabetic sulfonylureas are present in adenohypophysis and are involved in growth hormone release. 由 Bernardi, H, De Weille, J R, Epelbaum, J, Mourre, C, Amoroso, S, Slama, A, Fosset, M, Lazdunski, M

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Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome 由 Benit, P, Slama, A, Cartault, F, Giurgea, I, Chretien, D, Lebon, S, Marsac, C, Munnich, A, Rotig, A, Rustin, P

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The First Experience of Ex-Vivo Lung Perfusion (EVLP) in Iran: An Effective Method to Increase Suitable Lung for Transplantation 由 Shafaghi, S., Najafizadeh, K., Sheikhy, K., Ansari Aval, Z., Farzanegan, B., Mafhoomi, Y., Faghih Abdollahi, Z., Emami, H., Mortaz, E., Porabdollah, M., Jahangiri Fard, A., Nikobayan Safaei, M., Slama, A., Aigner, C., Hosseini-Baharanchi, F. S., Abbasi Dezfuli, A.

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Natural disease course and genotype-phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases 由 Koene, S., Rodenburg, R. J., van der Knaap, M. S., Willemsen, M. A. A. P., Sperl, W., Laugel, V., Ostergaard, E., Tarnopolsky, M., Martin, M. A., Nesbitt, V., Fletcher, J., Edvardson, S., Procaccio, V., Slama, A., van den Heuvel, L. P. W. J., Smeitink, J. A. M.

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