Search Results - "Vanlander, A"

Pure Laparoscopic Full‐Left Living Donor Hepatectomy for Calculated Small‐for‐Size LDLT in Adults: Proof of Concept by Troisi, R. I., Wojcicki, M., Tomassini, F., Houtmeyers, P., Vanlander, A., Berrevoet, F., Smeets, P., Van Vlierberghe, H., Rogiers, X.

“…Adult‐to‐adult living donor liver transplantation (A2ALDLT) is an accepted mode of treatment for end‐stage liver disease. Right‐lobe grafts have usually been…”
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Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre, phase 3 trial by Mercuri, Eugenio, Muntoni, Francesco, Baranello, Giovanni, Masson, Riccardo, Boespflug-Tanguy, Odile, Bruno, Claudio, Corti, Stefania, Daron, Aurore, Deconinck, Nicolas, Servais, Laurent, Straub, Volker, Ouyang, Haojun, Chand, Deepa, Tauscher-Wisniewski, Sitra, Mendonca, Nuno, Lavrov, Arseniy, Seferian, A., De Lucia, S., Tachibana, S., Jollet, A., Mouffak, S., Pedemonte, M., Brolatti, N., Morando, S., Vanlander, A., De Vos, E., Tahon, V., Govoni, A., Magri, F., Comi, G., Foa, M., Parente, V., Buscemi, L., Dal Farra, F., Schneider, O., Jonas, A., Defeldre, A.C., Pagliano, E., Zanin, R., Arnoldi, M.T., Schembri, V., Del Sole, M., Mandelli, A., Pera, M.C., Antonaci, L., Coratti, G., de Sanctis, R., Pane, M., Scoto, M., Groves, K., Edel, L., Abel, F., Van Ruiten, H., Lofra, R.M., Thompson, E.

“…Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease caused by biallelic loss of the survival motor neuron 1 (SMN1) gene, resulting in…”
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Clinical and genetic aspects of defects in the mitochondrial iron–sulfur cluster synthesis pathway by Vanlander, A. V., Van Coster, R.

“…Iron–sulfur clusters are evolutionarily conserved biological structures which play an important role as cofactor for multiple enzymes in eukaryotic cells. The…”
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EHS clinical guidelines on the management of the abdominal wall in the context of the open or burst abdomen by López-Cano, M., García-Alamino, J. M., Antoniou, S. A., Bennet, D., Dietz, U. A., Ferreira, F., Fortelny, R. H., Hernandez-Granados, P., Miserez, M., Montgomery, A., Morales-Conde, S., Muysoms, F., Pereira, J. A., Schwab, R., Slater, N., Vanlander, A., Van Ramshorst, G. H., Berrevoet, F.

“…Purpose To provide guidelines for all surgical specialists who deal with the open abdomen (OA) or the burst abdomen (BA) in adult patients both on the methods…”
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Correction to: Clinical and genetic aspects of defects in the mitochondrial iron–sulfur cluster synthesis pathway by Vanlander, A. V., Van Coster, R.

“…The article “Clinical and genetic aspects of defects in the mitochondrial iron–sulfur cluster synthesis pathway”, written by A. V. Vanlander, R. Van Coster was…”
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Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humans by Vandecasteele, S.J., Seneca, S., Smet, J., Reynders, M., De Ceulaer, J., Vanlander, A.V., van Coster, R.

“…A 65-year-old patient developed an unexplained and ultimately lethal metabolic acidosis under prolonged treatment with tigecycline. Tigecycline is known to…”
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Infected large pore meshes may be salvaged by topical negative pressure therapy by Berrevoet, F., Vanlander, A., Sainz-Barriga, M., Rogiers, X., Troisi, R.

“…Purpose To evaluate the efficacy of negative pressure therapy for superficial and deep mesh infections after ventral and incisional hernia repair by a…”
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Added Value of 3D-vision During Biotissue Robotic Pancreatoduodenectomy Anastomoses (LAEBOT-3D2D): a Randomized Controlled Cross-Over Trial by Zwart, M., Jones, L., Balduzzi, B., Takagi, K., Vanlander, A., Den Boezem P., Van, Daams, F., Rosman, C., Lips, D., Moser, A., Hogg, M., Busch, O., Stommel, M., Besselink, M.

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Pretransplant glycomic analysis of perfusate is predictive of primary non function after liver transplantation by Verhelst, X, Geerts, A, Vanderschaeghe, D, Rogiers, X, Vanlander, A, Berrevoet, F, Callewaert, N, Troisi, R.I, Van Vlierberghe, H

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A glycomic serum marker analysed at one week after liver transplantation is an independent predictor of graft loss during the first year after liver transplantation by Verhelst, X, Geerts, A, Rogiers, X, Vanlander, A, Berrevoet, F, Callewaert, N, Troisi, R.I, Van Vlierberghe, H

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Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome by VANLANDER, A. V., JORENS, P. G., SMET, J., DE PAEPE, B., VERBRUGGHE, W., VAN DEN EYNDEN, G. G., MEIRE, F., PAUWELS, P., VAN DER AA, N., SENECA, S., LISSENS, W., OKUN, J. G., VAN COSTER, R.

“…Propofol is an anesthetic agent widely used for induction and maintenance of anesthesia, and sedation in children. Although generally considered as reliable…”
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Performance with robotic surgery versus 3D- and 2D-laparoscopy during pancreatic and biliary anastomoses in a biotissue model: Pooled analysis of two randomized trials by Zwart, M., Jones, L., Fuente, I., Balduzzi, A., Takagi, K., Novak, S., Stibbe, L., de Rooij, T., van Hilst, J., van Rijssen, B., van Dieren, S., Vanlander, A., van den Boezem, P., Daams, F., Mieog, S., Bonsing, B., Rosman, C., Festen, S., Luyer, M., Lips, D., Moser, A., Busch, O., Hilal, M. Abu, Hogg, M., Stommel, M., Besselink, M.

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Discussion about PG versus PJ in (PP)PD for pancreatic adenocarcinoma is nonsense, standardization through volume is the key by Berrevoet, F, Vanlander, A, Verlinden, J, Laurent, S

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META Score: An International Consensus Scoring System on Mesh-Tissue Adhesions by van den Hil, L. C. L., Mommers, E. H. H., Bosmans, J. W. A. M., Morales-Conde, S., Gómez-Gil, V., LeBlanc, K., Vanlander, A., Reynvoet, E., Berrevoet, F., Gruber-Blum, S., Altinli, E., Deeken, C. R., Fortelny, R. H., Greve, J. W., Chiers, K., Kaufmann, R., Lange, J. F., Klinge, U., Miserez, M., Petter-Puchner, A. H., Schreinemacher, M. H. F., Bouvy, N. D.

“…Background Currently, the lack of consensus on postoperative mesh-tissue adhesion scoring leads to incomparable scientific results. The aim of this study was…”
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P0075 : Health-related quality of life is improved after liver transplantation and is related to disease acceptance, helplessness and perceived disease benefits by Develtere, W, Onghena, L, Rogiers, X, Troisi, R.I, Berrevoet, F, Vanlander, A, Geerts, A, Van Vlierberghe, H, Verhelst, X, Poppe, C

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Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2 by Vantroys, E, Smet, J, Vanlander, A, De Paepe, B, Vergult, S, Sante, T, Menten, B, Van Coster, R

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Open preperitoneal mesh repair of inguinal hernias using a mesh with nitinol memory frame by Berrevoet, F., Vanlander, A., Bontinck, J., Troisi, R. I.

“…Purpose To prospectively evaluate the use of a continuous Nitinol containing memory frame patch during a TIPP-technique in the open repair of inguinal and…”
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Riboflavin-responsive ACAD9 mutation as cause of familial hypertrophic cardiomyopathy by Van Coster, R, Stepman, H, Vanlander, A, Smet, J, Seneca, S, Vantroys, E, De Meirleir, L

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Pathogenic mutations in TMEM126B, a recently discovered complex I assembly factor, identified in four siblings from two Belgian families by Van Coster, R, Smet, J, De Paepe, B, Vanlander, A, Vantroys, E, Alston, C, Compton, A, Torburn, D, Seneca, S, Taylor, R

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G.P.215 by Deconinck, N, De Paepe, B, Symoens, S, Vanlander, A, Gartioux, C, Allamand, V, Smet, J, Devreese, B, Van Coster, R

“…Ullrich congenital muscular dystrophy (UCMD) is a severe congenital dystrophy caused by collagen VI (COL VI) mutations and resulting in absent or aberrant…”
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