Search Results - "Roijers, J."

VKORC1 and CYP2C9 Genotypes and Phenprocoumon Anticoagulation Status: Interaction Between both Genotypes Affects Dose Requirement by Schalekamp, T, Brassé, B P, Roijers, J F M, Meegen, E, Meer, F J M, Wijk, E M, Egberts, A C G, Boer, A

“…In a prospective follow‐up study of the effects of VKORC1 and CYP2C9 genotypes on the anticoagulation status of patients, we assessed the CYP2C9 and the VKORC1…”
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A Comparison of Health Status and Quality of Life in Patients with Intermittent Claudication by Roijers, J.P., van den Houten, M.M.L., Hopmans, C.J., Vriens, P.W.H.E., Willigendael, E.M., Lodder, P., de Vries, J., Teijink, J.A.W., van der Laan, L.

“…Patient reported outcome measures (PROMs) such as health status (HS) and quality of life (QOL) are frequently used interchangeably while they represent…”
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The Role of Delirium and Other Risk Factors on Mortality in Elderly Patients with Critical Limb Ischemia Undergoing Major Lower Limb Amputation by Roijers, J.P., Hopmans, C.J., Janssen, T.L., Mulder, P.G.H., Buimer, M.G., Ho, G.H., de Groot, H.G.W., Veen, E.J., van der Laan, L.

“…Delirium in patients with critical limb ischemia (CLI) is associated with increased mortality. The main goal of this study was to investigate the association…”
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Molecular test for the detection of tumor cells in blood and sentinel nodes of melanoma patients by Van der Velde-Zimmermann, D, Roijers, JF, Bouwens-Rombouts, A, De Weger, RA, De Graaf, PW, Tilanus, MG, Van den Tweel, JG

“…Lymph node metastasis dramatically decreases the 5-year survival of melanoma patients. The so-called sentinel node surgery offers a therapeutic approach to…”
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Adverse Cardiac Events and Mortality in Patients with Critical Limb Ischemia by Roijers, Joost J.P., Rakké, Bastiaan Y.S., Hopmans, Niels C.J., Buimer, Thijs M.G., Ho, Gwan G.H., de Groot, Hans H.G.W., Veen, Eelco E.J., Vos, Jeroen J., Mulder, Paul P.G.H., van der Laan, Lijckle L.

“…Both surgical and endovascular treatment in elderly patients with critical limb ischemia are associated with high mortality rates. Patients with critical limb…”
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Do Surgical Site Infections in Open Aortoiliac Surgery Differ Between Occlusive and Aneurysmal Arterial Disease? by Langenberg, J.C.M., Roijers, J., Kluytmans, J.A.J.W., de Goot, H.G.W., Ho, G.H., Veen, E.J.

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Hereditary tyrosinemia type 1 : novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene ; variability of the genotype-phenotype relationship by PLOOS VAN AMSTEL, J. K, BERGMAN, A. J. I. W, VAN BEURDEN, E. A. C. M, ROIJERS, J. F. M, PEELEN, T, VAN DEN BERG, I. E. T, POOL-THE, B. T, KVITTIGEN, E. A, BERGER, R

“…The complete fumarylacetoacetate hydrolase (FAH) genotype of probands of thirteen unrelated families with hereditary tyrosinemia type 1 (HT 1) was established…”
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The glucagonoma syndrome and necrolytic migratory erythema: a clinical review by VAN BEEK, André P, DE HAAS, Ellen R. M, VAN VLOTEN, Willem A, LIPS, Cees J. M, ROIJERS, Janine F. M, CANNINGA-VAN DIJK, Marijke R

“…The glucagonoma syndrome is a rare disease in which a typical skin disorder, necrolytic migratory erythema, is often one of the first presenting symptoms…”
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Criteria for mutation analysis in MEN 1-suspected patients: MEN 1 case-finding by Roijers, De Wit, Van Der Luijt, Ploos van Amstel, Höppener, Lips

“…Background Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal, dominantly inherited cancer syndrome, with tumours in various endocrine glands. In 1997…”
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VKORC1 and CYP2C9 genotypes and acenocoumarol anticoagulation status: Interaction between both genotypes affects overanticoagulation by SCHALEKAMP, T, BRASSE, B, ROIJERS, J, CHAHID, Y, VANGEESTDAALDEROP, J, DEVRIESGOLDSCHMEDING, H, VANWIJK, E, EGBERTS, A, DEBOER, A

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Pseudohypoparathyroidism type Ia. Albright hereditary osteodystrophy: a model for research on G protein-coupled receptors and genomic imprinting by Simon, A, Koppeschaar, H P, Roijers, J F, Höppener, J W, Lips, C J

“…Pseudohypoparathyroidism type Ia (PHP Ia) is a hereditary endocrine disorder, characterised by resistance to parathyroid hormone (PTH), causing disturbance of…”
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Internally shortened menin protein as a consequence of alternative RNA splicing due to a germline deletion in the multiple endocrine neoplasia type 1 gene by Roijers, J F, Apel, T, Neumann, H P, Arnim, U V, Lips, C J, Hoppener, J W

“…Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominantly inherited cancer syndrome (OMIM 131100), with tumours in several endocrine glands. In…”
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A Putative Human Zinc-Finger Gene (ZFPL1) on 11q13, Highly Conserved in the Mouse and Expressed in Exocrine Pancreas: The European Consortium on MEN 1 by Höppener, J.W.M., De Wit, M.J., Simarro-Doorten, A.Y., Roijers, J.F.M., van Herrewaarden, H.M.C., Lips, C.J.M., Parente, F., Quincey, D., Gaudray, P., Khodaei, S., Weber, G., Teh, B., Farnebo, F., Larsson, C., Zhang, C.X., Calender, A., Pannett, A.A.J., Forbes, S.A., Bassett, J.H.D., Thakker, R.V., Lemmens, I., Van de Ven, W.J.M., Kas, K.

“…In the process of identification of the multiple endocrine neoplasia type 1 gene, which was recently published, we isolated a novel gene in the 11q13 region…”
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A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome by HAVEN, C. J, FUNG KI WONG, LIPS, C. J, LARSSON, C, BIN TEAN TEH, MORREAU, H, VAN DAM, E. W. C. M, VAN DER LUIJT, R, VAN ASPEREN, C, JANSEN, J, ROSENBERG, C, DE WIT, M, ROIJERS, J, HOPPENER, J

“…Familial primary hyperparathyroidism is the main feature of 2 familial endocrine neoplasia syndromes: multiple endocrine neoplasia type 1 (MEN 1) and…”
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Co-metabolic degradation of chlorinated hydrocarbons by Pseudomonas sp. strain DCA1 by Hage, J.C, Kiestra, F.D.G, Hartmans, S

“…Pseudomonas sp. strain DCA1, which is capable of utilizing 1,2-dichloroethane (DCA) as sole carbon and energy source, was used to oxidize chlorinated methanes,…”
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Criteria for mutation analysis in MEN I-suspected patients: MEN I case-finding by Roijers, J F M, de Wit, M J, R B van der Luijt, H K Ploos Van Amstel

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A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome by Haven, CJ, Wong, FK, van, Dam EWCM, van, der Luijt R, van, Asperen C, Jansen, J, Rosenberg, C, de, Wit M, Roijers, J, Hoppener, J

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Multiple endocrine neoplasia type 1: recent developments and guidelines for DNA diagnosis and periodic clinical monitoring by Dreijerink, K M, Roijers, J F, van der Luijt, R B, Höppener, J W, Lips, C J

“…Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominantly inherited disorder, characterised by the occurrence of multiple tumours, particularly in…”
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Diverse expression of multiple endocrine neoplasia type 1 by Dreijerink, K M, Roijers, J F, Jansen-Schillhorn van Veen, J M, Neijt, J P, van Vroonhoven, T J, Lips, C J

“…MEN-1 is an autosomal dominantly inherited disorder, characterised by the occurrence of multiple tumours, particularly in the parathyroid glands, the…”
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A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas by Höppener, J.W.M., De Wit, M.J., Simarro-Doorten, A.Y., Roijers, J.F.M., van Herrewaarden, H.M.C., Lips, C.J.M., Parente, F., Quincey, D., Gaudray, P., Khodaei, S., Weber, G., Teh, B., Farnebo, F., Larsson, C., Zhang, C.X., Calender, A., Pannett, A.A.J., Forbes, S.A., Bassett, J.H.D., Thakker, R.V., Lemmens, I., Van de Ven, W.J.M., Kas, K.

“…In the process of identification of the multiple endocrine neoplasia type 1 gene, which was recently published, we isolated a novel gene in the 11q13 region…”
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