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1. Dietetic approach to trimethylaminuria
by Alvarez, TM and Guardiola, PD and Elviro, R and Wevers, R
MEDICINA CLINICA, ISSN 0025-7753, 02/2010, Volume 134, Issue 3, pp. 134 - 135
MEDICINE, GENERAL & INTERNAL | MANAGEMENT | CHOLINE | FISH-ODOR SYNDROME | DEFICIENCY | MUTATION | Metabolism, Inborn Errors - diet therapy | Adult | Female | Metabolism, Inborn Errors - urine | Humans | Methylamines - urine
Journal Article
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2. Full Text Clinical Findings and a Therapeutic Trial in the First Patient with β-Ureidopropionase Deficiency
by Assmann, B and Göhlich, G and Baethmann, M and Wevers, R. A and Van Gennip, A. H and Van Kuilenburg, A. B. P and Dietrich, C and Wagner, L and Rotteveel, J. J and Schaper, J and Mayatepek, E and Hoffmann, G. F and Voit, T
Neuropediatrics, ISSN 0174-304X, 02/2006, Volume 37, Issue 1, pp. 20 - 25
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3. processo para fazer um artigo conformado, kit para uso em um processo para fazer um artigo conformado e artigo
by RONALD WEVERS and JACOBUS J. HOUG and FRANCISCUS J. T. KARBBENBORG and MICHAEL BALLOT
04/2012
PROCESSO PARA FAZER UM ARTIGO CONFORMADO, KIT PARA USO EM UM PROCESSO PARA FAZER UM ARTIGO CONFORMADO E ARTIGO. A presente invenção é direcionada melhorar... 
GENERAL PROCESSES OF COMPOUNDING | WORKING-UP | METALLURGY | ORGANIC MACROMOLECULAR COMPOUNDS | CHEMISTRY | THEIR PREPARATION OR CHEMICAL WORKING-UP | AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F,C08G | COMPOSITIONS OF MACROMOLECULAR COMPOUNDS | COMPOSITIONS BASED THEREON
Patent
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4. De arbeidsloopbaan van multiple sclerose patiënten
by Pelders-Wijngaard, M.T.M and Wevers, C.W.J
12/1995, Volume 3, Issue 6
Magazine Article
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5. Methodologies for metabolomics
: experimental strategies and techniques
by Sweedler, Jonathan V and Wevers, Ron, 1951 and Lutz, Norbert, 1952
2013, ISBN 9780521765909, xii, 627
"While most of the focus in "omics" science over the past decade has been on sequencing the human genome [1] or annotating the human proteome [2], there is... 
Metabolomics | Metabolites | Methodology | Mass Spectrometry | methods | Metabolic Diseases | Metabolome | diagnosis | Research | Metabolism | Mass spectrometry
Book
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6. Japan, its future, and New Zealand
: Nihon, sono shōrai to Nyū Jīrando
by Wevers, Maarten and Victoria University of Wellington. Institute of Policy Studies
1988, ISBN 0864731353, iii, 230
New Zealand Foreign relations | Japan Foreign relations
Book
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7. Yellow pencils
: contemporary poetry by New Zealand women
by Wevers, Lydia
1988, ISBN 9780195581782, xxvi, 221
New Zealand poetry
Book
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8. New Zealand short stories, fourth series
by Wevers, Lydia
1984, ISBN 9780195581096, xiii, 262
Short stories, New Zealand
Book
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9. The concept of erosion of some Belgian geologists in the 18th and 19th century
by Wevers, Joyce
1980, 154-180
Érosion | Geology
Book
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10. Full Text Localisation of pre- and postsynaptic cholinergic markers in the human brain
by Wevers, Andrea
Behavioural Brain Research, ISSN 0166-4328, 2011, Volume 221, Issue 2, pp. 341 - 355
The cholinergic neurotransmission in the central nervous system plays an important role in modulating cognitive processes such as learning, memory, arousal and... 
Choline acetyltransferase (ChAT) | Vesicular acetylcholine transporter (VAChT) | Nicotinic acetylcholine receptor (nAChR) | Muscarinic acetylcholine receptor (mAChR) | Acetylcholinesterase (AChE) | Human brain | Cholinergic transmission | MESSENGER-RNA EXPRESSION | MILD COGNITIVE IMPAIRMENT | NEUROSCIENCES | HUMAN CEREBRAL-CORTEX | POSITRON-EMISSION-TOMOGRAPHY | PARKINSONS-DISEASE STRIATUM | MICROSCOPIC AUTORADIOGRAPHIC LOCALIZATION | NICOTINIC ACETYLCHOLINE-RECEPTOR | HUMAN FRONTAL-CORTEX | BEHAVIORAL SCIENCES | CENTRAL-NERVOUS-SYSTEM | HEMICHOLINIUM-3 BINDING-SITES | Brain | Choline
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11. Text history of the Greek Leviticus
by Wevers, John William
1986, Abhandlungen der Akademie der Wissenschaften in Göttingen. Philologisch-Historische Klasse, ISBN 9783525824405, Volume 3. Folge, Nr. 153, 136
Bible. VersionsSeptuagint | Bible. Criticism, Textual
Book
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12. Full Text Exome Sequencing and the Management of Neurometabolic Disorders
by Tarailo-Graovac, Maja and Shyr, Casper and Ross, Colin J and Horvath, Gabriella A and Salvarinova, Ramona and Ye, Xin C and Zhang, Lin-Hua and Bhavsar, Amit P and Lee, Jessica J.Y and Drögemöller, Britt I and Abdelsayed, Mena and Alfadhel, Majid and Armstrong, Linlea and Baumgartner, Matthias R and Burda, Patricie and Connolly, Mary B and Cameron, Jessie and Demos, Michelle and Dewan, Tammie and Dionne, Janis and Evans, A. Mark and Friedman, Jan M and Garber, Ian and Lewis, Suzanne and Ling, Jiqiang and Mandal, Rupasri and Mattman, Andre and McKinnon, Margaret and Michoulas, Aspasia and Metzger, Daniel and Ogunbayo, Oluseye A and Rakic, Bojana and Rozmus, Jacob and Ruben, Peter and Sayson, Bryan and Santra, Saikat and Schultz, Kirk R and Selby, Kathryn and Shekel, Paul and Sirrs, Sandra and Skrypnyk, Cristina and Superti-Furga, Andrea and Turvey, Stuart E and Van Allen, Margot I and Wishart, David and Wu, John and Wu, Jiang and Zafeiriou, Dimitrios and Kluijtmans, Leo and Wevers, Ron A and Eydoux, Patrice and Lehman, Anna M and Vallance, Hilary and Stockler-Ipsiroglu, Sylvia and Sinclair, Graham and Wasserman, Wyeth W and van Karnebeek, Clara D
The New England Journal of Medicine, ISSN 0028-4793, 06/2016, Volume 374, Issue 23, pp. 2246 - 2255
In this study, whole-exome sequencing was used as the basis for providing a diagnosis in 47 probands with intellectual developmental disorder and unexplained... 
INTELLECTUAL DISABILITY | INFANTILE ONSET | RARE-DISEASE | MEDICINE, GENERAL & INTERNAL | PRESENTS | GENE-DISCOVERY | MUTATIONS | SPECTRUM | DEFICIENCY | Humans | Child, Preschool | Genotype | Infant | Male | Genetic Testing - methods | Metabolism, Inborn Errors - genetics | Intellectual Disability - genetics | Exome | Young Adult | Metabolism, Inborn Errors - diagnosis | Phenotype | Adolescent | Adult | Female | Child | Sequence Analysis, DNA - methods | Nervous system diseases | Care and treatment | Genetic aspects | Research | Exome sequencing | Phenotypes | Inborn errors of metabolism | Intellectual disabilities | Genomics | Phenotyping | Disease management | Children | Diagnosis | Metabolism | Bioinformatics | Patients | Metabolic disorders
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13. Full Text Autosomal Recessive Dilated Cardiomyopathy due to DOLK Mutations Results from Abnormal Dystroglycan O-Mannosylation
by Lefeber, D.J and Brouwer, A.P.M. de and Morava, E and Riemersma, M and Schuurs-Hoeijmakers, J.H.M and Absmanner, B and Verrijp, K and Akker, W.M.R. van den and Huijben, K and Steenbergen, G.C and Reeuwijk, J. van and Jozwiak, A and Zucker, N and Lorber, A and Lammens, M.M.Y and Knopf, C and Bokhoven, H. van and Grunewald, S and Lehle, L and Kapusta, L and Mandel, H and Wevers, R.A
Plos Genetics, ISSN 1553-7404, 2011, Volume 7, Issue 12, pp. e1002427 - e1002427
Genetic causes for autosomal recessive forms of dilated cardiomyopathy (DCM) are only rarely identified, although they are thought to contribute considerably... 
PHOSPHATE | HYPERTROPHIC CARDIOMYOPATHY | PROTEIN | GLYCOSYLATION TYPE IA | DOLICHOL KINASE | PHOSPHORYLATION | BIOSYNTHESIS | CAUSES CONGENITAL DISORDER | GENETICS & HEREDITY | SACCHAROMYCES-CEREVISIAE | ASSOCIATION | Cardiomyopathy, Dilated - genetics | Haplotypes | Gene Expression | Saccharomyces cerevisiae - genetics | Humans | Phosphotransferases (Alcohol Group Acceptor) - deficiency | Child, Preschool | Dystroglycans - metabolism | Male | Phosphotransferases (Alcohol Group Acceptor) - genetics | Glycosylation | Cardiomyopathy, Dilated - metabolism | Genes, Recessive | Homozygote | Dolichol Phosphates - metabolism | Pedigree | Adolescent | Female | Child | Sarcolemma - metabolism | Laminin | Gene mutations | Physiological aspects | Genetic aspects | Research | Cardiomyopathy, Dilated | Proteins | Medical research | Genetics | Zebrafish | Mutation | Rodents
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14. Essays on the ancient Semitic world
by Wevers, John William and Redford, Donald B
1970, Toronto Semitic texts and studies, ISBN 0802016030, vii, 112
Hebrew language | Semitic philology | Vocalization
Book
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15. Full Text Multiple Phenotypes in Phosphoglucomutase 1 Deficiency
by Tegtmeyer, Laura C and Rust, Stephan and van Scherpenzeel, Monique and Ng, Bobby G and Losfeld, Marie-Estelle and Timal, Sharita and Raymond, Kimiyo and He, Ping and Ichikawa, Mie and Veltman, Joris and Huijben, Karin and Shin, Yoon S and Sharma, Vandana and Adamowicz, Maciej and Lammens, Martin and Reunert, Janine and Witten, Anika and Schrapers, Esther and Matthijs, Gert and Jaeken, Jaak and Rymen, Daisy and Stojkovic, Tanya and Laforêt, Pascal and Petit, François and Aumaître, Olivier and Czarnowska, Elzbieta and Piraud, Monique and Podskarbi, Teodor and Stanley, Charles A and Matalon, Reuben and Burda, Patricie and Seyyedi, Soraya and Debus, Volker and Socha, Piotr and Sykut-Cegielska, Jolanta and van Spronsen, Francjan and de Meirleir, Linda and Vajro, Pietro and DeClue, Terry and Ficicioglu, Can and Wada, Yoshinao and Wevers, Ron A and Vanderschaeghe, Dieter and Callewaert, Nico and Fingerhut, Ralph and van Schaftingen, Emile and Freeze, Hudson H and Morava, Eva and Lefeber, Dirk J and Marquardt, Thorsten
The New England Journal of Medicine, ISSN 0028-4793, 02/2014, Volume 370, Issue 6, pp. 533 - 542
Two brothers with an undefined congenital disorder of glycosylation were found to have phosphoglucomutase 1 deficiency, which has previously been described as... 
MUSCLE GLYCOGENOSIS | MEDICINE, GENERAL & INTERNAL | THERAPY | GLYCOGEN-STORAGE-DISEASE | GLUCOSE | NUCLEOTIDE SUGARS | CONGENITAL DISORDERS | DILATED CARDIOMYOPATHY | GLYCOSYLATION | IDENTIFICATION | CHILDREN | Physiological aspects | Glycosylation | Genetic aspects | Genetic disorders | Research | Phosphoglucomutase | Growth rate | Cardiomyopathy | Genotype & phenotype | Polysaccharides | Glycogenosis | Enzymatic activity | Metabolites | Fibroblasts | Carbohydrates | Enzymes | Phenotypes | Congenital diseases | Malignant hyperthermia | Glycogen | Dietary supplements | Mass spectroscopy | N-glycans | Hypoglycemia | Hypogonadism | Hereditary diseases | Dilated cardiomyopathy | Mutation | Gene mapping | Galactose | Hyperthermia | Myopathy
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16. Full Text How metal-tolerant ecotypes of ectomycorrhizal fungi protect plants from heavy metal pollution
by Colpaert, Jan V and Wevers, Jan H.L and Krznaric, Erik and Adriaensen, Kristin
Annals of Forest Science, ISSN 1286-4560, 1/2011, Volume 68, Issue 1, pp. 17 - 24
Heavy metal pollution is a strong driver of above- and belowground communities and triggers evolutionary adaptation in organisms. This review provides an... 
Life Sciences | Environment, general | Heavy metal tolerance | Wood Science & Technology | Heavy metal pollution | Suillus luteus | Forestry | Forestry Management | Tree Biology | Pinus sylvestris | Ectomycorrhizal fungi | PRIMARY SUCCESSION | PINUS-SYLVESTRIS | SACCHAROMYCES-CEREVISIAE | PAXILLUS-INVOLUTUS | MYCORRHIZAL FUNGI | ADAPTIVE TOLERANCE | IN-VITRO | DIFFERENTIAL RESPONSES | TOXIC METALS | FORESTRY | SUILLUS-LUTEUS | Agricultural sciences | Silviculture, forestry
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17. Full Text Four-month metacarpal bone mineral density loss predicts radiological joint damage progression after 1 year in patients with early rheumatoid arthritis: exploratory analyses from the IMPROVED study
by Boer, K V C Wevers-de and Heimans, L and Visser, K and Kälvesten, J and Goekoop, R J and van Oosterhout, M and Harbers, J B and Bijkerk, C and Steup-Beekman, M and de Buck, M P D M and de Sonnaville, P B J and Huizinga, T W J and Allaart, C F and Linköpings universitet and Centrum för medicinsk bildvetenskap och visualisering, CMIV
Annals of the Rheumatic Diseases, ISSN 0003-4967, 02/2015, Volume 74, Issue 2, pp. 341 - 346
Aim To assess whether in early (rheumatoid) arthritis (RA) patients, metacarpal bone mineral density (BMD) loss after 4 months predicts radiological... 
RISK MODEL | TREATMENT STRATEGIES | X-RAY RADIOGRAMMETRY | RHEUMATOLOGY | SIMULATION | PREDNISOLONE | ASSOCIATION | UNDIFFERENTIATED ARTHRITIS | RAPID RADIOGRAPHIC PROGRESSION | DISEASE-ACTIVITY | REMISSION | Hydroxychloroquine - therapeutic use | Sulfasalazine - therapeutic use | Bone Density | Humans | Middle Aged | Male | Methotrexate - therapeutic use | Absorptiometry, Photon | Disease Progression | Arthritis, Rheumatoid - pathology | Arthritis, Rheumatoid - diagnostic imaging | Metacarpal Bones - diagnostic imaging | Arthritis, Rheumatoid - drug therapy | Female | Prednisone - therapeutic use | Antirheumatic Agents - therapeutic use | Care and treatment | Rheumatoid arthritis | Analysis | Radiology | Bones | Radiology, Medical | Density | Studies | Variables | Clinical trials | Bone density | Soil erosion | Clinical medicine | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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18. Full Text Cerebrospinal fluid glucose and lactate: age-specific reference values and implications for clinical practice
by Leen, W.G and Willemsen, M.A.A.P and Wevers, R.A and Verbeek, M.M
PLoS One, ISSN 1932-6203, 2012, Volume 7, Issue 8, p. e42745
Cerebrospinal fluid (CSF) analysis is an important tool in the diagnostic work-up of many neurological disorders, but reference ranges for CSF glucose,... 
PROTEIN-CONCENTRATION | GLUT1 | BACTERIAL-MENINGITIS | INFANTS | BIOLOGY | DISORDERS | RATIO | MUTATIONS | DEFICIENCY | CHILDREN | Humans | Middle Aged | Child, Preschool | Infant | Reference Values | Practice Patterns, Physicians | Aging - cerebrospinal fluid | Glucose - cerebrospinal fluid | Young Adult | Lactic Acid - cerebrospinal fluid | Adolescent | Aged, 80 and over | Adult | Aged | Blood Glucose - metabolism | Child | Infant, Newborn | Glycosylated hemoglobin | Nervous system diseases | Glucose | Dextrose | Neonates | Laboratories | Nervous system | Cerebrospinal fluid | Bilirubin | Hypoglycemia | Metabolism | Patients | Data bases | Neurological diseases | Proteins | Neurology | Hyperglycemia | Red blood cells | Cognition & reasoning | Diagnostic software | Hemoglobin | Meningitis | Diagnostic systems | Lactic acid | Clinical medicine | Mutation | Age
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