-
1
المؤلفون: Therese Rosenling, Alain J. van Gool, Sybren S. Wijmenga, Rob J. Vreeken, Bas Muilwijk, Adrie Dane, Theo M. Luider, Lutgarde M. C. Buydens, Peter Horvatovich, Shanna Shi, Christin Christin, Agnieszka Smolinska, Marcel P. Stoop, Thomas Hankemeier, Frank Suits, Rainer Bischoff, Leon Coulier
المساهمون: Neurology, Epidemiology, Molecular Genetics, Analytical Biochemistry, Groningen Research Institute of Pharmacy, Medicinal Chemistry and Bioanalysis (MCB)
المصدر: Clinical Chemistry, 57(12), 1703-1711. American Association for Clinical Chemistry Inc.
Clinical Chemistry, 57, 1703-1711
Clinical Chemistry, 57, 12, pp. 1703-11
Clinical Chemistry, 57(12), 1703-1711. AMER ASSOC CLINICAL CHEMISTRY
Clinical Chemistry, 57, 12, pp. 1703-1711
Clinical Chemistry, 57, 1703-11
Clinical Chemistry, 12, 57, 1703-1711مصطلحات موضوعية: Chromatography, Gas, Magnetic Resonance Spectroscopy, Time Factors, Proteome, Metabolite, BLOOD-SERUM, Clinical Biochemistry, CSF, Mass Spectrometry, Specimen Handling, Analytical Chemistry, chemistry.chemical_compound, Blood serum, Metabolomics, SDG 3 - Good Health and Well-being, EELS - Earth, Environmental and Life Sciences TNO Bedrijven, CYSTATIN-C, Metabolome, Humans, QS - Quality & Safety AR - Analytical Research, Cerebrospinal Fluid, Nutrition, Chromatography, STABILITY, Chemistry, Biochemistry (medical), Selected reaction monitoring, Life Triskelion BV, MULTIPLE-SCLEROSIS, MASS-SPECTROMETRY, Glycostation disorders [IGMD 4], Ascorbic acid, BIOMARKER DISCOVERY, Biochemistry, ASCORBIC-ACID, NMR-SPECTROSCOPY, Sample collection, Biophysical Chemistry, LIQUID-CHROMATOGRAPHY, Functional Neurogenomics [DCN 2], Healthy Living, Chromatography, Liquid
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f237008644d12dc3fd3a14f8fa34deTest
https://doi.org/10.1373/clinchem.2011.167601Test -
2
المؤلفون: Jorieke E. H. Bergman, Vincent Cantagrel, Jeroen Schoots, Dirk J. Lefeber, Michèl A.A.P. Willemsen, Peter Bluemel, Christian Körner, Ron A. Wevers, Georg F. Hoffmann, Bobby G. Ng, Karin Huijben, Connie M. A. van Ravenswaaij-Arts, Maciej Adamowicz, Hans van Bokhoven, Dusica Babovic-Vuksanovic, Arjan P.M. de Brouwer, Arno van Rooij, Lihadh Al-Gazali, Jeroen van Reeuwijk, Eva Morava, Marjolein C. J. Jongmans, Ludwig Lehle, Jolanta Sykut-Cegielska, Lies H. Hoefsloot, Joseph G. Gleeson
المساهمون: Reproductive Origins of Adult Health and Disease (ROAHD)
المصدر: Brain, 133, 11, pp. 3210-20
Brain, 133, 3210-3220. Oxford University Press
Brain, 133, 3210-20مصطلحات موضوعية: Male, Pathology, Glycosylation, Polyprenol reductase, Genetics and epigenetic pathways of disease [NCMLS 6], Eye Diseases, Neuroinformatics [DCN 3], CHARGE syndrome, chemistry.chemical_compound, Dolichols, dolichol metabolism, Child, Cerebellar hypoplasia, JOUBERT-SYNDROME, SRD5A3-CDG, Homozygote, polyprenol reductase, Syndrome, Hypoplasia, CDG type Iq, cataract, CHARGE-SYNDROME, Child, Preschool, coloboma, Female, lipids (amino acids, peptides, and proteins), medicine.symptom, Functional Neurogenomics [DCN 2], medicine.medical_specialty, CONGENITAL DISORDERS, Biology, Joubert syndrome, Genomic disorders and inherited multi-system disorders [IGMD 3], Abnormal glycosylation, Dolichol, 3-Oxo-5-alpha-Steroid 4-Dehydrogenase, Cerebellar Diseases, Internal medicine, medicine, Humans, BIOSYNTHESIS, SPECTRUM, Cerebellar ataxia, MUTATIONS, vermis hypoplasia, Infant, Membrane Proteins, Original Articles, Glycostation disorders [IGMD 4], Lipid Metabolism, medicine.disease, GENE, carbohydrates (lipids), glaucoma, Endocrinology, chemistry, Mutation, SRD5A3, CDG, Neurology (clinical), AUTOSOMAL RECESSIVE SYNDROME, MENTAL-RETARDATION, congenital disorders of glycosylation, Microsatellite Repeats
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bea1dc7bce4c935f88e51dacb8481f2dTest
https://doi.org/10.1093/brain/awq261Test -
3
المؤلفون: J. Hayek, Monique J. B. M. Veendrick-Meekes, Maria Tassini, Raffaella Zannolli, Maaike de Vries, Appie Bilos, Gianni Valensin, Ron A. Wevers, Eva Morava, Udo F. H. Engelke, Leo A. J. Kluijtmans, Antonio Vivi, Wim Brussel, Sabrina Buoni, Berry Kremer, Gajja S. Salomons
المساهمون: Internal Medicine Specializations, Clinical chemistry, Other Research
المصدر: Engelke, U F H, Tassini, M, Hayek, J, de Vries, M, Bilos, A, Vivi, A, Valensin, G, Buoni, S, Zannolli, R, Brussel, W, Kremer, B, Salomons, G S, Veendrick-Meekes, M J B M, Kluijtmans, L A J, Morava, E & Wevers, R A 2009, ' Guanidinoacetate methyltransferase (GAMT) deficiency diagnosed by proton NMR spectroscopy of body fluids ', NMR in Biomedicine, vol. 22, no. 5, pp. 538-544 . https://doi.org/10.1002/nbm.1367Test
NMR in Biomedicine, 22, 538-44
NMR in Biomedicine, 22(5), 538-544. John Wiley and Sons Ltd
NMR in Biomedicine, 22, 5, pp. 538-44مصطلحات موضوعية: Adult, Male, Magnetic Resonance Spectroscopy, creatine biosynthesis, Energy and redox metabolism [NCMLS 4], Glycine, Membrane transport and intracellular motility [NCMLS 5], L-arginine, in vitro (1)H NMR spectroscopy, Urine, Creatine, guanidinoacetate methyltransferase, Genomic disorders and inherited multi-system disorders [IGMD 3], chemistry.chemical_compound, Cerebrospinal fluid, Reference Values, guanidino-acetic acid, glycine amidinotransferase, Humans, Radiology, Nuclear Medicine and imaging, Child, Spectroscopy, Creatinine, Chromatography, creatinine, Infant, Nuclear magnetic resonance spectroscopy, Hydrogen-Ion Concentration, Glycostation disorders [IGMD 4], Body Fluids, Guanidinoacetate N-methyltransferase, NMR spectra database, creatine, chemistry, Child, Preschool, Proton NMR, Molecular Medicine, Female, Guanidinoacetate N-Methyltransferase, Protons, Functional Neurogenomics [DCN 2]
وصف الملف: application/pdf; Print
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65ad2489fa250e140ba7b4aa57fe2193Test
https://doi.org/10.1002/nbm.1367Test -
4
المؤلفون: Ron A. Wevers, Christine R. Kaneski, Udo F. H. Engelke, Jiahuan Ding, Julie Barritault, Nathan McNeill, Raphael Schiffmann, Fanny Mochel, Marjan Huizing, Mones Abu-Asab, David R. Adams, François Seguin, Bingzhi Yang, Frans W. Verheijen, William S. Benko, Jerry N. Thompson, Maria Tsokos
المساهمون: Clinical Genetics
المصدر: Annals of Neurology, 65, 6, pp. 753-7
Annals of Neurology, 65, 753-7
Annals of Neurology, 65(6), 753-757. John Wiley & Sons Inc.مصطلحات موضوعية: Sialuria, medicine.medical_specialty, Adolescent, Energy and redox metabolism [NCMLS 4], Organic anion transporter 1, Organic Anion Transporters, Urine, medicine.disease_cause, Article, Diagnosis, Differential, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, chemistry.chemical_compound, Cerebrospinal fluid, Internal medicine, medicine, Humans, Child, Nuclear Magnetic Resonance, Biomolecular, Mutation, Symporters, biology, Sialic Acid Storage Disease, Glycostation disorders [IGMD 4], medicine.disease, N-Acetylneuraminic Acid, Sialic acid, Hereditary Central Nervous System Demyelinating Diseases, Endocrinology, Neurology, chemistry, biology.protein, Neurology (clinical), Functional Neurogenomics [DCN 2], N-Acetylneuraminic acid
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec13ae7461e98be4f002f7c42730d09Test
https://doi.org/10.1002/ana.21624Test -
5
المؤلفون: Barbara Franke, Mascha M.V.A.P. Schijvenaars, Martin den Heijer, Hans Scheffer, Marieke J H Coenen, Sita H. Vermeulen, Régine P.M. Steegers-Theunissen, Henk J. Blom
المساهمون: Laboratory Medicine, ICaR - Ischemia and repair
المصدر: Franke, B, Vermeulen, S H, Steegers-Theunissen, R P, Coenen, M J, Schijvenaars, M M V A, Scheffer, H, den Heijer, M & Blom, H J 2009, ' An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1) ', Birth Defects Research Part A-Clinical and Molecular Teratology, vol. 85, no. 3, pp. 216-226 . https://doi.org/10.1002/bdra.20556Test
Birth Defects Research Part A-Clinical and Molecular Teratology, 85, 3, pp. 216-26
Birth Defects Research Part A-Clinical and Molecular Teratology, 85(3), 216-226. Wiley-Liss Inc.
Birth Defects Research Part A-Clinical and Molecular Teratology, 85, 216-26مصطلحات موضوعية: Embryology, Candidate gene, congenital, hereditary, and neonatal diseases and abnormalities, Genotype, Energy and redox metabolism [NCMLS 4], Genetics and epigenetic pathways of disease [NCMLS 6], Receptors, Cell Surface, Single-nucleotide polymorphism, Neuroinformatics [DCN 3], Biology, RFC1, Cobalamin, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], chemistry.chemical_compound, Folic Acid, Translational research [ONCOL 3], Perception and Action [DCN 1], medicine, Humans, DNA (Cytosine-5-)-Methyltransferases, Cyanocobalamin, Child, Spinal Dysraphism, Genetics, Polymorphism, Genetic, Spina bifida, Hormonal regulation [IGMD 6], Neural tube, General Medicine, Glycostation disorders [IGMD 4], Cubilin, medicine.disease, nervous system diseases, medicine.anatomical_structure, chemistry, Pediatrics, Perinatology and Child Health, Female, Functional Neurogenomics [DCN 2], Developmental Biology
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15811c07f4242b2de0dd1e3a1b4f9484Test
https://doi.org/10.1002/bdra.20556Test -
6
المؤلفون: Björn Fischer, Aikaterini Dimopoulou, Uwe Kornak, Eva Morava, Maïlys Guillard, Dirk J. Lefeber, Ron A. Wevers
المصدر: Biochimica et Biophysica Acta. Molecular Basis of Disease, 1792, 903-14
Biochimica et Biophysica Acta. Molecular Basis of Disease, 1792, 9, pp. 903-14مصطلحات موضوعية: Models, Molecular, Vacuolar Proton-Translocating ATPases, Glycosylation, Energy and redox metabolism [NCMLS 4], Occipital horn syndrome, OMIM 219200, V-ATPase, Genes, Recessive, Biology, Cutis Laxa, 03 medical and health sciences, chemistry.chemical_compound, Mice, 0302 clinical medicine, Congenital Disorders of Glycosylation, Apolipoprotein C III, medicine, Animals, Humans, Molecular Biology, Gene, 030304 developmental biology, Genetics, 0303 health sciences, Apolipoprotein C-III, Cell Membrane, Transferrin, Glycostation disorders [IGMD 4], medicine.disease, Phenotype, 3. Good health, Protein Subunits, Proton-Translocating ATPases, chemistry, Molecular Medicine, Functional Neurogenomics [DCN 2], 030217 neurology & neurosurgery, Cutis laxa, Subcellular Fractions
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c81bb80275980e7ddd9dc08e12b9f6caTest
https://doi.org/10.1016/j.bbadis.2008.12.009Test -
7
المؤلفون: Eva Morava, Jolein Gloerich, Maïlys Guillard, Dirk J. Lefeber, Hans J. C. T. Wessels, Ron A. Wevers
المصدر: Carbohydrate Research, 344, 1550-7
Carbohydrate Research, 344, 12, pp. 1550-7مصطلحات موضوعية: Spectrum analyzer, Glycan, Glycosylation, Energy and redox metabolism [NCMLS 4], Coumaric Acids, Molecular Sequence Data, Analytical chemistry, Mass spectrometry, Biochemistry, Analytical Chemistry, chemistry.chemical_compound, Polysaccharides, Exoglycosidase, Humans, Quadrupole ion trap, Reproducibility, Chromatography, biology, Organic Chemistry, Reproducibility of Results, General Medicine, Glycostation disorders [IGMD 4], Carbohydrate Sequence, chemistry, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, biology.protein, Ion trap, Functional Neurogenomics [DCN 2]
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f73776c4cffbee8292788aa7cc9b40Test
https://hdl.handle.net/2066/80369Test -
8
المؤلفون: Bart W. Smits, Baziel G. M. van Engelen, Rob C.A. Sengers, Jan A.M. Smeitink, Marjo S. van der Knaap, Marloes H. Siers, Richard J. Rodenburg, Frans J.M. Trijbels, Francjan J. van Spronsen, Liesbeth T. Wintjes, Markus Schuelke, Barbara Lucke, Eva Morava, Henk J. ter Laak, Antoon J.M. Janssen, Lambert P. van den Heuvel, Frans A. Hol
المساهمون: Pediatric surgery, Neuroscience Campus Amsterdam 2008, Other departments, Faculteit Medische Wetenschappen/UMCG, Center for Liver, Digestive and Metabolic Diseases (CLDM)
المصدر: Annals of Neurology, 63(4), 473-481. John Wiley and Sons Inc.
Annals of Neurology, 63, 473-81
Annals of neurology, 63(4), 473-481. John Wiley and Sons Inc.
Janssen, A J M, Schuelke, M, Smeitink, J A M, Trijbels, F J M, Sengers, R C A, Lucke, B, Wintjes, L T M, Morava, E, van Engelen, B G M, Smits, B W, Hol, F A, Siers, M H, Ter Laak, H, van der Knaap, M S, van Spronsen, F J, Rodenburg, R J T & van den Heuvel, L P 2008, ' Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system ', Annals of Neurology, vol. 63, no. 4, pp. 473-481 . https://doi.org/10.1002/ana.21328Test
Annals of Neurology, 63(4), 473-481. Wiley
Annals of Neurology, 63, 4, pp. 473-81مصطلحات موضوعية: Male, Adenosine, genetic structures, Respiratory chain, Mitochondrion, medicine.disease_cause, chemistry.chemical_compound, Mitochondrial myopathy, OXIDATIVE-PHOSPHORYLATION, Perception and Action [DCN 1], MELAS Syndrome, Child, LACTIC-ACIDOSIS, Human Movement & Fatigue [NCEBP 10], Mutation, Middle Aged, Mitochondrial medicine [IGMD 8], Neurology, Biochemistry, Child, Preschool, Lactic acidosis, SKELETAL-MUSCLE, Female, Functional Neurogenomics [DCN 2], psychological phenomena and processes, Adult, Mitochondrial DNA, Guanine, Energy and redox metabolism [NCMLS 4], Adolescent, Oxidative phosphorylation, Biology, DNA, Mitochondrial, behavioral disciplines and activities, COMPLEX-I, TRNA(LEU(UUR)) MUTATION, Genomic disorders and inherited multi-system disorders [IGMD 3], Electron Transport, Translational research [ONCOL 3], medicine, Humans, Muscle, Skeletal, A3243G POINT MUTATION, CLINICAL-FEATURES, STROKE-LIKE EPISODES, Infant, DELAYED DIAGNOSIS, Glycostation disorders [IGMD 4], medicine.disease, Neuromuscular development and genetic disorders [UMCN 3.1], TRANSFER RNALEU(UUR) GENE, Mitochondria, Muscle, Genetic defects of metabolism [UMCN 5.1], chemistry, nervous system, Neurology (clinical), Cellular energy metabolism [UMCN 5.3], Energy Metabolism, Adenosine triphosphate
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7309e350811f28f7884ed308e7f876feTest
https://hdl.handle.net/11370/e6d330f9-2287-4630-80cc-c24222097463Test -
9
المؤلفون: Frans J.M. Trijbels, Liesbeth T. Wintjes, Wim Ruitenbeek, Antoon J.M. Janssen, Lambert P. van den Heuvel, Richard J. Rodenburg, Rob C.A. Sengers, Jan A.M. Smeitink, Eva Morava, Baziel G.M. van Engelen
المصدر: Clinical Chemistry, 52, 860-71
Clinical Chemistry, 52, 5, pp. 860-71مصطلحات موضوعية: Adult, Male, Pyruvate decarboxylation, Mitochondrial Diseases, Pyruvate dehydrogenase kinase, Energy and redox metabolism [NCMLS 4], Adolescent, Biopsy, Clinical Biochemistry, Malates, Succinic Acid, Pyruvate Dehydrogenase Complex, Pyruvate dehydrogenase phosphatase, Biology, Oxidative Phosphorylation, Genomic disorders and inherited multi-system disorders [IGMD 3], chemistry.chemical_compound, Adenosine Triphosphate, Translational research [ONCOL 3], Carnitine, Pyruvic Acid, Humans, Carbon Radioisotopes, Dihydrolipoyl transacetylase, Child, Muscle, Skeletal, Human Movement & Fatigue [NCEBP 10], Biochemistry (medical), Glycostation disorders [IGMD 4], Pyruvate dehydrogenase complex, Neuromuscular development and genetic disorders [UMCN 3.1], Malonates, Mitochondria, Pyruvate carboxylase, Citric acid cycle, Mitochondrial medicine [IGMD 8], chemistry, Biochemistry, Child, Preschool, Female, Pyruvic acid, Cellular energy metabolism [UMCN 5.3], Energy Metabolism, Functional Neurogenomics [DCN 2], Mitochondrial ADP, ATP Translocases, Oxidation-Reduction
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f25756668e3dc458d21c7e61b2642028Test
https://doi.org/10.1373/clinchem.2005.062414Test -
10
المؤلفون: H. Zweers van Essen, Saskia B. Wortmann, Eva Morava, R. Liebrand van Sambeek, O. P. van Diggelen, Ron A. Wevers
المساهمون: Clinical Genetics
المصدر: Journal of Inherited Metabolic Disease, 28, 5, pp. 703-6
Journal of Inherited Metabolic Disease, 28, 703-6
Journal of Inherited Metabolic Disease, 28(5), 703-706. Springer Netherlandsمصطلحات موضوعية: Male, Heterozygote, medicine.medical_specialty, Erythrocytes, Energy and redox metabolism [NCMLS 4], Phosphorylase Kinase, Butanols, Urinary system, Oligosaccharides, 1-Propanol, Urine, Neuroinformatics [DCN 3], Biology, Biochemistry, High cholesterol, Genomic disorders and inherited multi-system disorders [IGMD 3], Excretion, Hemoglobins, chemistry.chemical_compound, Glucosides, Internal medicine, Perception and Action [DCN 1], Genetics, medicine, Humans, Glycogen storage disease, Phosphorylase kinase, Genetics (clinical), Family Health, Triglyceride, Glycostation disorders [IGMD 4], Glycogen Storage Disease, medicine.disease, Neuromuscular development and genetic disorders [UMCN 3.1], Quality of Care [EBP 4], Mitochondrial medicine [IGMD 8], Cholesterol, Endocrinology, Genetic defects of metabolism [UMCN 5.1], chemistry, Female, lipids (amino acids, peptides, and proteins), Chromatography, Thin Layer, Growth delay, Functional Neurogenomics [DCN 2], Blood Chemical Analysis
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d847a4f35d29dae3f9f1d5f3de7fb14Test
https://doi.org/10.1007/s10545-005-0095-9Test