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1دورية أكاديمية
المؤلفون: T. C. Mangodt, K. Vanden Driessche, K. K. Norga, N. Moes, M. De Bruyne, F. Haerynck, V. Bordon, A. C. Jansen, A. I. Jonckheere
المصدر: BMC Pediatrics, Vol 23, Iss 1, Pp 1-10 (2023)
مصطلحات موضوعية: Central nervous system, LRBA deficiency, Neurological, Hearing loss, Case report, MRI, Pediatrics, RJ1-570
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2431
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2دورية أكاديمية
المؤلفون: Anne-Sophie Weyns, Annelies A.J. Verlaet, Maxim Van Herreweghe, Annelies Breynaert, Erik Fransen, Ingrid De Meester, Emilie Logie, Wim Vanden Berghe, Helene Verhelst, Dirk Van West, Ingrid Van Ingelghem, An I. Jonckheere, Diane Beysen, Sandra Kenis, Els Moens, Aalt P.J. van Roest, Huub F.J. Savelkoul, Tess De Bruyne, Luc Pieters, Berten Ceulemans, Nina Hermans
المصدر: Journal of Functional Foods, Vol 97, Iss , Pp 105247- (2022)
مصطلحات موضوعية: ADHD, French Maritime Pine Bark Extract, Methylphenidate, Oxidative stress, Immunity, Polyphenols, Nutrition. Foods and food supply, TX341-641
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Anne-Sophie Weyns, Annelies A.J. Verlaet, Annelies Breynaert, Tania Naessens, Erik Fransen, Helene Verhelst, Dirk Van West, Ingrid Van Ingelghem, An I. Jonckheere, Diane Beysen, Sandra Kenis, Els Moens, Aalt P.J. van Roest, Huub F.J. Savelkoul, Tess De Bruyne, Luc Pieters, Berten Ceulemans, Nina Hermans
المصدر: Journal of Functional Foods, Vol 97, Iss , Pp 105246- (2022)
مصطلحات موضوعية: ADHD, Behaviour, French Maritime Pine Bark Extract, Methylphenidate, Antioxidant, Polyphenols, Nutrition. Foods and food supply, TX341-641
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Sandra D. K. Kingma, Berten Ceulemans, Sandra Kenis, An I. Jonckheere
المصدر: JIMD Reports, Vol 59, Iss 1, Pp 90-103 (2021)
مصطلحات موضوعية: genotype‐phenotype, GMI gangliosidosis, intermediate phenotype, lysosomal storage disorder, Morquio type B, pathophysiology, Diseases of the endocrine glands. Clinical endocrinology, RC648-665, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2192-8312
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5
المؤلفون: An I. Jonckheere, Sandra D. K. Kingma
المصدر: Journal of inherited metabolic disease
مصطلحات موضوعية: Oncology, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Bone disease, Mucopolysaccharidosis I, Disease, Severity of Illness Index, Mucopolysaccharidosis type I, Neonatal Screening, Internal medicine, Genetics, medicine, Humans, Enzyme Replacement Therapy, skin and connective tissue diseases, Genetics (clinical), Newborn screening, business.industry, Hematopoietic Stem Cell Transplantation, Infant, Newborn, Disease Management, nutritional and metabolic diseases, Genetic Therapy, Enzyme replacement therapy, medicine.disease, Pathophysiology, Transplantation, Early Diagnosis, Phenotype, Intercellular Signaling Peptides and Proteins, Human medicine, Bone Diseases, Stem cell, business
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6
المؤلفون: An I. Jonckheere, Sandra Kenis, Berten Ceulemans, Sandra D. K. Kingma
المصدر: JIMD Reports, Vol 59, Iss 1, Pp 90-103 (2021)
JIMD Reportsمصطلحات موضوعية: Research Report, Pathology, medicine.medical_specialty, Psychomotor regression, Endocrinology, Diabetes and Metabolism, GMI gangliosidosis, intermediate phenotype, Morquio type B, Biology, Gangliosidosis, QH426-470, Biochemistry, Genetics and Molecular Biology (miscellaneous), Diseases of the endocrine glands. Clinical endocrinology, Internal Medicine, medicine, Genetics, pathophysiology, genotype‐phenotype, Ganglioside, Intermediate phenotype, Research Reports, Cherry-red spot, medicine.disease, RC648-665, Phenotype, lysosomal storage disorder, Skeletal abnormalities, medicine.symptom, Visceromegaly
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7دورية أكاديمية
المؤلفون: M. Op de Beeck, B. Gielen, I. Jonckheere, R. Samson, I. A. Janssens, R. Ceulemans
المصدر: Biogeosciences, Vol 7, Iss 1, Pp 199-215 (2010)
وصف الملف: electronic resource
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8
المؤلفون: Kim Vancampenhout, Joél Smet, Katrien Stouffs, Arnaud Vanlander, Linda De Meirleir, Rudy Van Coster, Sara Seneca, Willy Lissens, An I. Jonckheere, Boel De Paepe
المساهمون: Neurogenetics, Reproduction and Genetics, Department of Embryology and Genetics
المصدر: Vrije Universiteit Brussel
مصطلحات موضوعية: Mitochondrial DNA, Mitochondrial Diseases, mt disease, Genomics, Biology, Sensitivity and Specificity, Article, symbols.namesake, diagnostics, Genetics, Humans, Genetic Testing, Genetics (clinical), Sequence Deletion, Sanger sequencing, Massive parallel sequencing, mtDNA, Genetic Variation, High-Throughput Nucleotide Sequencing, Reproducibility of Results, Ion semiconductor sequencing, Heteroplasmy, Genome, Mitochondrial, symbols, Ion Torent PGM, Cambridge Reference Sequence, sequence heteroplasmy detection, Personal genomics
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9
المؤلفون: Martin Lammens, Merei Huigsloot, Richard J. Rodenburg, Radek Szklarczyk, Ute Spiekerkoetter, Lambert P. van den Heuvel, Martijn A. Huynen, Werner J.H. Koopman, Jürgen-Christoph von Kleist-Retzow, Marleen Forkink, Jack A.M. Fransen, Jitske Jansen, An I. Jonckheere, Jan A.M. Smeitink
المصدر: Mitochondrion, 11, 6, pp. 954-63
Mitochondrion, 11, 954-63
ResearcherIDمصطلحات موضوعية: Male, Genomic disorders and inherited multi-system disorders Energy and redox metabolism [IGMD 3], Energy and redox metabolism [NCMLS 4], Mitochondrial disease, Mitochondrion, Biology, Renal disorder Energy and redox metabolism [IGMD 9], Genomic disorders and inherited multi-system disorders [IGMD 3], Mitochondrial Proteins, Perception and Action [DCN 1], medicine, Humans, Inner mitochondrial membrane, Molecular Biology, Gene, Cells, Cultured, Renal disorder [IGMD 9], Sequence Deletion, Comparative genomics, Adenosine Triphosphatases, Genetic Complementation Test, Infant, Newborn, Mitochondrial medicine Energy and redox metabolism [IGMD 8], Membrane Proteins, Cell Biology, Immunogold labelling, Fibroblasts, Mitochondrial Proton-Translocating ATPases, medicine.disease, Mitochondrial morphology, Molecular biology, Mitochondria, Renal disorder Membrane transport and intracellular motility [IGMD 9], Complementation, Mitochondrial medicine [IGMD 8], Membrane transport and intracellular motility Renal disorder [NCMLS 5], Evaluation of complex medical interventions Auto-immunity, transplantation and immunotherapy [NCEBP 2], Energy and redox metabolism Mitochondrial medicine [NCMLS 4], Molecular Medicine, Carrier Proteins
وصف الملف: application/pdf
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10
المؤلفون: E. A. Croonen, A. I. Jonckheere, E. Morava
المصدر: Tijdschrift voor Kindergeneeskunde, 78, 197-201
Tijdschrift voor Kindergeneeskunde, 78, 5, pp. 197-201