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1دورية أكاديمية
المؤلفون: DJM, Bergen, A, Maurizi, MM, Formosa, GLK, McDonald, A, El-Gazzar, N, Hassan, ML, Brandi, JA, Riancho, F, Rivadeneira, E, Ntzani, EL, Duncan, CL, Gregson, DP, Kiel, MC, Zillikens, L, Sangiorgi, W, Hogler, I, Duran, O, Makitie, W, Van Hul, G, Hendrickx
المصدر: Yearbook of Paediatric Endocrinology ; ISSN 1662-4009
مصطلحات موضوعية: General Earth and Planetary Sciences, General Environmental Science
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المؤلفون: W. Van Hul, Zhanna E. Belaya, M Vorontsova, Olga O. Golounina, I Shafieva, E Mamedova, I Demina, N Tarbaeva, Alexey Nikitin, E Pigarova
المصدر: Osteoporosis international
مصطلحات موضوعية: 0301 basic medicine, Bone mineral, medicine.medical_specialty, business.industry, Endocrinology, Diabetes and Metabolism, Hyperkeratosis, Bone marrow failure, 030209 endocrinology & metabolism, Gene mutation, medicine.disease, Rheumatology, Surgery, 03 medical and health sciences, 0302 clinical medicine, Zoledronic acid, Internal medicine, Orthopedic surgery, medicine, Human medicine, 030101 anatomy & morphology, business, Dyskeratosis congenita, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae3c40509a77c5df48344cdc900af248Test
https://doi.org/10.1007/s00198-020-05758-6Test -
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المؤلفون: Z, Belaya, O, Golounina, A, Nikitin, N, Tarbaeva, E, Pigarova, E, Mamedova, M, Vorontsova, I, Shafieva, I, Demina, W, Van Hul
المصدر: Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA. 32(6)
مصطلحات موضوعية: Adult, Male, Young Adult, Adolescent, Hip Fractures, Child, Preschool, Exoribonucleases, Mutation, Humans, Bone Marrow Failure Disorders, Telomere, Dyskeratosis Congenita
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::c3671a5087adc66ac9d776b9086e4791Test
https://pubmed.ncbi.nlm.nih.gov/33244623Test -
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المؤلفون: M.E.C. Meuwissen, Ellen Geets, W. Van Hul
المصدر: Clinical genetics
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Genetic counseling, Population, Genetic Counseling, Disease, 030105 genetics & heredity, Bioinformatics, Wilms Tumor, 03 medical and health sciences, Bardet–Biedl syndrome, Intellectual Disability, Molecular genetics, Genetics, medicine, Humans, Obesity, education, Aniridia, Bardet-Biedl Syndrome, Biology, Alstrom Syndrome, Genetics (clinical), education.field_of_study, business.industry, High-Throughput Nucleotide Sequencing, Wilms' tumor, medicine.disease, Phenotype, 030104 developmental biology, Human medicine, business, Prader-Willi Syndrome, Alström syndrome
وصف الملف: pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec94bc70d914cc09b3c97d07e1aa9c2Test
https://doi.org/10.1111/cge.13367Test -
5دورية أكاديمية
المؤلفون: K Janssens, F Vanhoenacker, M Bonduelle, L Verbruggen, L Van Maldergem, S Ralston, N Migone, S Wientroub, M T Divizia, C Bergmann, C Bennett, S Simsek, T Cundy, W Van Hul
المساهمون: The Pennsylvania State University CiteSeerX Archives
مصطلحات موضوعية: Correspondence to
وصف الملف: application/pdf
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المؤلفون: Peter Michielsen, E. Van Marck, Doreen Zegers, Sven Francque, M. Ruppert, Sandrine Caron, L. Van Gaal, Bart Staels, Marja-Riitta Taskinen, Guy Hubens, An Verrijken, Sigri Beckers, W. Van Hul, H. Hilden
المصدر: Obesity. 21:2138-2145
مصطلحات موضوعية: education.field_of_study, medicine.medical_specialty, Nutrition and Dietetics, medicine.diagnostic_test, business.industry, Endocrinology, Diabetes and Metabolism, Population, Fatty liver, Medicine (miscellaneous), medicine.disease, Endocrinology, Insulin resistance, Internal medicine, Liver biopsy, medicine, Apolipoprotein C3, Adiponutrin, Steatohepatitis, Steatosis, education, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::cb3a0d54bda43ac2d80270756578d223Test
https://doi.org/10.1002/oby.20366Test -
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المؤلفون: W. Van Hul, Vere Borra, Robert J. Stokroos, Johannes J. Manni, J.J. Waterval
المساهمون: MUMC+: MA Keel Neus Oorheelkunde (9), KNO, RS: MHeNs School for Mental Health and Neuroscience
المصدر: Calcified tissue international
Calcified Tissue International, 93(1), 93-100. Springer, Chamمصطلحات موضوعية: Adult, Male, Hyperostosis, Candidate gene, Pathology, medicine.medical_specialty, Genetic Linkage, Endocrinology, Diabetes and Metabolism, Calvarium, Biology, Bone Morphogenetic Protein 1, Osteosclerosis, Endocrinology, Genetic linkage, medicine, Humans, Orthopedics and Sports Medicine, Craniofacial, Genetic Association Studies, Anatomy, medicine.disease, Pedigree, ADAM Proteins, Skull base, Skull, medicine.anatomical_structure, Dysplasia, Hyperostosis cranialis interna, Female, Human medicine, Amino Acid Oxidoreductases, Chromosome 8p21, Chromosomes, Human, Pair 8
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c526304e8b939de6f2ae1bf3202894fTest
https://doi.org/10.1007/s00223-013-9732-8Test -
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المؤلفون: Rik Hendrickx, R. Rooman, J. K. Van Camp, K. Van Hoorenbeeck, Guy Massa, L. Van Gaal, An Verrijken, Sigri Beckers, W. Van Hul, V. de Craemer, Doreen Zegers, Kristine Desager
المصدر: Pediatric Obesity. 9:36-42
مصطلحات موضوعية: medicine.medical_specialty, Mutation, Nutrition and Dietetics, business.industry, Health Policy, Point mutation, Public Health, Environmental and Occupational Health, Overweight, Bioinformatics, medicine.disease, medicine.disease_cause, Obesity, Phenotype, Childhood obesity, Endocrinology, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, Coding region, medicine.symptom, business, Gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::524243e5b918edaac4e7079c2be77605Test
https://doi.org/10.1111/j.2047-6310.2012.00131.xTest -
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المؤلفون: J. Gheuens, J. J. Martin, Michael Mullan, Gerd Multhaup, N.G. Irving, Antoon Vandenberghe, Hugh Gurling, W. Van Hul, A. Genthe, John Hardy, A. Wehnert, A. Barton, M. Salbaum, Bernhard Horsthemke, Marc Bruyland, H Backhovens, S. J. Richards, Konrad Beyreuther, C. Van Broeckhoven, A. Holland, Robert Williamson, Colin L. Masters, Peter Raeymaekers, Patrick Cras
المصدر: Nature
مصطلحات موضوعية: Adult, Male, Amyloid, Chromosomes, Human, Pair 21, Genetic Linkage, Locus (genetics), Disease, Biology, Alzheimer Disease, Genetic linkage, medicine, Humans, Senile plaques, Protein Precursors, Genetics, Amyloid beta-Peptides, Polymorphism, Genetic, Multidisciplinary, Molecular pathology, Chromosome Mapping, medicine.disease, Pedigree, Genes, Female, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73777dee0f802153a1b26c3c1a5967aTest
https://doi.org/10.1038/329153a0Test -
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المؤلفون: Tim Cundy, Nerea Alonso, Jennifer Walsh, Omar M. E. Albagha, Sachin Wani, M. Hooper, Stuart H. Ralston, W. Van Hul, Rogelio González-Sarmiento, M. Di Stefano, Geoffrey C. Nicholson, Alberto Falchetti, William D. Fraser, Micaela Rios Visconti, Kirsteen Goodman, G.C. Isaia, M. L. Brandi, JD Montes, Rosemary Dargie, Luigi Gennari, Socrates E. Papapoulos
المصدر: Osteoporosis International. 22:9-24
مصطلحات موضوعية: Genetics, medicine.diagnostic_test, business.industry, Endocrinology, Diabetes and Metabolism, Protein Data Bank (RCSB PDB), Single-nucleotide polymorphism, Genome-wide association study, medicine.disease, Genetic architecture, Paget's disease of bone, Attributable risk, medicine, Allele, business, Genetic testing
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e9d29d5a259f67c6971b0367b89435dfTest
https://doi.org/10.1007/s00198-011-1564-7Test