نتائج البحث - "Annemieke Boot"

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دورية أكاديمية

The international X-linked hypophosphataemia (XLH) registry (NCT03193476): rationale for and description of an international, observational study

المؤلفون: Raja Padidela, Ola Nilsson, Outi Makitie, Signe Beck-Nielsen, Gema Ariceta, Dirk Schnabel, Maria Luisa Brandi, Annemieke Boot, Elena Levtchenko, Michael Smyth, Ravi Jandhyala, Zulf Mughal

المصدر: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)

مصطلحات موضوعية: X-linked hypophosphataemia (XLH), Rare disease, Patient registry, Vitamin D, Disease history, Post-authorisation safety, Medicine

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s13023-020-01434-4; https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/d1eaabf96b4c4fabb33c9762c45a5fee

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دورية أكاديمية

Development of an observational registry for genetic hypophosphatemia and acquired renal phosphate wasting in The Netherlands: ORPHOS-NED

المؤلفون: Ariadne Bosman, Natasha Appelman-Dijkstra, Joop van den Bergh, Arend Bökenkamp, Annemieke Boot, Martin de Borst, Bram van der Eerden, M. Carola Zillikens

المصدر: Bone Reports, Vol 14, Iss , Pp 101003- (2021)

مصطلحات موضوعية: Diseases of the musculoskeletal system, RC925-935

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2352187221002588; https://doaj.org/toc/2352-1872

URL الوصول: https://doaj.org/article/c954f250efc54771ada0178822d60670

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The international X-linked hypophosphataemia (XLH) registry (NCT03193476) : rationale for and description of an international, observational study

المؤلفون: Ola Nilsson, Zulf Mughal, Outi Mäkitie, Maria Luisa Brandi, Michael Smyth, Dirk Schnabel, Annemieke Boot, Ravi Jandhyala, Raja Padidela, Signe Sparre Beck-Nielsen, Gema Ariceta, Elena Levtchenko

المساهمون: HUS Children and Adolescents, Clinicum, Lastentautien yksikkö, Children's Hospital, University of Helsinki, Helsinki University Hospital Area

المصدر: Padidela, R, Nilsson, O, Makitie, O, Beck-Nielsen, S, Ariceta, G, Schnabel, D, Brandi, M L, Boot, A, Levtchenko, E, Smyth, M, Jandhyala, R & Mughal, Z 2020, ' The international X-linked hypophosphataemia (XLH) registry (NCT03193476) : rationale for and description of an international, observational study ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, 172 . https://doi.org/10.1186/s13023-020-01434-4
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Orphanet Journal of Rare Diseases

مصطلحات موضوعية: Adult, 0301 basic medicine, Quality of life, Pediatrics, medicine.medical_specialty, X-linked hypophosphataemia (XLH), lcsh:Medicine, 030209 endocrinology & metabolism, Rickets, Disease, Disease history, Phosphates, 03 medical and health sciences, 0302 clinical medicine, Humans, Medicine, Pharmacology (medical), Registries, Family history, Vitamin D, Child, Wasting, Genetics (clinical), Bone growth, Real-world evidence, XLH management, Osteomalacia, Bburosumab, business.industry, Research, lcsh:R, 1184 Genetics, developmental biology, physiology, General Medicine, medicine.disease, 3. Good health, PREVALENCE, Fibroblast Growth Factor-23, 030104 developmental biology, Patient registry, Familial Hypophosphatemic Rickets, medicine.symptom, business, Rare disease, Post-authorisation safety

وصف الملف: application/pdf; Electronic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee5cd7b55197d8ecd9ed307db6be743
http://hdl.handle.net/10138/318409

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Sustained efficacy and safety of burosumab, a fully human anti-FGF23 monoclonal antibody, in children and early adolescents with X-linked hypophosphatemia

المؤلفون: Wolfgang Hogler, Thomas Carpenter, Erik Imel, Anthony Portale, Annemieke Boot, Agnes Linglart, Raja Padidela, William van't Hoff, Meng Mao, Alison Skrinar, Javier San Martin, Michael Whyte

المصدر: Bone Abstracts.

مصطلحات موضوعية: business.industry, medicine.drug_class, Immunology, Early adolescents, Medicine, General Medicine, business, Monoclonal antibody, X-linked hypophosphatemia, medicine.disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::560dfbe94ee20f19fcf5eaced92baf0e
https://doi.org/10.1530/boneabs.7.oc15

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Automated radiogrammetry is a feasible method for measuring bone quality and bone maturation in severely disabled children

المؤلفون: Heleen M. Evenhuis, Stella A. de Man, Wim A. R. Huijbers, Annemieke Boot, Rick R. van Rijn, Karen Bindels-de Heus, Sandra Mergler, Corine Penning

المساهمون: Other Research, Radiology and Nuclear Medicine, General Practice, Pediatrics

المصدر: Pediatric radiology, 46(7), 1017-1022. Springer Verlag
Pediatric Radiology, 46(7), 1017-1022. Springer-Verlag
Pediatric radiology, 46(7), 1017-1022. SPRINGER
Pediatric Radiology

مصطلحات موضوعية: Male, Bone density, SEVERE CEREBRAL-PALSY, 030218 nuclear medicine & medical imaging, 0302 clinical medicine, Bone Density, Intellectual disability, Child, Children, Netherlands, Bone age, X-RAY ABSORPTIOMETRY, Disabled Children, Hand Bones, Radiology Nuclear Medicine and imaging, Radiographic Image Interpretation, Computer-Assisted, GROWTH, Female, Original Article, HEALTH, Hand bones, medicine.medical_specialty, Bone quality, Bone development, Bone maturation, Automated radiogrammetry, macromolecular substances, 03 medical and health sciences, FRACTURES, Age Determination by Skeleton, medicine, Humans, Radiology, Nuclear Medicine and imaging, Pediatrics, Perinatology, and Child Health, Bone Development, Disability, business.industry, GROSS MOTOR FUNCTION, ADULTS, medicine.disease, Radiography, SKELETAL MATURATION, Cross-Sectional Studies, Pediatrics, Perinatology and Child Health, Physical therapy, Feasibility Studies, MODERATE, MINERAL DENSITY, business, Neurological impairment, Software, 030217 neurology & neurosurgery