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المصدر: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Orphanet Journal of Rare Diseasesمصطلحات موضوعية: Adult, Male, Craniofacial alteration, medicine.medical_specialty, Neurofibromatosis 1, Adolescent, Mandibular canal, Periapical cemental dysplasia, lcsh:Medicine, Review, Young Adult, 03 medical and health sciences, 0302 clinical medicine, medicine, Speech, Humans, Pharmacology (medical), In patient, Oral soft tissue, Tooth Developoment, Neurofibromatosis, Craniofacial, Child, Periapical Cemental dysplasia, Genetics (clinical), Aged, Dental age, business.industry, Periapical Diseases, Skull, lcsh:R, Mandible, Wide Mandibular Canal, 030206 dentistry, General Medicine, Middle Aged, University hospital, medicine.disease, Dermatology, medicine.anatomical_structure, Female, Abnormality, Mouth Diseases, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f9de14b95de6f8b77e0f8dbdc052cf0Test
http://link.springer.com/article/10.1186/s13023-018-0881-8Test -
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المؤلفون: Roberto Eleopra, Alessandro Moro, Sara Rinaldo, Daniela Macor, Christian Lettieri, Michele De Filippo, Grazia Devigili, Andrea Dardis, Bruno Bembi, Giovanni Ciana
المصدر: Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-10 (2017)
Orphanet Journal of Rare Diseasesمصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Adolescent, Peripheral neuropathy, lcsh:Medicine, Neuropathic pain, Young Adult, 03 medical and health sciences, Bone pain, 0302 clinical medicine, Surveys and Questionnaires, Humans, Medicine, Pharmacology (medical), Child, Genetics (clinical), Skin, Small fibre neuropathy, Gaucher Disease, business.industry, Research, lcsh:R, Chronic pain, General Medicine, Enzyme replacement therapy, Hypoesthesia, Middle Aged, medicine.disease, Dermatology, Cross-Sectional Studies, 030104 developmental biology, Child, Preschool, Pain Origin, Hyperalgesia, Gaucher type 1 disease, Neuralgia, Female, Chronic Pain, medicine.symptom, business, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::859d05fc711f44fee13f4459c4a2e5f4Test
http://link.springer.com/article/10.1186/s13023-017-0700-7Test -
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المؤلفون: Machi Suka, Chikako Nishigori, Takashi Yamauchi, Hiroyuki Yanagisawa
المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-7 (2019)مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Neurofibromatosis 1, Adolescent, Databases, Factual, lcsh:Medicine, 030105 genetics & heredity, 03 medical and health sciences, Young Adult, Intractable rare disease, 0302 clinical medicine, Quality research, Japan, Medicine, Humans, Pharmacology (medical), In patient, Registries, Neurofibromatosis, Stage (cooking), Child, Genetics (clinical), Progression, business.industry, Incidence (epidemiology), Research, Incidence, Follow-up, lcsh:R, Disease progression, Infant, Newborn, Infant, Subsidy, General Medicine, Middle Aged, medicine.disease, National registry, Medical expense subsidies, Child, Preschool, Disease Progression, Female, business, 030217 neurology & neurosurgery, Neurofibromatosis type 1
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84ba4e4498d35e6c24fee0ccaeca8bcbTest
https://hdl.handle.net/20.500.14094/90006223Test