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Neuroendocrinology Letters, ISSN 0172-780X, 09/2018, Volume 39, Issue 3, pp. 149 - 155
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e46 - e53
Although the neurofibromatoses consist of at least three autosomal dominantly inherited disorders, neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2), and... 
GENOTYPE-PHENOTYPE CORRELATION | WHOLE-BODY MRI | FAMILIAL SCHWANNOMATOSIS | POSITRON-EMISSION-TOMOGRAPHY | VONRECKLINGHAUSEN NEUROFIBROMATOSIS | GENETIC-LINKAGE | PLEXIFORM NEUROFIBROMAS | ONCOLOGY | SHEATH TUMORS | TYPE-1 NF1 | MISMATCH REPAIR DEFICIENCY | Skin Neoplasms - diagnostic imaging | Skin Neoplasms - therapy | Central Nervous System Neoplasms - genetics | Humans | Neurilemmoma - diagnostic imaging | Neurofibromatosis 1 - diagnostic imaging | Optic Nerve Glioma - genetics | Central Nervous System Neoplasms - therapy | Infant | Optic Nerve Glioma - diagnostic imaging | Neurofibromatoses - genetics | Neurofibromatosis 1 - therapy | Optic Nerve Glioma - therapy | Magnetic Resonance Imaging | Neurilemmoma - therapy | Neurilemmoma - genetics | Central Nervous System Neoplasms - diagnostic imaging | Skin Neoplasms - genetics | Adolescent | Neurofibromatosis 1 - genetics | Child | Neurofibromatoses - diagnostic imaging | Neurofibromatoses - therapy | Pediatrics | Leukemia | Brain tumors | Central nervous system | Parents | Rhabdomyosarcoma | Neurofibromin 2 | Neurofibromatosis 2 | Cognition | Malignancy | Genetic screening | Risk factors | Osteoprotegerin | Children | Astrocytoma | Myelomonocytic leukemia | Organs | Health risks | Recklinghausen's disease | Morbidity | Hereditary diseases | Magnetic resonance imaging | Surveillance | Glioma | Neurofibromatosis | Diagnostic systems | Cancer | Tumors
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AJR. American journal of roentgenology, ISSN 0361-803X, 04/2019, Volume 212, Issue 4, pp. 892 - 898
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Neuroradiology, ISSN 0028-3940, 6/2019, Volume 61, Issue 6, pp. 711 - 720
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Journal Article
World Journal of Gastroenterology, ISSN 1007-9327, 01/2018, Volume 24, Issue 4, pp. 537 - 542
Journal Article