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Key features of neurofibromatoses 1 and 2
Archives of disease in childhood - Education & practice edition, 2012The neurofibromatoses are a group of relatively common autosomal dominant disorders that have a broad spectrum of clinical manifestations. While most clinicians are familiar with the key features of neurofibromatosis 1 (NF1), many of the …
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Symptomatische tumoren bij neurofibromatose type 1
Nederlands Tijdschrift voor Geneeskunde, 2023Neurofibromatosis type 1 (NF1) is a hereditary, progressive and unpredictable disease, which can involve many organs. Benign and malignant tumors arise due to unrestrained cell division and cell growth. Recognizing the symptoms of these tumors and using the correct diagnostics is of great importance.
Taal, Walter +5 more
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Wirbelsäulendeformitäten bei Neurofibromatose Typ 1
Der Orthopäde, 2021Christoph-E. Heyde +4 more
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The Neurofibromatoses. Part 1: NF1.
Reviews in neurological diseases, 2009The neurofibromatoses, including neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2), and schwannomatosis, comprise a group of genetically distinct disorders of the nervous system unified by the predisposition to nerve sheath tumors. NF1 is the most common neurogenetic disorder, with a birth incidence of 1 in 3000.
Christine, Lu-Emerson, Scott R, Plotkin
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Neurofibrosarkome bei Neurofibromatose 1
DMW - Deutsche Medizinische Wochenschrift, 2008J. P. Sieb, H. Mattle, M. Pirovino
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