Results 161 to 170 of about 971 (198)
Some of the next articles are maybe not open access.
2016
Portuguese Journal of Pediatrics, Vol. 47 No. 4 (2016)
Rebelo, Alícia +2 more
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Portuguese Journal of Pediatrics, Vol. 47 No. 4 (2016)
Rebelo, Alícia +2 more
openaire +2 more sources
Der Radiologe, 2013
Neurofibromatosis type 1 (NF1) and type 2 (NF2) are hereditary autosomal dominant neurocutaneous disorders, the phacomatoses, characterized by the development of tumors derived from the cells of the peripheral nerve sheath and also includes schwannomatosis.
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Neurofibromatosis type 1 (NF1) and type 2 (NF2) are hereditary autosomal dominant neurocutaneous disorders, the phacomatoses, characterized by the development of tumors derived from the cells of the peripheral nerve sheath and also includes schwannomatosis.
openaire +2 more sources
Postgraduate Medicine, 1988
These are exciting times for patients and physicians concerned with the neurofibromatoses. These disorders have been known to medicine for more than 100 years, and now there is hope of achieving a thorough understanding of their pathogenesis. Despite this optimism, the need for careful clinical management of these patients and for solid clinical ...
openaire +2 more sources
These are exciting times for patients and physicians concerned with the neurofibromatoses. These disorders have been known to medicine for more than 100 years, and now there is hope of achieving a thorough understanding of their pathogenesis. Despite this optimism, the need for careful clinical management of these patients and for solid clinical ...
openaire +2 more sources
Management of neurofibromatosis type 1-associated plexiform neurofibromas
Neuro-Oncology, 2022Kaleb Yohay +2 more
exaly
Skeletveränderungen bei Neurofibromatose
1968Die Neurofibromatose ist eine Erbkrankheit (Abb. 1). Der Erbgang ist meistens strikte autosomal dominant, seltener unregelmasig dominant, selten recessiv. Hoekstea (1922) hat 63 Stammbaume aus der Literatur gesammelt. Eine Ubersicht uber die genetischen Aspekte findet sich bei Gates (1946).
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Neurofibrosarcoma at irradiation site in a patient with neurofibromatosis and wilms' tumor
Ca-A Cancer Journal for Clinicians, 1981Jen-Yih Chu, Dennis M O'Connor
exaly
Author's reply: Wilms' tumor and neurofibromatosis
Ca-A Cancer Journal for Clinicians, 1982Giulio J D'Angio, G J D'Angio
exaly