Results 131 to 140 of about 553 (178)
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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
Neurofibromatose de type 1 et formes variantes
Annales De Dermatologie Et De Vénéréologie, FMC, 2022P Combemale, S Pinson
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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Nodules de Lisch dans la neurofibromatose de type 1
Journal Francais D'Ophtalmologie, 2020Leila Knani, Ahmed Mahjoub, H Mahjoub
exaly

