Results 71 to 80 of about 3,674 (207)
Forma central da moléstia nervosa de Recklinghausen
Arquivos de Neuro-Psiquiatria, 1958 Os autores apresentam uma sistematização das lesões que podem ser encontradas na moléstia de Recklinghausen. Foram observados 4 casos de forma nervosa central da moléstia.
L. C. Mattosinho França +1 more
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Klinisch-zeitlicher Verlauf eines solitären retinalen Astrozytoms [PDF]
, 2018 Zusammenfassung: Retinale Astrozytome sind benigne Tumoren der Netzhaut. Ihr Auftreten kann solitär oder multipel, selten auch bilateral oder als teil eines Syndroms (tuberöse Sklerose, Neurofibromatose Typ I) sein.
Duncker, G.I.W. +3 more
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Muscle action potential scans and ultrasound imaging in neurofibromatosis type 2 [PDF]
, 2016 INTRODUCTION: The neuropathy in patients with neurofibromatosis type 2 (NF2) is difficult to quantify and follow up. In this study we compared 3 methods that may help assess motor axon pathology in NF2 patients.
Bostock, H +5 more
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Nodules de lisch dans la neurofibromatose type 1
The Pan African Medical Journal, 2017 La neurofibromatose 1 (NF1) ou maladie de Von Recklinghausen est une maladie qui se manifeste par des taches café au lait cutanées et des neurofi bromes. C'est une des maladies génétiques les plus fréquentes à transmission autosomique dominant.
Yassine Abaloun, Yousra Ajhoun
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Abordagem cirúrgica de neurofibroma gigante Surgical correction of a giant neurofibroma
Revista Brasileira de Cirurgia Plástica, 2012 Neurofibromatose é uma doença de origem genética autossômica dominante composta por três tipos: neurofibromatose tipo 1 (NF1), neurofibromatose tipo 2 (NF2) e schwannomatose.
Iana Silva Dias +4 more
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Mundschleimhaut als Spiegel systemischer Erkrankungen [PDF]
, 2018 Zusammenfassung: Viele Systemerkrankungen können sich an der Mundschleimhaut als zielführender "Nebenbefund" zeigen und mitunter auf eine noch latente Grunderkrankung hinweisen.
Fistarol, S.K., Itin, P.H.
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Please Download the Front Cover Page Here
Health Research in AfricaIllustrations of the cover page from top down 2.
Samuel Nko'o Amvene
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The Pan African Medical Journal, 2014 La neurofibromatose de type 1 (NF1) ou maladie de Recklinghausen est une génodermatose autosomique dominante, elle touche de 1/3000 à 1/4000 personnes. La NF1 est caractérisée par une variabilité de son expression clinique qu'on peut retrouver au sein de
Kbira El Morabite, Baderddine Hassam
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Múltiplos defeitos localizados da camada de fibras nervosas em um paciente com glioma de nervo óptico no olho contralateral: relato de caso [PDF]
, 2009 This case report describes a young non-glaucomatous patient with neurofibromatosis and previous history of optic nerve glioma, which developed multiple wedge-shaped retinal nerve fiber layer defects close to a chorioretinal scar in the fellow eye.
Lima, Verônica Castro +4 more
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Multiple endocrine neoplasia [PDF]
, 2007 The knowledge of genetics has increased in recent years and has led to important changes in management of hereditary diseases. Multiple endocrine neoplasia is characterized by the occurrence of benign or malign tumours involving two or more endocrine ...
Guimarães, J
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