Results 131 to 140 of about 1,890 (196)

Deep learning for dual detection of microsatellite instability and POLE mutations in colorectal cancer histopathology. [PDF]

NPJ Precis Oncol
Gustav M, Reitsam NG, Carrero ZI, Loeffler CML, van Treeck M, Yuan T, West NP, Quirke P, Brinker TJ, Brenner H, Favre L, Märkl B, Stenzinger A, Brobeil A, Hoffmeister M, Calderaro J, Pujals A, Kather JN.   +17 more
europepmc   +1 more source

Laparoscopic-assisted Resection of a Retroperitoneal Lumbar Nerve Root Neurofibroma: A Case Report. [PDF]

Rev Bras Ortop (Sao Paulo)
Relvas-Silva M, Lima ER, Silva MR, Neves N.   +3 more
europepmc   +1 more source

Lung cancer and parenchymal lung disease in a patient with neurofibromatosis type 1. [PDF]

J Bras Pneumol, 2019
Melo ASA, Alves SF, Antunes PM, Zanetti G, Marchiori E.   +4 more
europepmc   +1 more source

Discrimination of benign, atypical, and malignant peripheral nerve sheath tumors in neurofibromatosis type 1 using diffusion-weighted MRI. [PDF]

Neurooncol Adv
Ristow I, Kaul MG, Stark M, Zapf A, Zapf A, Riedel C, Lenz A, Mautner VF, Farschtschi S, Apostolova I, Adam G, Bannas P, Salamon J, Well L.   +13 more
europepmc   +1 more source

Van Abbahit tot Zweedse coalitie. Recente waarnemingen van de Scandinavische wereld in woord en verwijzing. [PDF]

, 2016
De Grauwe, Luc
core   +1 more source

Portuguese Pancreatic Club Perspectives on Pancreatic Neuroendocrine Neoplasms: Diagnosis and Staging, Associated Genetic Syndromes and Particularities of Their Clinical Approach. [PDF]

GE Port J Gastroenterol
Ferreira-Silva J, Meireles S, Falconi M, Fernandes A, Vilas-Boas F, Bispo M, Rio-Tinto R, Rodrigues-Pinto E, Portuguese Pancreatic Club, specialized section of the Portuguese Society of Gastroenterology.   +9 more
europepmc   +1 more source

Atteinte pulmonaire sévère au cours de la neurofibromatose de type 1 [PDF]

Revue des Maladies Respiratoires, 2014
Type 1 neurofibromatosis (NF1) is a hereditary disease inherited as an autosomal dominant. Respiratory involvement is rare. We report the case of a woman suffering from NF1 with mutation of the corresponding gene and with respiratory involvement combining diffuse parenchymatous lesions, severe precapillary pulmonary hypertension and an enlarging ...
Martignac, B., Gagnadoux, Frédéric, Trzepizur, Wojciech, Beneton, Nathalie, Vinchon, F., Paris, Audrey, Montani, D., Goupil, François   +7 more
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Neurofibromatose de type 1

La Presse Médicale, 2006
Neurofibromatosis type 1 (NF1) is often associated with psychiatric disorders, which are more frequent in NF1 than in general population (33% of patients). Dysthymia is the most frequent diagnosis (21% of patients). There is also a high prevalence of depressive mood (7%), anxiety (1-6%), and personality (3%) disorders. The risk of suicide is four times
Raoul Belzeaux, Christophe Lançon
openaire   +1 more source

Imagerie de la neurofibromatose de type 1

Feuillets de Radiologie, 2016
Resume La neurofibromatose de type 1 est la plus frequente des phacomatoses et des neurofibromatoses, avec une incidence de 1/2500 naissances. Transmise sur le mode autosomique dominant, elle se traduit par la presence de tumeurs principalement cutanees, cerebrales et des nerfs peripheriques, et par des dysplasies osseuses et vasculaires. Les lesions
M. Koob, J.-L. Dietemann
openaire   +1 more source