Results 161 to 170 of about 3,743 (226)

Intramedullary ependymoma: a revision of the literature following diagnosis of a clinical case [PDF]

, 2009
Batista, R, Fonseca, I, Pina, R, Saldanha, MH   +3 more
core  

Experiences of stigmatization and its impacts among individuals living with hereditary diseases and family members in Portugal: an exploratory study. [PDF]

J Community Genet
Valentim J, Paneque M, Mendes Á.
europepmc   +1 more source

[Precocious puberty in the McCune-Albright Syndrome: a case report]. [PDF]

Pan Afr Med J
Rifai K, El Moatamid K, Iraqi H, Talbi D, Gharbi MEH.   +4 more
europepmc   +1 more source

Burden of adult neurofibromatosis 1: development and validation of a burden assessment tool. [PDF]

Orphanet J Rare Dis, 2019
Armand ML, Taieb C, Bourgeois A, Bourlier M, Bennani M, Bodemer C, Wolkenstein P, along with the French national network on rare skin diseases (FIMARAD).   +7 more
europepmc   +1 more source

Tumores do Estroma Gastrointestinal (GISTs), a propósito de um Caso Clínico [PDF]

, 2013
Joana Filipa da Silva Bouça
core  

Development of a semi-automatic segmentation technique based on mean magnetic resonance imaging intensity thresholding for volumetric quantification of plexiform neurofibromas. [PDF]

Heliyon
Kiaei DS, El-Jalbout R, Décarie JC, Perreault S, Dehaes M.   +4 more
europepmc   +1 more source

Problèmes d'apprentissage scolaire et neurofibromatose 1

Glossa, 1996
Jacques Zeller, Pierre Wolkenstein
doaj  

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Neurofibromatoses

Hematology/Oncology Clinics of North America, 2022
The neurofibromatoses are a group of genetic disorders that cause development of nervous system tumors as well as various other tumor and systemic manifestations. Neurofibromatosis type 1 is the most prevalent of these conditions and has the most variable phenotype and highest risk of malignant tumor formation.
Justin T, Jordan, Scott R, Plotkin
openaire   +2 more sources

Neurofibromatose

Neurologie up2date, 2022
Die Symptome einer Neurofibromatose können in allen Altersklassen erstmals auftreten, häufig bereits in den ersten 3 Lebensdekaden, teilweise mit sehr langsamer Entwicklung über Jahrzehnte oder rasch progredient innerhalb weniger Monate. Unter anderem diese unterschiedliche
Cordula Matthies, Eva Rampeltshammer, Maria Breun   +2 more
openaire   +1 more source

Neurofibromatoses

2012
The studies of familial tumor predisposition syndromes have contributed immensely to our understanding of oncogenesis. Neurofibromatosis 1, neurofibromatosis 2 and schwannomatosis are inherited autosomal dominant neurocutaneous disorders with complete penetrance.
Erik J, Uhlmann, Scott R, Plotkin
openaire   +3 more sources