Results 31 to 40 of about 3,674 (207)

Primary retroperitoneal neurofibrosarcoma [PDF]

open access: yes, 2003
Malignant schwannoma or neurofibrosarcoma usually grows from the peripheral nerves and rarely from the retroperitoneum. When found in the retroperitoneum, it usually has a worse prognosis.
deOliveira, Michelle Lucinda   +1 more
core   +1 more source

Neurofibrome plexiforme cervical: à propos d’un cas

open access: yesThe Pan African Medical Journal, 2018
Le neurofibrome plexiforme est une tumeur bénigne rare des nerfs périphériques aux dépens des cellules conjonctives du périnevre. Il est pathognomonique de la neurofibromatose de type 1 (NF1 ou maladie de Von Recklinghausen).
Lamiae Bouimetarhan   +5 more
doaj   +1 more source

Aneurisma da artéria vertebral extracraniana em puérpera portadora de neurofibromatose clássica Extracranial vertebral artery aneurysm during the puerperium in women with neurofibromatosis type 1

open access: yesJornal Vascular Brasileiro, 2005
Paciente de 26 anos, no 10º dia de puerpério, apresentou dor súbita em região cervical esquerda irradiada para região supraclavicular do mesmo lado, seguida de aparecimento de massa pulsátil. Relatava hipertensão sistólica média de 160 mmHg, e diastólica
Carla Aparecida Faccio Bosnardo   +4 more
doaj   +1 more source

Neurofibromatose tipo 1: a propósito de um caso clínico [PDF]

open access: yes, 2013
A neurofibromatose é uma doença neurocutânea, genética, autossómica dominante. crónica e progressiva. Tem sido observada em todas as raças e em ambos os sexos.
Ascensão, Ana   +4 more
core  

Socially oriented attention in young children with neurofibromatosis type 1: An eye‐tracking study

open access: yesDevelopmental Medicine &Child Neurology, Volume 68, Issue 4, Page 541-548, April 2026.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.70050 Abstract Aim To examine visual engagement to social stimuli and response to joint attention in young children with neurofibromatosis type 1 (NF1) and typically developing peers (controls). Method Forty‐five preschool children were studied cross‐sectionally (mean age [SD] = 4 
Kristina M. Haebich   +6 more
wiley   +1 more source

Defektmissbildungen an den unteren Extremitäten [PDF]

open access: yes, 2018
Zusammenfassung: Missbildungen mit Defekten an den unteren Extremitäten sind selten. Sie entstehen in der Regel als toxische Schädigung während der Schwangerschaft zwischen der 4. und der 12.Woche. Es gibt auch solche mit hereditären Ursachen.
Hefti, F.
core  

Interventions supporting the empowerment of parent carers of children with neurodisability and other long‐term health conditions: A scoping review

open access: yesDevelopmental Medicine &Child Neurology, Volume 68, Issue 4, Page 489-500, April 2026.
This scoping review identified 145 different interventions designed to support parent carer empowerment. These interventions have been catalogued and are presented in an interactive, online database. Abstract Aim To compile information about interventions that have been developed to support the empowerment of parent carers of children and young people ...
Jim Reeder   +7 more
wiley   +1 more source

Neurofibromatose 1: à propos d'un cas historique

open access: yesThe Pan African Medical Journal, 2014
La neurofibromatose 1 (NF1) ou maladie de Von Recklinghausen est une maladie génétique fréquente. C'est une affection autosomique dominante qui se caractérise par une expression clinique variable au sein d'une même famille.
Nada El Moussaoui, Nadia Ismaili
doaj   +1 more source

Astrocitoma difuso das vias ópticas: Relato de caso

open access: yesBrazilian Neurosurgery, 2002
Os autores relatam o caso de uma paciente de 31 anos, portadora de neurofibromatose tipo I e astrocitoma pilocítico (confirmado por biopsia) que se estendia dos nervos ópticos à radiação geniculocalcarina bilateralmente.
Raul Starling Barros   +2 more
doaj   +1 more source

L'atteinte vésicale au cours de la neurofibromatose de Von Recklinghausen

open access: yesThe Pan African Medical Journal, 2014
La neurofibromatose de type 1 ou maladie de Von Recklinghausen est une maladie génétique autosomique dominante en rapport avec des mutations dans le gène suppresseur de tumeur NF1. L'atteinte uro-génitale au cours de cette maladie est rare et moins de 80
Mohamed Hicham Benazzouz   +6 more
doaj   +1 more source

Home - About - Disclaimer - Privacy