Results 71 to 80 of about 3,743 (226)
FEOCROMOCITOMA E NEUROFIBROMATOSE 1
Introdução: Feocromocitomas são tumores originários de células cromafins do sistema simpato-adrenal. As suas manifestações clínicas são múltiplas e diversificadas, função do perfil secretório variável de múltiplos compostos, incluindo catecolaminas ...
Rui Tavares-Bello +5 more
doaj +1 more source
Neurofibromatose Tipo 1: Envolvimento Cutâneo Exuberante
N/a.
Sandra Ferreira +2 more
doaj +1 more source
Comparação entre tomografia computadorizada e ressonância magnética nos esclarecimento etiológico de epilepsias parciais. [PDF]
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Alcantara, Karla de Bem
core
Neurofibromatosis: part 2 – clinical management
Part 1 of this guideline addressed the differential diagnosis of the neurofibromatoses (NF): neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SCH). NF shares some features such as the genetic origin of the neural tumors
Pollyanna Barros Batista +27 more
doaj +1 more source
Multiple endocrine neoplasia [PDF]
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
core
Avaliação do stress parental em mães de crianças com perturbação de hiperatividade com défice de atenção [PDF]
Introdução: Pretendeu-se identificar os níveis de stress nas mães de crianças e adolescentes com perturbação de hiperatividadecom défice de atenção e verificar se existe uma associação entre o stress percecionado por estas mães e o funcionamento familiar.
Almeida, P. +5 more
core +1 more source
Abstract Background Cutaneous neurofibromas (cNFs) are a major cause of disfigurement in patients with Neurofibromatosis Type 1 (NF1). However, clinical trials investigating cNF treatments lack standardised outcome measures to objectively evaluate changes in cNF size and appearance.
Jonathan C. L. Lau +12 more
wiley +1 more source
Hyperthyroidism related to McCune-Albright syndrome: report of two cases and review of the literature [PDF]
INTRODUCTION: McCune-Albright syndrome is a sporadic disease clinicaly characterized by polyostotic fibrous dysplasia, café-au-lait cutaneous spots and hyperfunctional endocrinopathies, such as precocious puberty, hyperthyroidism, acromegaly and others ...
Abs R +51 more
core +3 more sources
Neurofibromatoses: part 1 ? diagnosis and differential diagnosis
Neurofibromatoses (NF) are a group of genetic multiple tumor growing predisposition diseases: neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2) and schwannomatosis (SCH), which have in common the neural origin of tumors and cutaneous signs ...
Luiz Oswaldo Carneiro Rodrigues +24 more
doaj +1 more source
Abstract Background and Purpose Thalamic hypometabolism is a consistent finding in brain PET with F‐18 fluorodeoxyglucose (FDG) in patients with neurofibromatosis type 1 (NF1). However, the pathophysiology of this metabolic alteration is unknown. We hypothesized that it might be secondary to disturbance of peripheral input to the thalamus by NF1 ...
Cansu Özden +10 more
wiley +1 more source

