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- Gliomas - Symptoms, diagnosis and treatment | BMJ Best Practice
IDH-wildtype diffuse glioma (glioblastoma) is an aggressive primary brain tumour that presents in patients in the sixth or seventh decade of life IDH-mutant gliomas (including oligodendroglioma, IDH-mutant, 1p 19q codeleted, grades 2-3; and astrocytoma, IDH-mutant, grades 2-4) tend to occur in young or middle-age patients
- Gliomas - Sintomas, diagnóstico e tratamento | BMJ Best Practice
O glioma difuso de tipo selvagem da IDH (glioblastoma) é um tumor cerebral primário agressivo que se apresenta em pacientes na sexta ou sétima décadas de vida Gliomas com mutações em IDH (tais como oligodendroglioma, com mutação em IDH e codeleção de 1p 19q, graus 2-3; e astrocitoma, com mutação em IDH, graus 2-4) tendem a ocorrer
- Symptoms, diagnosis and treatment - BMJ Best Practice
Tumour lysis syndrome (TLS) is an oncological emergency caused by rapid breakdown of cancer cells and subsequent release of large amounts of intracellular content into the bloodstream
- Long QT syndrome - Symptoms, diagnosis and treatment - BMJ Best Practice
Long QT syndrome (LQTS) is a congenital or acquired condition that is characterised by a prolonged QT interval on the surface ECG and is associated with a high risk of sudden cardiac death due to ventricular tachyarrhythmias
- Symptoms, diagnosis and treatment - BMJ Best Practice US
Meningioma is a predominantly nonmalignant tumor of the meninges occurring at both cranial and spinal sites Can be asymptomatic or cause symptoms from local mass effect due to compression of neural structur
- Neurofibromatose do tipo 1 - BMJ Best Practice
A neurofibromatose do tipo 1 (NF1) é um distúrbio genético autossômico dominante definida pelas características de manchas café-com-leite, múltiplos neurofibromas e nódulos de Lisch na íris
- Symptoms, diagnosis and treatment - BMJ Best Practice
Type 1 neurofibromatosis (NF1) is an autosomal-dominant genetic disorder with the defining features of café au lait spots, multiple neurofibromas, and iris Lisch nodules
- Symptoms, diagnosis and treatment - BMJ Best Practice
Tuberous sclerosis complex is an autosomal-dominant, neurocutaneous, multi-system disorder characterised by cellular hyperplasia, tissue dysplasia, and multiple organ hamartomas
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