Estudios neuropatológicos post-mortem en el caso del SIDA.

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Hippocampal pathology in progressive supranuclear palsy (PSP): a quantitative study of 8 cases.

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A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt-Jakob disease (vCJD).

Neuropathology and applied neurobiology·2009

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Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases.

Journal of neural transmission (Vienna, Austria : 1996)·2007

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Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene.

Journal of neurology, neurosurgery, and psychiatry·2007

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Adult cerebellar liponeurocytoma with predominant pilocytic pattern and myoid differentiation.

Neuropathology and applied neurobiology·2007

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Multiple system atrophy (MSA): topographic distribution of the alpha-synuclein-associated pathological changes.

Parkinsonism & related disorders·2006

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Assisted dying and the silencing of medicine's next generation.

Lancet (London, England)·2026

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Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Lancet (London, England)·2026

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Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

Lancet (London, England)·2026

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[<sup>177</sup>Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.

Lancet (London, England)·2026

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Research priorities for characterising Bundibugyo virus.

Lancet (London, England)·2026

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Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.

Lancet (London, England)·2026

Videos de Experimentos Relacionados

Estudios neuropatológicos post-mortem en el caso del SIDA.

Videos de Conceptos Relacionados

Hippocampal pathology in progressive supranuclear palsy (PSP): a quantitative study of 8 cases.

A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt-Jakob disease (vCJD).

Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases.

Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene.

Adult cerebellar liponeurocytoma with predominant pilocytic pattern and myoid differentiation.

Multiple system atrophy (MSA): topographic distribution of the alpha-synuclein-associated pathological changes.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

[<sup>177</sup>Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.

Research priorities for characterising Bundibugyo virus.

Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.

Videos de Experimentos Relacionados

Estudios neuropatológicos post-mortem en el caso del SIDA.

Videos de Conceptos Relacionados

Artículos Relacionados

Hippocampal pathology in progressive supranuclear palsy (PSP): a quantitative study of 8 cases.

A quantitative study of the pathological changes in the cerebellum in 15 cases of variant Creutzfeldt-Jakob disease (vCJD).

Progressive supranuclear palsy (PSP): a quantitative study of the pathological changes in cortical and subcortical regions of eight cases.

Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene.

Adult cerebellar liponeurocytoma with predominant pilocytic pattern and myoid differentiation.

Multiple system atrophy (MSA): topographic distribution of the alpha-synuclein-associated pathological changes.

Assisted dying and the silencing of medicine's next generation.

Linguistic pragmatism: a woman with progressive abdominal pain in Thailand.

Medical compartmentalisation: a patient with chromosome 22q11.2 deletion syndrome in Japan.

[<sup>177</sup>Lu]Lu-edotreotide versus everolimus for gastroenteropancreatic neuroendocrine tumours (COMPETE): a phase 3, multicentre, randomised, open-label, superiority trial.

Research priorities for characterising Bundibugyo virus.

Rethinking treatment sequence in advanced gastroenteropancreatic neuroendocrine tumours.