Lista de obras - Manuel Melo Pires - Dominio Público Uruguay

A novel molecular link between HOXA9 and WNT6 in glioblastoma identifies a subgroup of patients with particular poor prognosis

scientific article published on 10 January 2020

A retrospective study of Creutzfeldt-Jakob disease in North of Portugal 1993-2002: demographic, clinical and neuropathological features

artículo científico publicado en 2003

Benign osteoblastoma of the sphenoid bone.

artículo científico publicado en 2009

Biopsy experience in a FAP endemic area.

artículo científico publicado en 2015

CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings

artículo científico publicado en 2014

Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): postmortem findings

artículo científico publicado en 2015

Computed tomographic findings of brain and skull in myotonic dystrophy

artículo científico publicado en 1987

Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer's Disease Clinical Phenotypes? A Clinico-Pathological Perspective

artículo científico publicado en 2016

Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene

artículo científico publicado en 2017

Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database.

artículo científico publicado en 2012

Frontotemporal lobar degeneration-TDP with 'multiple system atrophy phenocopy syndrome'.

artículo científico publicado en 2017

Hansen Neuropathy: Still a Possible Diagnosis in the Investigation of a Peripheral Neuropathy.

artículo científico

Impact of EGFR genetic variants on glioma risk and patient outcome.

artículo científico publicado en 2011

Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review.

artículo científico publicado en 2017

L-2-Hydroxyglutaric aciduria: clinical, biochemical and magnetic resonance imaging in six Portuguese pediatric patients.

artículo científico publicado en 1997

Loss of WNK2 expression by promoter gene methylation occurs in adult gliomas and triggers Rac1-mediated tumour cell invasiveness

artículo científico publicado en 2012

Medulloblastoma and gliomatosis cerebri: rare brain tumors in multiple sclerosis patients.

artículo científico publicado en 2011

Monocarboxylate transporters (MCTs) in gliomas: expression and exploitation as therapeutic targets

artículo científico publicado en 2012

New massive parallel sequencing approach improves the genetic characterization of congenital myopathies

artículo científico publicado en 2016

New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing

artículo científico publicado en 2015

Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency

artículo científico publicado en 2013

Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration

artículo científico publicado en 2017

The etiology of spontaneous intracerebralhemorrhage: Insights from a neuropathological series.

artículo científico publicado en 2017

Usher syndrome and Nebulin-associated myopathy in a single patient due to variants in <i>MYO7A</i> and <i>NEB</i>

artículo científico publicado en 2020

[Multiple paraneoplastic syndromes occurring in the same patient: clinical, imaging and neuro-pathological documentation]

artículo científico publicado en 2006

Lista de obras de Manuel Melo Pires

A novel molecular link between HOXA9 and WNT6 in glioblastoma identifies a subgroup of patients with particular poor prognosis

A retrospective study of Creutzfeldt-Jakob disease in North of Portugal 1993-2002: demographic, clinical and neuropathological features

Benign osteoblastoma of the sphenoid bone.

Biopsy experience in a FAP endemic area.

CNS involvement in V30M transthyretin amyloidosis: clinical, neuropathological and biochemical findings

Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): postmortem findings

Computed tomographic findings of brain and skull in myotonic dystrophy

Does the Interplay Between Aging and Neuroinflammation Modulate Alzheimer's Disease Clinical Phenotypes? A Clinico-Pathological Perspective

Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene

Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database.

Frontotemporal lobar degeneration-TDP with 'multiple system atrophy phenocopy syndrome'.

Hansen Neuropathy: Still a Possible Diagnosis in the Investigation of a Peripheral Neuropathy.

Impact of EGFR genetic variants on glioma risk and patient outcome.

Inflammatory myopathy associated with myasthenia gravis with and without thymic pathology: Report of four cases and literature review.

L-2-Hydroxyglutaric aciduria: clinical, biochemical and magnetic resonance imaging in six Portuguese pediatric patients.

Loss of WNK2 expression by promoter gene methylation occurs in adult gliomas and triggers Rac1-mediated tumour cell invasiveness

Medulloblastoma and gliomatosis cerebri: rare brain tumors in multiple sclerosis patients.

Monocarboxylate transporters (MCTs) in gliomas: expression and exploitation as therapeutic targets

New massive parallel sequencing approach improves the genetic characterization of congenital myopathies

New splicing mutation in the choline kinase beta (CHKB) gene causing a muscular dystrophy detected by whole-exome sequencing

Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency

Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration

The etiology of spontaneous intracerebralhemorrhage: Insights from a neuropathological series.

Usher syndrome and Nebulin-associated myopathy in a single patient due to variants in <i>MYO7A</i> and <i>NEB</i>

[Multiple paraneoplastic syndromes occurring in the same patient: clinical, imaging and neuro-pathological documentation]

is a novel oncogenic prognostic biomarker in human glioblastoma