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List of works by Manuel Melo Pires

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

scientific article

Benign osteoblastoma of the sphenoid bone.

scientific article published on November 2009

Biopsy experience in a FAP endemic area.

scientific article published on 2 November 2015

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

scientific article published on 4 August 2014

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

scientific article published in February 2015

Computed tomographic findings of brain and skull in myotonic dystrophy

scientific article published on 01 October 1987

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

scientific article published on 11 May 2016

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

scientific article published on 3 October 2017

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

scientific article published on 12 September 2012

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

scientific article

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

scientific article published on May 2015

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

scientific article

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

scientific article

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

scientific article published in June 1997

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

scientific article

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

scientific article

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

scientific article published on 20 December 2012

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

scientific article published on 4 February 2016

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

scientific article published on 5 March 2015

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

scientific article published on 28 March 2013

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

scientific article

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

scientific article published on 20 November 2017

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

scientific article published on 30 July 2020

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

scientific article published on 01 November 2006

is a novel oncogenic prognostic biomarker in human glioblastoma

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