A. M. Paula

发表

Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosis

O. Chinot, D. Figarella-Branger, A. Barlier, 2010, Acta Neuropathologica.

IDH mutation status impact on in vivo hypoxia biomarkers expression: new insights from a clinical, nuclear imaging and immunohistochemical study in 33 glioma patients

O. Chinot, D. Figarella-Branger, E. Guedj, 2011, Journal of Neuro-Oncology.

Acute motor and sensory axonal neuropathy and concomitant encephalopathy during tumor necrosis factor-alpha antagonist therapy

J. Pouget, J. Franques, A. M. Paula, 2010, Journal of the Neurological Sciences.

A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibers

A. Chaussenot, S. Bannwarth, A. M. Paula, 2016, Neuromuscular Disorders.

A TPM3 mutation causing cap myopathy

D. Figarella-Branger, J. Pouget, N. Monnier, 2009, Neuromuscular Disorders.

Molecular genetics of adult grade II gliomas: towards a comprehensive tumor classification system

O. Chinot, D. Figarella-Branger, C. Colin, 2012, Journal of Neuro-Oncology.

Primary neurolymphomatosis diagnosis and treatment: A retrospective study

O. Chinot, J. Pouget, E. Tabouret, 2014, Journal of the Neurological Sciences.

Meningeal Rosai–Dorfman disease mimicking meningioma

D. Figarella-Branger, P. Metellus, A. M. Paula, 2013, Annals of Hematology.

Interpretation of epileptogenic lesions: Its limitations in medico-legal experts’ reports

A. M. Paula, C. Boval, G. Léonetti, 2021 .

Sporadic diffuse leucoencephalopathy with axonal spheroids: report of a profuse and rapid cortical–spinal degeneration

D. Dickson, Z. Wszolek, A. M. Paula, 2012, Neurological Sciences.

Myofibrillar myopathies: State of the art, present and future challenges.

I. Nelson, D. Figarella-Branger, N. Romero, 2015, Revue neurologique (Paris).

Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia

D. Figarella-Branger, J. Pouget, M. Krahn, 2006, Neurology.

Camptocormia as presenting sign in myofibrillar myopathy

B. Udd, A. M. Paula, G. Castelnovo, 2012, Neuromuscular Disorders.

[Pituitary melanocytoma mimicking an adenoma].

D. Figarella-Branger, H. Dufour, B. Coulibaly, 2011, Annales de pathologie.

Myofibrillar myopathies: State of the art, present and future challenges.

I. Nelson, D. Figarella-Branger, N. Romero, 2015, Revue neurologique.

Myofibrillar myopathies: State of the art, present and future challenges.

I. Nelson, D. Figarella-Branger, N. Romero, 2015, Revue neurologique.

Atypical teratoid/rhabdoid tumour: 7-year event-free survival with gross total resection and radiotherapy in a 7-year-old boy

D. Figarella-Branger, A. M. Paula, C. Bouvier, 2007, Child's Nervous System.

A TPM3 mutation causing cap myopathy

D. Figarella-Branger, J. Pouget, N. Monnier, 2009, Neuromuscular Disorders.