Nadine Girard

Stenting in Brain Hemodynamic Injury of Carotid Origin Caused by Type A Aortic Dissection: Local Experience and Systematic Literature Review

A. Jacquier, F. Collart, V. Gariboldi, 2022, Journal of personalized medicine.

Distal cerebral vasospasm treatment following aneurysmal subarachnoid hemorrhage using the Comaneci device: technical feasibility and single-center preliminary results

G. Boulouis, J. Stellmann, P. Dory-Lautrec, 2022, Journal of NeuroInterventional Surgery.

European recommendations on practices in pediatric neuroradiology: consensus document from the European Society of Neuroradiology (ESNR), European Society of Paediatric Radiology (ESPR) and European Union of Medical Specialists Division of Neuroradiology (UEMS)

J. Pruvo, P. Sundgren, C. Adamsbaum, 2022, Pediatric Radiology.

Automatic segmentation of deep grey nuclei using a high‐resolution 7T magnetic resonance imaging atlas—Quantification of T1 values in healthy volunteers

J. Ranjeva, M. Guye, L. de Rochefort, 2021, The European journal of neuroscience.

Computed tomography in the assessment of aneurysmal subarachnoid haemorrhage for clinical outcome: an observational cohort study

L. Velly, N. Bruder, H. Dufour, 2020 .

Clinicopathological and molecular characterization of three cases classified by DNA-methylation profiling as “Glioneuronal Tumors, NOS, Subtype A”

N. André, P. Varlet, N. Boddaert, 2022, Acta Neuropathologica.

A New Intra Arterial rt-PA Dosage Regimen in Peripheral Arterial Occlusion: Bolus Followed by Continuous Infusion

C. Juhan, S. Haupert, Nadine Girard, 1991, Thrombosis and Haemostasis.

Tumoral Hemorrhagic Stroke Revealing Carotid Angiosarcoma-Related Cerebral Metastases.

J. Stellmann, J. Hak, B. Testud, 2022, Neurology India.

Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome.

N. Philip, N. Girard, H. Sobol, 2015, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

David K. Wright, A. Sinclair, P. Kwan, 2023, Nature communications.