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Featured researches published by R. De Blasi.


Epilepsia | 1999

Metabolic Changes in Neuronal Migration Disorders: Evaluation by Combined MRI and Proton MR Spectroscopy

Isabella Laura Simone; F. Federico; Carla Tortorella; R. De Blasi; Rinaldo Bellomo; V. Lucivero; D. Carrara; A. Bellacosa; Paolo Livrea; A. Carella

Summary: Purpose: To assess the role of 1H‐magnetic resonance spectroscopy (MRS) in detecting biochemical abnormalities in neuronal migration disorders (NMDs).


Neurological Sciences | 2001

Paroxysmal dystonia with thalamic lesion in multiple sclerosis

A. Zenzola; M. De Mari; R. De Blasi; A. Carella; Paolo Lamberti

Abstract Paroxysmal dystonia (PD) is a usually painful, unilateral dystonic posture, precipitated by voluntary movement, tactile stimulation, startling noise or hyperventilation. We describe two cases of paroxysmal dystonia in multiple sclerosis, both with a critically localized lesion in the thalamus, contralateral to the paroxysmal symptoms. Only one other case of paroxysmal dystonia with a demyelinated lesion of the thalamus has been reported previously.


Neuroradiology | 2000

An unusual association of intracranial aneurysms and oesophageal duplication in a case of Klippel-Trenaunay syndrome.

R. De Blasi; A. Zenzola; C. M. Lanzilotti; Maurizio Resta; O. Caputi; Paolo Lamberti; F. Simone; M. T. Pangrazio; A. Carella

Abstract The Klippel-Trenaunay syndrome (KTS) is a congenital disorder resulting from a mesodermal abnormality, characterised by cutaneous capillary haemangiomas, hypertrophy of bone and soft tissues and varicose veins. The presence of intracranial aneurysms has rarely been described, while oesophageal duplication has not been reported previously. We describe a patient with the KTS with both there additional abnormalities, which could be explained by a postulated mosaic gene abnormality.


Interventional Neuroradiology | 1997

Endovascular treatment of a ruptured intracranial arterial aneurysm in a 12-year-old child with recessive polycystic kidney disease.

R. De Blasi; P. Lasjaunias; Georges Rodesch; H. Alvarez

A 12-year-old boy with recessive polycystic kidney disease and congenital hepatic failure, presented intracranial subarachnoid haemorrhage, due to the rupture of a laterobasilar tip aneurysm. In addition, he presented a left-sided middle cerebral unruptured aneurysm demonstrated during the screening procedure. Our patient is a boy, like most children with intracranial aneurysms, but differs from children with intracranial aneurysms in polycystic kidney disease. The age of bleeding was low (actually the second youngest case reported), with a good Hunt and Hess grade at admission. The localization of the aneurysm is exceptionally posterior (laterobasilar tip); in our case as intracranial aneurysms can be multifocal at that age. Renal function and blood pressure were normal. The endovascular GDC approach achieved a good result and excellent clinical outcome. Although most of what is known in this disease belongs to the autosomal dominant form, it is unclear whether the risk of a demonstrated unruptured intracranial aneurysm is the same as the risk of SAH from a non demonstrated one. It even seems that bleeding during follow-up in patients with polycystic kidney disease mostly occurs from non previously demonstrated intracranial aneurysms9.


Interventional Neuroradiology | 2009

A case of aneurysm on a persistent hypoglossal artery treated by endovascular coiling.

R. De Blasi; Nicola Medicamento; Luigi Chiumarulo; Andrea Salvati; Marilena Maghenzani; Franca Dicuonzo; A. Carella

We describe a 22-year-old woman admitted to hospital in emergency with nuchal headache and vomiting. CT scan disclosed subarachnoid hemorrhage. Digital subtraction angiography with three-dimensional rotational acquisitions showed a ruptured aneurysm of a right persistent primitive hypoglossal artery as the cause of symptoms and hemorrhage. The patient was successfully treated with endovascular coiling of the aneurysm. This is the second literature report describing endovascular treatment in this unusual condition.


Interventional Neuroradiology | 2010

Pseudoaneurysm Formation Following Intrasphenoid Rupture of an Idiopathic Intracavernous Carotid Artery Aneurysm: Coil Migration and Early Recurrence after Endovascular Treatment

R. De Blasi; E. Bracciolini; Luigi Chiumarulo; Andrea Salvati; C. Monetti; F. Federico; A. Carella

Intrasphenoid rupture of a non-traumatic aneurysm of the cavernous carotid artery is rare. We describe a patient in whom this condition manifested with epistaxis and led to the formation of a pseudoaneurysm occupying the right sphenoid sinus. The lesion recurred after repeated attempts at conservative endovascular therapy. Eventually the patient was treated with endovascular occlusion of the right internal carotid artery. Our report emphasizes the relapsing behaviour of a non-traumatic aneurysm of the cavernous portion of the internal carotid artery ruptured into the sphenoid sinus.


Rivista Di Neuroradiologia | 2009

Clinical Features and Classification of Brain AVMs and Cranial DAVFs.

R. De Blasi; Andrea Salvati; Nicola Medicamento; Luigi Chiumarulo

The clinical findings of intracranial vascular malformations are strictly related to their morphologic, angioarchitectural and hemodynamic characteristics. An overall study of these features is the first step to understand the different classifications for arteriovenous malformations, dural arteriovenous fistulas and carotid-cavernous fistulas. This evaluation will also suggest the correct timing of endovascular treatment and which part of the lesion should be the target of the therapy. Conventional cerebral angiography is mandatory when a correct classification of intracranial arteriovenous malformative shunts must be achieved. The angioarchitectural classification of brain arteriovenous malformations considers all angiographic features of each component of the malformation, both morphologically and hemodynamically, and relates them to the clinical course of the disease. The correlation between clinical findings, angiographic features and classifications is even stronger for cranial dural arteriovenous fistulas, in which cortical venous drainage is typical of “aggressive” fistulas and is usually absent in the “benign” type. Similarly, carotid-cavernous fistulas can be differentiated at angiography into high or low flow lesions according to the flow rate of the shunt, and into direct or indirect fistulas, according to the origin of arterial feeders. This paper focuses on the existing relation between the hemodynamics of brain arteriovenous malformations, cranial dural arteriovenous fistulas, carotid-cavernous fistulas, and their most frequent clinical findings, through an analysis of the most widely used different classification systems.


Rivista Di Neuroradiologia | 1994

An Approach with Neural Network to Detection of MRI Anatomy A Preliminary Report

R. De Blasi; A. Blonda; Guido Pasquariello; D. Milella; Franca Dicuonzo; A. Giancaspro; Giuseppe Satalino; A. Giannini; F. Ambrosi; A. Carella

In this paper an artificial modular system applied to object classification in brain MR images is presented. It consists of two modules based on neural architectures joined in sequence to perform first an image segmentation and then an object classification. For these two steps a Self Organizing Map and a Multilayer Perceptron trained with the Back-Propagation learning rule have been used. The objective of the system is the automatic recognition of the anatomic structures in MR images of the cerebral section passing through the orbits and the visual pathways. To reach this goal we have submitted the two networks to a training phase realized by an unsupervised process for the image segmentation and by a supervised process for regions labelling. This last step has been based on topographic relations supplied by a medical expert. The system has been useful to discriminate 20 different classes of anatomic objects over the considered section. Preliminary results are presented.


American Journal of Neuroradiology | 1991

CT AND MR STUDIES OF METHYLMALONIC ACIDEMIA

C.F. Andreula; R. De Blasi; A. Carella


Movement Disorders | 1996

Choreoathetosis in acquired immune deficiency syndrome patients with cerebral toxoplasmosis

P. Maggi; M. De Mari; R. De Blasi; S. Arminise; C. Romanelli; C.F. Andreula; G. Zimatore; G. Angarano

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