Publications by authors named "Maria C Bianchi"

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PRES-like leukoencephalopathy presenting with status epilepticus associated with Brentuximab Vedotin treatment.
Alessandro Orsini, Sayla Bernasconi, Maria Cristina Bianchi, Ilaria Trivelli, Maria Cristina Menconi

Acta Biomed· March 2022

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Multiple life-threatening relapses in a woman with primary angiitis of the central nervous system mimicking brain tumour: a case report.
Chiara Pizzanelli, Antonio Tavoni, Veronica Pelliccia, Eleonora Catarsi, Ilaria Pesaresi, Maria Cristina Bianchi

Clin Exp Rheumatol· July 2014

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A case of D-bifunctional protein deficiency: clinical, biochemical and molecular investigations.
Paolo Ghirri, Marco Vuerich, Sacha Ferdinandusse, Hans R Waterham, Andrea Guzzetta, Maria C Bianchi

Pediatr Int· August 2011

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Primary intra-diploic meningioma in a child.
Aldo Iannelli, Nicola Pieracci, Maria Cristina Bianchi, Francesca Becherini, Maura Castagna

Childs Nerv Syst· January 2008

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Influences of dopaminergic treatment on motor cortex in Parkinson disease: a MRI/MRS study.
Claudio Lucetti, Paulo Del Dotto, Gianna Gambaccini, Roberto Ceravolo, Chiara Logi, Maria Cristina Bianchi

Mov Disord· November 2007

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Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies.
Maria Cristina Bianchi, Giuseppina Sgandurra, Michela Tosetti, Roberta Battini, Giovanni Cioni

Biosci Rep· June 2007

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Age dependence of cerebral perfusion assessed by magnetic resonance continuous arterial spin labeling.
Laura Biagi, Arturo Abbruzzese, Maria Cristina Bianchi, David C Alsop, Alberto Del Guerra

J Magn Reson Imaging· April 2007

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Taylor-type focal cortical dysplasia: is the epilepsy always resistant to medical treatment?
Ennio Del Giudice, Maria Cristina Bianchi, Michela Tosetti, Andrea Varrone, Alfonso Romano

Epileptic Disord· December 2006

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Sensorineural deafness, hydrocephalus and structural brain abnormalities in two sisters: the Chudley-McCullough syndrome.
Fabio Matteucci, Enrico Tarantino, Maria Cristina Bianchi, Cristina Cingolani, Bruno Fattori

Am J Med Genet A· June 2006

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Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn: early treatment can prevent phenotypic expression of the disease.
Roberta Battini, M Grazia Alessandrì, Vincenzo Leuzzi, Francesca Moro, Michela Tosetti, Maria C Bianchi

J Pediatr· June 2006

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A mutation on exon 6 of guanidinoacetate methyltransferase (GAMT) gene supports a different function for isoform a and b of GAMT enzyme.
Vincenzo Leuzzi, Carla Carducci, Claudia Carducci, Maria Matricardi, Maria Cristina Bianchi

Mol Genet Metab· January 2006

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Creatine depletion in a new case with AGAT deficiency: clinical and genetic study in a large pedigree.
Roberta Battini, Vincenzo Leuzzi, Carla Carducci, Michela Tosetti, Maria C Bianchi

Mol Genet Metab· December 2002

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