G. Berti

发表

Mitochondrial Abnormalities in Genetically Assessed Oculopharyngeal Muscular Dystrophy

F. Ginanneschi, A. Malandrini, A. Federico, 2004, European Neurology.

Ultrastructure and immunoreactivity of dystrophic axons indicate a different pathogenesis of Hallervorden-Spatz disease and infantile neuroaxonal dystrophy

G. Guazzi, A. Malandrini, G. Fabrizi, 2004, Virchows Archiv.

Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy

C. Reggiani, G. Siciliano, A. Malandrini, 2017, Human mutation.

Electron‐dense lamellated inclusions in 2 siblings with Kufor–Rakeb syndrome

A. Federico, A. Malandrini, C. Battisti, 2013, Movement disorders : official journal of the Movement Disorder Society.

Typical pathological changes of CADASIL in the optic nerve

A. Federico, A. Malandrini, M. Dotti, 2005, Neurological Sciences.

PAX6 mutation in a family with aniridia, congenital ptosis, and mental retardation

A. Malandrini, A. Renieri, F. Mari, 2001, Clinical genetics.

Is myopathy with rimmed vacuoles a hallmark of juvenile neuronal ceroid lipofuscinosis (CLN3)?

M. Lo Giudice, A. Malandrini, S. Musumeci, 2016, Neurological Sciences.

DIAGNOSTIC VALUE OF ULTRASTRUCTURAL SKIN BIOPSY STUDIES IN CADASIL

A. Federico, A. Malandrini, A. Federico, 2007, Neurology.

Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL

A. Malandrini, M. Villanova, F. Albani, 2002, Neurology.

Muscle Biopsy and In Vitro Contracture Test in Subjects with Idiopathic HyperCKemia

A. Federico, A. Malandrini, M. Dotti, 2008, Anesthesiology.

Dissolution of calcium pyrophosphate crystals by polyphosphates: an in vitro and ex vivo study

R. Cini, E. Selvi, S. Lorenzini, 2001, Annals of the rheumatic diseases.

Neuropathological findings associated with retained lead shot pellets in a man surviving two months after a suicide attempt.

M. Di Paolo, A. Malandrini, M. Villanova, 2001, Journal of forensic sciences.

Atypical McLeod syndrome manifested as X-linked chorea-acanthocytosis, neuromyopathy and dilated cardiomyopathy: report of a family

G. Guazzi, A. Malandrini, G. D. Pietro, 1994, Journal of the Neurological Sciences.

Choreo-acanthocytosis like phenotype without acanthocytes: clinicopathological case report

A. Federico, A. Malandrini, G. Fabrizi, 1993, Acta Neuropathologica.

Myopathic involvement in two cases of Hallervorden-Spatz disease

U. Bonuccelli, G. Guazzi, A. Malandrini, 1995, Brain and Development.

Neuronal intranuclear inclusion disease: neuropathologic study of a case

G. Guazzi, A. Malandrini, M. Villanova, 1998, Brain and Development.

Inclusion Body Myopathy-Like Changes in a Family with Cerebellar Atrophy, Mental Retardation and Abnormal Pupils

A. Malandrini, A. Federico, M. Dotti, 2006, European Neurology.

A syndrome of bilateral hemorrhage of the thalamus and myocarditis with fatal course.

M. Di Paolo, A. Malandrini, A. Federico, 2004, Journal of clinical forensic medicine.

Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNALeu(CUN) mutation of mitochondrial DNA

E. Malfatti, A. Malandrini, A. Federico, 2008, Journal of the Neurological Sciences.

A case of spastic paraplegia type 11 mimicking a GM2-gangliosidosis

E. Bertini, A. Federico, A. Malandrini, 2022, Neurological Sciences.

A novel heteroplasmic tRNASer(UCN) mtDNA point mutation associated with progressive external ophthalmoplegia and hearing loss

E. Malfatti, A. Federico, A. Malandrini, 2007, Neuromuscular Disorders.

Neuronal intranuclear inclusion disease: Polymerase chain reaction and ultrastructural study of rectal biopsy specimen in a new case

G. Guazzi, M. Zazzi, A. Malandrini, 2009, Acta Neuropathologica.

Amyloid Arthropathy: When the Rheumatologist Meets the Hematologist.

E. Selvi, G. Guidelli, M. Bardelli, 2016, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

M. Zeviani, E. Malfatti, A. Federico, 2009, European Journal of Human Genetics.

Clinicopathological study of familial late infantile Hallervorden-Spatz disease: a particular form of neuroacanthocytosis

G. Guazzi, A. Malandrini, G. Fabrizi, 1996, Child's Nervous System.

Autonomic nervous system and smooth muscle cell involvement in systemic sclerosis: ultrastructural study of 3 cases.

G. Guazzi, A. Malandrini, M. Villanova, 2000, The Journal of rheumatology.

Peripheral neuropathy in late-onset Krabbe disease: report of three cases

A. Federico, A. Malandrini, M. Dotti, 2012, Neurological Sciences.

Ultrastructural findings in the peripheral nerve in a family with the intermediate form of Charcot-Marie-Tooth disease.

G. Guazzi, A. Malandrini, M. Villanova, 2001, Journal of submicroscopic cytology and pathology.

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis

A. Federico, A. Quattrone, A. Malandrini, 2008, Brain and Development.

Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype

A. Malandrini, A. Federico, M. Muglia, 2005, Neurology.

Ultrastructural study of enteric ganglia in three patients with Rett syndrome

G. Guazzi, A. Malandrini, M. Villanova, 1998, Brain & development (Tokyo. 1979).

CCDC78: unveiling the function of a novel gene associated to hereditary myopathy

D. Lopergolo, G. Gallus, F. Boscaro, 2023, medRxiv.