G. Guazzi

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Thalamo‐cortical connections of the first and second somatic sensory areas in the cat

G. Macchi, F. Angeleri, G. Guazzi, 1959, The Journal of comparative neurology.

The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.

G. Guazzi, A. Federico, G. Grieco, 1996, Journal of neurology, neurosurgery, and psychiatry.

Axonal motor and sensory neuropathy in myotonic dystrophy

G. Guazzi, A. Malandrini, M. Mondelli, 1993, Acta neurologica Scandinavica.

Involvement of peripheral sensory fibers in amyotrophic lateral sclerosis: Electro‐physiological study of 64 cases

A. Rossi, G. Guazzi, S. Passero, 1993, Muscle & nerve.

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.

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

N. Battistini, G. Guazzi, P. Righetti, 1999, Neurology.

CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study

G. Guazzi, A. Malandrini, M. Villanova, 1998, European Neurology.

Cherry-red spot myoclonus syndrome (type I sialidosis).

G. Guazzi, A. Federico, N. Stefano, 1991, Developmental neuroscience.

Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.

A. Rossi, C. Scarpini, G. Guazzi, 1995, Electromyography and clinical neurophysiology.

Sensory-motor chronic neuropathy in two siblings: atypical presentation of tomaculous neuropathy.

G. Guazzi, A. Federico, A. Malandrini, 1992, Clinical neuropathology.

Type I Sialidosis: A Clinical, Biochemical and Neuroradiological Study

G. Guazzi, A. Malandrini, M. Villanova, 2000, European Neurology.

IL-6 detection in multiple sclerosis brain

G. Guazzi, D. Maimone, P. Annunziata, 1997, Journal of the Neurological Sciences.

Adrenomyeloneurodystrophy with late cerebral involvement and evidence of a multiple autoimmune disorder

U. Bonuccelli, G. Guazzi, A. Malandrini, 1988, Journal of Inherited Metabolic Disease.

Association of polyclonal anti‐GM1 IgM and anti‐neurofilament antibodies with CSF oligoclonal bands in a young with amyotrophic lateral sclerosis

G. Guazzi, D. Maimone, P. Annunziata, 1995, Acta neurologica Scandinavica.

MERRF syndrome . mitochondrial tRNALeu ( UUR ) may cause an The A to G transition at nt 3243 of the

G. Guazzi, A. Federico, G. Grieco, 2003 .

Charcot-Marie-Tooth disease: an intermediate form

C. Broeckhoven, G. Guazzi, A. Malandrini, 1998, Neuromuscular Disorders.

Autosomal recessive paraparesis with amyotrophy of hands and feet and white matter lesions

C. Scarpini, G. Guazzi, A. Malandrini, 1996, Acta neurologica Scandinavica.

Inheritance of a 38‐kb fragment in apparently sporadic facioscapulohumeral muscular dystrophy

F. Vitelli, G. Guazzi, A. Malandrini, 1999, Muscle & nerve.

Type 3 (chronic) GM1 gangliosidosis presenting as infanto‐choreo‐athetotic dementia, without epilepsy, in three sisters

G. Guazzi, A. Federico, F. Van hoof, 1988, Neurology.

Frequency of blood-retina and blood-brain barrier changes in multiple sclerosis

G. Guazzi, U. Menchini, P. Annunziata, 1988, The Italian Journal of Neurological Sciences.

Interleukin-6 levels in the cerebrospinal fluid and serum of patients with Guillain-Barré syndrome and chronic inflammatory demyelinating polyradiculoneuropathy

G. Guazzi, P. Livrea, I. Simone, 1993, Journal of Neuroimmunology.

Detection of Borrelia burgdorferi DNA and complement membrane attack complex deposits in the sural nerve of a patient with chronic polyneuropathy and tertiary lyme disease

S. Bonin, G. Guazzi, A. Malandrini, 1997, Muscle & nerve.

Pseudo-tumoural presentation of certain cases of subacute sclerosing leucoencephalitis.

G. Guazzi, J. Głowacki, L. V. van Bogaert, 1967, Journal of the neurological sciences.

Eosinophilia myalgia syndrome: absence of immunoglobulin reactivity suggests a cellular rather than humoral mechanism.

J. Martín, P. Cras, G. Guazzi, 1994, Acta neurologica Belgica.

GM2 gangliosidosis with hexosaminidase A and B defect: Report of a family with motor neuron disease-like phenotype

A. Rossi, G. Guazzi, A. Federico, 1986, Journal of Inherited Metabolic Disease.

Serum anti-brain endothelium antibodies and cognitive assessment in patients with Binswanger's encephalopathy

G. Guazzi, F. Moschini, P. Annunziata, 1995, Journal of the Neurological Sciences.

Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defect

P. Zaniol, B. Barbiroli, R. Lodi, 1996, Journal of the Neurological Sciences.

Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter

C. Scarpini, G. Guazzi, A. Malandrini, 1995, Journal of the Neurological Sciences.

Juvenile dystonia without vertical gaze paralysis: Niemann-Pick type C disease

G. Guazzi, A. Federico, S. Palmeri, 1986, Journal of Inherited Metabolic Disease.

Early synthesis and correlation of serum anti-thyroid antibodies with clinical parameters in multiple sclerosis

G. Guazzi, E. Guarino, S. Borghi, 1999, Journal of the Neurological Sciences.

Urinary oligosaccharides in lysosomal and other metabolic disorders

G. Guazzi, A. Federico, Giancarlo Guazzi, 1982, The Italian Journal of Neurological Sciences.

Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren)

J. Martín, G. Guazzi, A. Malandrini, 1999, Acta Neuropathologica.

The clinical aspects of adult hexosaminidase deficiencies.

G. Guazzi, A. Malandrini, A. Federico, 1991, Developmental neuroscience.

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.

Wolman's disease.

J. Martín, G. Guazzi, H. Roels, 1968, European neurology.

Acanthocytosis, retinitis pigmentosa, pallidal degeneration. Report of two cases without serum lipid abnormalities

G. Guazzi, A. Malandrini, M. Villanova, 1996, Journal of the Neurological Sciences.

Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia

G. Guazzi, A. Federico, F. Cornelio, 1988, The Italian Journal of Neurological Sciences.

Myopathic involvement in two cases of Hallervorden-Spatz disease

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

Lymphocyte activating factor activity in the serum and cerebrospinal fluid of patients with multiple sclerosis

G. Guazzi, D. Boraschi, A. Tagliabue, 1990, The Italian Journal of Neurological Sciences.

Cerebro-ocular dysplasia and muscular dystrophy: report of two cases.

G. Guazzi, A. Malandrini, A. Federico, 1988, Neuropediatrics.

Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.

B. Ghetti, G. Guazzi, A. Amati, 1971, Acta geneticae medicae et gemellologiae.

Neuronal intranuclear inclusion disease: neuropathologic study of a case

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

Wolman's disease. Distribution and significance of the central nervous system lesions.

J. Martín, G. Guazzi, H. Roels, 1968, Pathologia Europaea.

HTLV-I-ASSOCIATED SPASTIC PARAPARESIS IN AN ITALIAN WOMAN

G. Guazzi, G. Fanetti, P. Annunziata, 1987, The Lancet.

[On the significance of aspects of recurring and granulomatous phlebitis in the cerebral manifestations of Behcet's disease].

G. Guazzi, J. Floquet, P. Tridon, 1966, Revue neurologique.

Sanfilippo A syndrome (Mucopolysaccharidosis III A): a neurochemical study

G. Guazzi, A. Federico, J. Robert, 1981, The Italian Journal of Neurological Sciences.

Palatal myoclonus and unusual MRI findings in a patient with membranous lipodystrophy

C. Scarpini, G. Guazzi, A. Malandrini, 1996, Brain and Development.

Normal rhodanese activity in leukocytes from Leber patients

G. Guazzi, A. Federico, P. Martelli, 1987, Neurology.

Changes of brain glyco-conjugates in Unverricht-Lundborg's disease.

G. Guazzi, A. Federico, R. Corona, 1978, Acta neurologica.

Glycosaminoglycans and glycoproteins in metachromatic leucodystrophy.

G. Guazzi, A. Federico, C. Di Benedetta, 1977, European neurology.

Mycolonus epilepsy with cherry-red spot in adult: a peculiar form of mucopolysaccharidosis. (A clinical genetic, chemical and ultrastructural study).

B. Ghetti, G. Guazzi, F. Barbieri, 1973, Acta neurologica.

[Natural history of the spongy state. Its significance in optic cytopathology].

G. Guazzi, L. V. van Bogaert, H. Ishino, 1968, Archiv fur Psychiatrie und Nervenkrankheiten.

Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency

C. Broeckhoven, J. Six, G. Guazzi, 1996, Neuromuscular Disorders.

Optic atrophy in Marinesco-Sjögren syndrome: an additional ocular feature. Report of three cases in two families.

G. Guazzi, A. Malandrini, A. Federico, 1993, Ophthalmic paediatrics and genetics.

Neurologie et neuropathologie du syndrome de lowe

G. Guazzi, C. Hooft, J. Herpol, 1966 .

[Particles of viral aspect seen in electron microscopy in a cerebral biopsy of Schilder's diffuse peri-axile encephalitis].

G. Guazzi, R. Houdart, M. Bouteille, 1966, La Presse medicale.

Increase of predominantly k-type light chains in the CSF of a case of subacute sclerosing panencephalitis treated with interferon

G. Guazzi, P. Annunziata, A. Battista, 1985, The Italian Journal of Neurological Sciences.

Charcot-Marie-Tooth disease: study of a large kinship with an intermediate form

A. Rossi, G. Guazzi, C. Paradiso, 2004, Journal of Neurology.

Hypoplasia of the corpus callosum in Niemann-Pick type C disease

G. Guazzi, A. Federico, C. Battisti, 2004, Neuroradiology.

Cloning and sequence analysis of the human liver rhodanese: comparison with the bovine and chicken enzymes.

G. Guazzi, M. Cacace, C. Cannella, 1991, Biochemical and biophysical research communications.

Electrocardiographic abnormalities in Leber's hereditary optic atrophy

G. Guazzi, A. Federico, M. Dotti, 1987, Journal of Inherited Metabolic Disease.

[Congenital familial spongy idiocy (van Bogaert-Bertrand syndrome) in a non-Jewish family (study of a 2d Italian family)].

G. Guazzi, G. Giordano, G. Salvati, 1969, Acta geneticae medicae et gemellologiae.

Cerebrotendinous xanthomatosis (van Bogaert-Scherer-Epstein disease): CT and MR findings.

G. Guazzi, A. Federico, M. Dotti, 1994, AJNR. American journal of neuroradiology.

Sudanophilic leucodystrophy with meningeal angiomatosis in two brothers: infantile form of diffuse sclerosis with meningeal angiomatosis.

G. Guazzi, L. V. van Bogaert, C. Hooft, 1965, Journal of Neurological Sciences.

Infantile form of meningeal angiomatosis with sudanophilic leucodystrophy associated with complex abiotrophies. Study of a second family.

J. Martín, G. Guazzi, J. Bruens, 1968, Journal of the neurological sciences.

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.

Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families.

G. Guazzi, A. Federico, M. Dotti, 1989, Acta neurologica.

Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study.

F. Muntoni, J. Six, G. Guazzi, 1997, Acta neuropathologica.

Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency.

J. Six, J. Martín, G. Guazzi, 1996, Journal of submicroscopic cytology and pathology.

Localization of the laminin α2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

J. Six, G. Guazzi, A. Malandrini, 1997, Acta Neuropathologica.

Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects.

G. Guazzi, A. Malandrini, N. Maraldi, 1997, Neuromuscular Disorders.

Intracellular detection of laminin α 2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α 2 chain deficient subjects

G. Guazzi, A. Malandrini, A. Pini, 1997, Neuromuscular Disorders.

[Histochemical and ultrastructural findings in a case of multiple sclerosis associated with a spongioblastoma].

G. Guazzi, L. Martin, M. Bouteille, 1967, Rivista di patologia nervosa e mentale.

The potential role of hepatitis C virus in the pathogenesis of the neurological syndrome in chronic hepatitis C

G. Guazzi, D. Maimone, P. E. Valensin, 1997, Gut.

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy

M. Zeviani, G. Guazzi, A. Malandrini, 1996, Acta Neuropathologica.

An unusual type of primary cerebral hemihypotrophy with signs of dysfunctional neuronal migration

G. Guazzi, A. Malandrini, M. Villanova, 1996, Acta Neuropathologica.

Congenital lactic acidosis due to a defect of pyruvate dehydrogenase complex (E1). Clinical, biochemical, nerve biopsy study and effect of therapy.

G. Guazzi, A. Malandrini, A. Federico, 1990, European neurology.

TheA toG transition atnt3243ofthe mitochondrial tRNALeu(uuR) maycauseanMERRF syndrome

G. Guazzi, A. Federico, G. Grieco, 1996 .

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.

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy

G. Guazzi, A. Malandrini, M. Villanova, 1997, Neurology.

Anti-HTLV-I antibodies in the serum and CSF from amyotrophic lateral sclerosis patients: negative findings

G. Guazzi, G. Fanetti, A. D’Andrea, 1989, Journal of Neurology.

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.

Intrathecal synthesis of anti‐myelin basic protein IgG in HIV‐1+ patients

G. Guazzi, D. Maimone, P. Annunziata, 1994, Acta neurologica Scandinavica.

Giant axonal neuropathy in 2 siblings: a generalized disorder of intermediate filaments.

G. Guazzi, A. Malandrini, A. Federico, 1991, European neurology.

ATAXIA‐TELANGIECTASIA: SOMATOSENSORY,‘BRAINSTEM AUDITORY. AND MOTOR EVOKED POTENTIALS IN SIX PATIENTS

C. Scarpini, G. Guazzi, A. Federico, 1996, Developmental medicine and child neurology.

Macular cherry-red spot and myoclonus syndrome Juvenile form of sialidosis

G. Guazzi, A. Federico, G. Strecker, 1980, Journal of the Neurological Sciences.

Glycopeptidosis: A new inherited disorder of glycoconjugate metabolism affecting the central nervous system

G. Guazzi, A. Federico, G. Strecker, 1981, Journal of Inherited Metabolic Disease.

Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome?

G. Guazzi, A. Malandrini, R. Di Perri, 1994, American journal of medical genetics.

Schilder's diffuse sclerosis.

J. Martín, G. Guazzi, J. Martin, 1991, Developmental neuroscience.

Ultrastructural microscopy of different types of nuclear and cytoplasmic inclusions in subacute sclerosing leucoencephalitis

G. Guazzi, L. Martin, M. Bouteille, 1968 .

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.

Cytogenetic studies of three families with ataxia-telangiectasia (Louis-Bar syndrome)

G. Guazzi, A. Federico, L. Chessa, 1986, Journal of Inherited Metabolic Disease.

Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

V. Tiranti, M. Zeviani, G. Guazzi, 1995, Journal of Neurology.

Ultrastructural study of enteric ganglia in three patients with Rett syndrome

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

Clinical and Neurophysiological Changes in Carriers from a Family with Type O Chronic GM2-Gangliosidosis with Als Phenotype

A. Rossi, G. Guazzi, A. Federico, 1988 .