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Criteria for building types selection in preserved areas to pre-assess the Building Integrated Photovoltaics solar potential -The case study of Como land area

IOP conference series. Earth and environmental science, 2021-10, Vol.863 (1), p.12003

2021

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

Neurology, 1999-07, Vol.53 (1), p.38

1999

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The Influence of Technology Performance Durability in the Cost-Optimal Analysis of a ZEB

IOP conference series. Earth and environmental science, 2019-06, Vol.290 (1), p.12041

2019

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I-ZEB: Design and Development of a ZEB Test-Laboratory for an Integrated Evaluation of Building Technologies

IOP conference series. Earth and environmental science, 2019-06, Vol.290 (1), p.12092

2019

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Cost optimal analysis of energy refurbishment actions depending on the local climate and its variations

Mathematical Modelling of Engineering Problems, 2018-09, Vol.5 (3), p.268-274

2018

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

Gut, 1997-09, Vol.41 (3), p.411-412

1997

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Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

Acta neuropathologica, 1997-12, Vol.94 (6), p.567-571

1997

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

Neurology, 1997-05, Vol.48 (5), p.1200

1997

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Three-dimensional analysis of pulmonary nodules by MSCT with Advanced Lung Analysis (ALA1) software

Radiologia medica, 2006-04, Vol.111 (3), p.343-354

2006

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

American journal of neuroradiology : AJNR, 1994-10, Vol.15 (9), p.1721-1726

1994

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

Virchows Archiv : an international journal of pathology, 1995-12, Vol.427 (4), p.415-421

1995

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

Acta neurologica Scandinavica, 1995-11, Vol.92 (5), p.387-393

1995

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

Neuroradiology, 1994, Vol.36 (1), p.20-22

1994

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Neuronal intranuclear inclusion disease: neuropathologic study of a case

Brain & development (Tokyo. 1979), 1998-08, Vol.20 (5), p.290-294

1998

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

Biochemical and biophysical research communications, 1991-10, Vol.180 (2), p.887-893

1991

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Axonal motor and sensory neuropathy in myotonic dystrophy

Acta neurologica Scandinavica, 1993-08, Vol.88 (2), p.141-148

1993

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

Developmental medicine and child neurology, 1996-01, Vol.38 (1), p.65-73

1996

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1088Left-ventricular non-compaction: a multimodality imaging approach to trabeculation quantification allows refinement of diagnostic criteria

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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

Acta neurologica Scandinavica, 1996-07, Vol.94 (1), p.60-62

1996

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

Journal of the neurological sciences, 1995, Vol.128 (1), p.96-102

1995

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A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers

Brain & development (Tokyo. 1979), 1997-04, Vol.19 (3), p.209-211

1997

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Ultrastructural study of enteric ganglia in three patients with Rett syndrome

Brain & development (Tokyo. 1979), 1998-12, Vol.20 (8), p.586-588

1998

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Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

Journal of neurology, 1995-08, Vol.242 (8), p.490-496

1995

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

Brain & development (Tokyo. 1979), 1996, Vol.18 (1), p.59-63

1996

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

Child's nervous system, 1996-03, Vol.12 (3), p.155-160

1996

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Criteria for building types selection in preserved areas to pre-assess the Building Integrated Photovoltaics solar potential -The case study of Como land area

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

The Influence of Technology Performance Durability in the Cost-Optimal Analysis of a ZEB

I-ZEB: Design and Development of a ZEB Test-Laboratory for an Integrated Evaluation of Building Technologies

Cost optimal analysis of energy refurbishment actions depending on the local climate and its variations

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

Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

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

Three-dimensional analysis of pulmonary nodules by MSCT with Advanced Lung Analysis (ALA1) software

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

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

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

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

Neuronal intranuclear inclusion disease: neuropathologic study of a case

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

Axonal motor and sensory neuropathy in myotonic dystrophy

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

1088Left-ventricular non-compaction: a multimodality imaging approach to trabeculation quantification allows refinement of diagnostic criteria

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

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

A syndrome of autosomal recessive pontocerebellar hypoplasia with white matter abnormalities and protracted course in two brothers

Ultrastructural study of enteric ganglia in three patients with Rett syndrome

Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy

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

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

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