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Hypoxic burden and sleep hypoventilation in obese patients

Sleep medicine, 2024-12, Vol.124, p.50-57

2024

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Migraine as possible red flag of PFO presence in suspected demyelinating disease

Journal of the neurological sciences, 2018-07, Vol.390, p.222-226

2018

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A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy

Journal of neurology, 2008-07, Vol.255 (7), p.1090-1092

2008

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Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entity

Neurology, 2003-10, Vol.61 (7), p.988-990

2003

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Adherence to anti-Parkinson drug therapy in the “REASON” sample of Italian patients with Parkinson’s disease: the linguistic validation of the Italian version of the “Morisky Medical Adherence scale-8 items”

Neurological sciences, 2013-11, Vol.34 (11), p.2015-2022

2013

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Modulation of cytokine production in activated human monocytes by somatostatin

Neuropeptides (Edinburgh), 1996-10, Vol.30 (5), p.443-451

1996

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Reasons driving treatment modification in Parkinson's disease: Results from the cross-sectional phase of the REASON study

Parkinsonism & related disorders, 2013-12, Vol.19 (12), p.1130-1135

2013

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pRb2/p130 Gene Overexpression Induces Astrocyte Differentiation

Molecular and cellular neuroscience, 2001-03, Vol.17 (3), p.415-425

2001

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Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

Neuropsychiatric disease and treatment, 2016-01, Vol.12, p.2497-2502

2016

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Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa-Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature

Neuropsychiatric disease and treatment, 2014-01, Vol.10, p.135-140

2014

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Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection

Neuropsychiatric disease and treatment, 2014-01, Vol.10 (default), p.2249-2252

2014

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Regenerated EDL muscle of rats requires innervation to maintain AChE molecular forms

Muscle & nerve, 1990-08, Vol.13 (8), p.713-721

1990

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Establishment of neuromuscular contacts in cultures of rat embryonic cells: effect of tetrodotoxin on maturation of muscle fibers and on formation and maintenance of acetylcholinesterase and acetylcholine receptor clusters

Developmental neuroscience, 1982-01, Vol.5 (4), p.314-325

1982

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The novel, catalytic mTORC1/2 inhibitor PQR620 and the PI3K/mTORC1/2 inhibitor PQR530 effectively cross the blood-brain barrier and increase seizure threshold in a mouse model of chronic epilepsy

Neuropharmacology, 2018-09, Vol.140, p.107-120

2018

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Light microscopic identification and immunocytochemical characterization of glutamatergic synapses in brain sections

Journal of comparative neurology (1911), 2005-11, Vol.492 (4), p.495-509

2005

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Non-canonical glutamate signaling in a genetic model of migraine with aura

Neuron (Cambridge, Mass.), 2021-02, Vol.109 (4), p.611-628.e8

2021

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Localization of neuroglobin in the brain of R6/2 mouse model of Huntington’s disease

Neurological sciences, 2018-02, Vol.39 (2), p.275-285

2018

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Increased expression of the astrocytic glutamate transporter GLT-1 in the prefrontal cortex of schizophrenics

Glia, 2005-02, Vol.49 (3), p.451-455

2005

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GABA transporters in the mammalian cerebral cortex: localization, development and pathological implications

Brain Research Reviews, 2004-07, Vol.45 (3), p.196-212

2004

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The glutamine commute: Lost in the tube?

Neurochemistry international, 2006-05, Vol.48 (6), p.459-464

2006

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Localization of the Glutamine Transporter SNAT1 in Rat Cerebral Cortex and Neighboring Structures, With a Note on its Localization in Human Cortex

Cerebral cortex (New York, N.Y. 1991), 2004-05, Vol.14 (5), p.562-574

2004

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Localization of the Na +-coupled neutral amino acid transporter 2 in the cerebral cortex

Neuroscience, 2006-01, Vol.140 (1), p.281-292

2006

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Unusual Stüve‐Wiedemann syndrome with complete maternal chromosome 5 isodisomy

Annals of clinical and translational neurology, 2014-11, Vol.1 (11), p.926-932

2014

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RB and RB2/P130 genes cooperate with extrinsic signals to promote differentiation of rat neural stem cells

Molecular and cellular neuroscience, 2007-03, Vol.34 (3), p.299-309

2007

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EAAC1 a high-affinity glutamate transporter, is localized to astrocytes and Gabaergic neurons besides pyramidal cells in the rat cerebral cortex

Cerebral cortex (New York, N.Y. 1991), 1998-03, Vol.8 (2), p.108-116

1998

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Hypoxic burden and sleep hypoventilation in obese patients

Migraine as possible red flag of PFO presence in suspected demyelinating disease

A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy

Charcot-Marie-Tooth disease with giant axons: a clinicopathological and genetic entity

Adherence to anti-Parkinson drug therapy in the “REASON” sample of Italian patients with Parkinson’s disease: the linguistic validation of the Italian version of the “Morisky Medical Adherence scale-8 items”

Modulation of cytokine production in activated human monocytes by somatostatin

Reasons driving treatment modification in Parkinson's disease: Results from the cross-sectional phase of the REASON study

pRb2/p130 Gene Overexpression Induces Astrocyte Differentiation

Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa-Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature

Foix-Chavany-Marie syndrome in a 17-year-old female with congenital cytomegalovirus infection

Regenerated EDL muscle of rats requires innervation to maintain AChE molecular forms

Establishment of neuromuscular contacts in cultures of rat embryonic cells: effect of tetrodotoxin on maturation of muscle fibers and on formation and maintenance of acetylcholinesterase and acetylcholine receptor clusters

The novel, catalytic mTORC1/2 inhibitor PQR620 and the PI3K/mTORC1/2 inhibitor PQR530 effectively cross the blood-brain barrier and increase seizure threshold in a mouse model of chronic epilepsy

Light microscopic identification and immunocytochemical characterization of glutamatergic synapses in brain sections

Non-canonical glutamate signaling in a genetic model of migraine with aura

Localization of neuroglobin in the brain of R6/2 mouse model of Huntington’s disease

Increased expression of the astrocytic glutamate transporter GLT-1 in the prefrontal cortex of schizophrenics

GABA transporters in the mammalian cerebral cortex: localization, development and pathological implications

The glutamine commute: Lost in the tube?

Localization of the Glutamine Transporter SNAT1 in Rat Cerebral Cortex and Neighboring Structures, With a Note on its Localization in Human Cortex

Localization of the Na +-coupled neutral amino acid transporter 2 in the cerebral cortex

Unusual Stüve‐Wiedemann syndrome with complete maternal chromosome 5 isodisomy

RB and RB2/P130 genes cooperate with extrinsic signals to promote differentiation of rat neural stem cells

EAAC1 a high-affinity glutamate transporter, is localized to astrocytes and Gabaergic neurons besides pyramidal cells in the rat cerebral cortex

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