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Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

European journal of neurology, 2016-01, Vol.23 (1), p.45-52

2016

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Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study

American journal of neuroradiology : AJNR, 2012-06, Vol.33 (6), p.1102-1108

2012

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Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging

Journal of neurology, 2014, Vol.261 (1), p.27-36

2014

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Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Neurology, 2010-08, Vol.75 (7), p.619-625

2010

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Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

European journal of neurology, 2018-06, Vol.25 (6), p.861-868

2018

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Frontotemporal cortical thinning in amyotrophic lateral sclerosis

American journal of neuroradiology : AJNR, 2014-02, Vol.35 (2), p.304-310

2014

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TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2011-05, Vol.82 (5), p.587-588

2011

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The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features

European journal of neurology, 2010-05, Vol.17 (5), p.666-671

2010

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Subcortical motor plasticity in patients with sporadic ALS: An fMRI study

Brain research bulletin, 2006-05, Vol.69 (5), p.489-494

2006

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A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

Neuromuscular disorders : NMD, 2008-01, Vol.18 (1), p.68-70

2008

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Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen

Brain research, 1999-05, Vol.827 (1), p.205-209

1999

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Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders?

Journal of inherited metabolic disease, 2008-12, Vol.31 (Suppl 2), p.227-231

2008

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A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis

Journal of the American Academy of Dermatology, 1998-02, Vol.38 (2), p.344-348

1998

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Structure of Msj-1 Gene: A Comparative Analysis

Annals of the New York Academy of Sciences, 2005-04, Vol.1040 (1), p.406-409

2005

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Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals

Brain research, 1989-10, Vol.500 (1), p.90-98

1989

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Lan‐1: A Human Neuroblastoma Cell Line With M1 and M3 Muscarinic Receptor Subtypes Coupled to Intracellular Ca2+ Elevation and Lacking Ca2+ Channels Activated by Membrane Depolarization

Journal of neurochemistry, 1992-07, Vol.59 (1), p.1-9

1992

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Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy

American journal of medical genetics, 1987-04, Vol.26 (4), p.833-838

1987

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Accuracy of Death Certificates for Amyotrophic Lateral Sclerosis Varies Significantly from North to South of Italy: Implications for Mortality Studies

Neuroepidemiology, 2004-01, Vol.23 (1-2), p.73-77

2004

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High sensitivity method for fluorofore detection in gradient polyacrylamide slab gels through excitation by laser light: Application to glycoproteins stained with concanavalin A-fluorescein isothiocyanate

Analytical biochemistry, 1983-10, Vol.134 (2), p.313-319

1983

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Membrane depolarization in LA-N-1 cells: The effect of maitotoxin is Ca super(2+)- and Na super(+)-Dependent

Molecular and chemical neuropathology, 1997-04, Vol.30 (3), p.199-212

1997

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Lan-1: A human neuroblastoma cell line with M sub(1) and M sub(3) muscarinic receptor subtypes coupled to intracellular Ca super(2+) elevation and lacking Ca super(2+) channels activated by membrane depolarization

Journal of neurochemistry, 1992-01, Vol.59 (1), p.1-9

1992

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Membrane depolarization in LA-N-1 cells: The effect of maitotoxin is Ca2+- and Na+-dependent

Molecular and chemical neuropathology, 1997-04, Vol.30 (3), p.199-211

1997

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Determination of alimentary value of buffalo muscle proteins using enzymatic methods

Bollettino della Societa italiana di biologia sperimentale, 1976-07, Vol.52 (14), p.1082

1976

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Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent

Molecular and chemical neuropathology, 1997-04, Vol.30 (3), p.199

1997

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Lan‐1: A Human Neuroblastoma Cell Line With M 1 and M 3 Muscarinic Receptor Subtypes Coupled to Intracellular Ca 2+ Elevation and Lacking Ca 2+ Channels Activated by Membrane Depolarization

Journal of neurochemistry, 1992-07, Vol.59 (1), p.1-9

1992

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Tauroursodeoxycholic acid in the treatment of patients with amyotrophic lateral sclerosis

Widespread Microstructural White Matter Involvement in Amyotrophic Lateral Sclerosis: A Whole-Brain DTI Study

Distributed corpus callosum involvement in amyotrophic lateral sclerosis: a deterministic tractography study using q-ball imaging

Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis

Frontotemporal cortical thinning in amyotrophic lateral sclerosis

TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis

The GH-IGF system in amyotrophic lateral sclerosis: correlations between pituitary GH secretion capacity, insulin-like growth factors and clinical features

Subcortical motor plasticity in patients with sporadic ALS: An fMRI study

A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy

Establishment and characterization of a human neuroectodermal cell line (TB) from a cerebrospinal fluid specimen

Myasthenia gravis in a patient affected by glycogen storage disease type Ib: A further manifestation of an increased risk for autoimmune disorders?

A case of probable autosomal recessive ectodermal dysplasia with corkscrew hairs and mental retardation in a family with tuberous sclerosis

Structure of Msj-1 Gene: A Comparative Analysis

Direct inhibition of choline acetyltransferase activity by a monoclonal antibody raised against the plasma membrane of cholinergic nerve terminals

Lan‐1: A Human Neuroblastoma Cell Line With M1 and M3 Muscarinic Receptor Subtypes Coupled to Intracellular Ca2+ Elevation and Lacking Ca2+ Channels Activated by Membrane Depolarization

Phenotype heterogeneity among hemizygotes in a family biochemically screened for adrenoleukodystrophy

Accuracy of Death Certificates for Amyotrophic Lateral Sclerosis Varies Significantly from North to South of Italy: Implications for Mortality Studies

High sensitivity method for fluorofore detection in gradient polyacrylamide slab gels through excitation by laser light: Application to glycoproteins stained with concanavalin A-fluorescein isothiocyanate

Membrane depolarization in LA-N-1 cells: The effect of maitotoxin is Ca super(2+)- and Na super(+)-Dependent

Lan-1: A human neuroblastoma cell line with M sub(1) and M sub(3) muscarinic receptor subtypes coupled to intracellular Ca super(2+) elevation and lacking Ca super(2+) channels activated by membrane depolarization

Membrane depolarization in LA-N-1 cells: The effect of maitotoxin is Ca2+- and Na+-dependent

Determination of alimentary value of buffalo muscle proteins using enzymatic methods

Membrane depolarization in LA-N-1 cells. The effect of maitotoxin is Ca(2+)- and Na(+)-dependent

Lan‐1: A Human Neuroblastoma Cell Line With M 1 and M 3 Muscarinic Receptor Subtypes Coupled to Intracellular Ca 2+ Elevation and Lacking Ca 2+ Channels Activated by Membrane Depolarization

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