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Differential Brain Network Activity Across Mood States in Bipolar Disorder

Journal of affective disorders, 2017-01, Vol.207, p.367-376

2017

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Intermittent theta burst stimulation of cerebellar vermis enhances fronto-cerebellar resting state functional connectivity in schizophrenia with predominant negative symptoms: A randomized controlled trial

Schizophrenia research, 2021-12, Vol.238, p.108-120

2021

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Bipolar Mood State Reflected in Cortico-Amygdala Resting State Connectivity: A Cohort and Longitudinal Study

Journal of affective disorders, 2017-08, Vol.217, p.205-209

2017

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State Dependent Cortico-Amygdala Circuit Dysfunction in Bipolar Disorder

Journal of affective disorders, 2016-09, Vol.201, p.79-87

2016

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Isolation of Distinct Networks Driving Action and Cognition in Psychomotor Processes

Biological psychiatry (1969), 2024-03

2024

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Screening for pharmacological chaperones in Fabry disease

Biochemical and biophysical research communications, 2007-07, Vol.359 (1), p.168-173

2007

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Lysosomal α-Galactosidase Controls the Generation of Self Lipid Antigens for Natural Killer T Cells

Immunity (Cambridge, Mass.), 2010-08, Vol.33 (2), p.216-228

2010

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Development of a model system for neuronal dysfunction in Fabry disease

Molecular genetics and metabolism, 2016-09, Vol.119 (1-2), p.144-150

2016

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Fabry disease in childhood

The Journal of pediatrics, 2004-05, Vol.144 (5), p.S20-S26

2004

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A validated disease severity scoring system for Fabry disease

Molecular genetics and metabolism, 2010-03, Vol.99 (3), p.283-290

2010

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The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease

The Journal of pediatrics, 2001-04, Vol.138 (4), p.539-547

2001

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Establishment and characterization of Fabry disease endothelial cells with an extended lifespan

Molecular genetics and metabolism, 2007-09, Vol.92 (1), p.137-144

2007

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Normal hearing in α-galactosidase A-deficient mice, the mouse model for Fabry disease

Hearing research, 2007-12, Vol.234 (1), p.10-14

2007

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Improved intracellular delivery of glucocerebrosidase mediated by the HIV-1 TAT protein transduction domain

Biochemical and biophysical research communications, 2005-11, Vol.337 (2), p.701-707

2005

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Expression and secretion of human glucocerebrosidase mediated by recombinant lentivirus vectors in vitro and in vivo: implications for gene therapy of Gaucher disease

Biochemical and biophysical research communications, 2004-05, Vol.318 (2), p.381-390

2004

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Medical bioremediation: prospects for the application of microbial catabolic diversity to aging and several major age-related diseases

Ageing research reviews, 2005-08, Vol.4 (3), p.315-338

2005

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Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase

Mutation research, 2001-11, Vol.483 (1-2), p.89

2001

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Cocaine Detoxification by Human Plasma Butyrylcholinesterase

Toxicology and applied pharmacology, 1997-08, Vol.145 (2), p.363-371

1997

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Enzymatic and functional correction along with long-term enzyme secretion from transduced bone marrow hematopoietic stem/progenitor and stromal cells derived from patients with Fabry disease

Experimental hematology, 1999-07, Vol.27 (7), p.1149-1159

1999

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A prospective 10 year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S103-S103

2015

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A prospective 10year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S103

2015

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Molecular Cloning and Chromosomal Mapping of the Mouse Gene Encoding Cyclin-Dependent Kinase 5 Regulatory Subunit p35

Genomics (San Diego, Calif.), 1996-07, Vol.35 (2), p.372-375

1996

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Lysosomal [alpha]-Galactosidase Controls the Generation of Self Lipid Antigens for Natural Killer T Cells

Immunity (Cambridge, Mass.), 2010-08, Vol.33 (2), p.216

2010

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Type C Niemann-Pick disease: A murine model of the lysosomal cholesterol lipidosis accumulates sphingosine and sphinganine in liver

Biochimica et biophysica acta, 1992-08, Vol.1127 (3), p.303-311

1992

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The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterol

BBA - Molecular Basis of Disease, 1994-02, Vol.1225 (3), p.235-243

1994

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Differential Brain Network Activity Across Mood States in Bipolar Disorder

Intermittent theta burst stimulation of cerebellar vermis enhances fronto-cerebellar resting state functional connectivity in schizophrenia with predominant negative symptoms: A randomized controlled trial

Bipolar Mood State Reflected in Cortico-Amygdala Resting State Connectivity: A Cohort and Longitudinal Study

State Dependent Cortico-Amygdala Circuit Dysfunction in Bipolar Disorder

Isolation of Distinct Networks Driving Action and Cognition in Psychomotor Processes

Screening for pharmacological chaperones in Fabry disease

Lysosomal α-Galactosidase Controls the Generation of Self Lipid Antigens for Natural Killer T Cells

Development of a model system for neuronal dysfunction in Fabry disease

Fabry disease in childhood

A validated disease severity scoring system for Fabry disease

The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher’s disease

Establishment and characterization of Fabry disease endothelial cells with an extended lifespan

Normal hearing in α-galactosidase A-deficient mice, the mouse model for Fabry disease

Improved intracellular delivery of glucocerebrosidase mediated by the HIV-1 TAT protein transduction domain

Expression and secretion of human glucocerebrosidase mediated by recombinant lentivirus vectors in vitro and in vivo: implications for gene therapy of Gaucher disease

Medical bioremediation: prospects for the application of microbial catabolic diversity to aging and several major age-related diseases

Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase

Cocaine Detoxification by Human Plasma Butyrylcholinesterase

Enzymatic and functional correction along with long-term enzyme secretion from transduced bone marrow hematopoietic stem/progenitor and stromal cells derived from patients with Fabry disease

A prospective 10 year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease

A prospective 10year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease

Molecular Cloning and Chromosomal Mapping of the Mouse Gene Encoding Cyclin-Dependent Kinase 5 Regulatory Subunit p35

Lysosomal [alpha]-Galactosidase Controls the Generation of Self Lipid Antigens for Natural Killer T Cells

Type C Niemann-Pick disease: A murine model of the lysosomal cholesterol lipidosis accumulates sphingosine and sphinganine in liver

The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterol

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