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Telomere length and mitochondrial DNA copy number in bipolar disorder: identification of a subgroup of young individuals with accelerated cellular aging

Translational psychiatry, 2022-04, Vol.12 (1), p.135-135, Article 135

2022

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Signal Transduction through Prion Protein

Science (American Association for the Advancement of Science), 2000-09, Vol.289 (5486), p.1925-1928

2000

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Acute pain Factors predictive of post-operative pain and opioid requirement in multimodal analgesia following knee replacement

European journal of pain, 2016-05, Vol.20 (5), p.822-832

2016

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Amplification techniques and diagnosis of prion diseases

Revue neurologique, 2019-09, Vol.175 (7-8), p.458-463

2019

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Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov

Archives of virology, 1999-01, Vol.144 (3), p.431-445

1999

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Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

Neurology, 2000-09, Vol.55 (6), p.811

2000

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Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

Neurology, 2010-06, Vol.74 (24), p.1995

2010

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A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion

Neuropathology and applied neurobiology, 2011-08, Vol.37 (5), p.554-559

2011

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Long-standing Prion Dementia Manifesting as Posterior Cortical Atrophy

Alzheimer disease and associated disorders, 2012-07, Vol.26 (3), p.289-292

2012

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Functional expression of p-glycoprotein and multidrug resistance-associated protein (mrp1) in primary cultures of rat astrocytes

Journal of neuroscience research, 2000-06, Vol.60 (5), p.594-601

2000

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Telomere length and mitochondrial DNA copy number in bipolar disorder: A sibling study

The world journal of biological psychiatry, 2023-06, Vol.24 (5), p.449-456

2023

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Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects

Neurology, 2004-12, Vol.63 (12), p.2413

2004

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Variant or sporadic Creutzfeldt-Jakob disease?

The Lancet (British edition), 2010-03, Vol.375 (9718), p.889-889

2010

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A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

Neurology, 2005-04, Vol.64 (8), p.1455

2005

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Alzheimer's disease cerebro-spinal fluid biomarkers: A clinical research tool sometimes useful in daily clinical practice of memory clinics for the diagnosis of complex cases

La revue de medecine interne, 2017-04, Vol.38 (4), p.250-255

2017

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Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

Molecular psychiatry, 2002, Vol.7 (1), p.67-71

2002

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Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes

Neuropathology and applied neurobiology, 2011-08, Vol.37 (5), p.500-512

2011

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Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates

Neurology, 2000-03, Vol.54 (5), p.1095

2000

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Antidepressant-induced mania, rapid cycling and the serotonin transporter gene polymorphism

The pharmacogenomics journal, 2003-01, Vol.3 (2), p.101-104

2003

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Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice

Clinica chimica acta, 2019-08, Vol.495, p.451-456

2019

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Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders

Biological psychiatry (1969), 2000-08, Vol.48 (4), p.319-322

2000

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Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression

Neuroscience letters, 1998-10, Vol.255 (3), p.143-146

1998

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Fatal familial insomnia presenting as psychosis in an 18-year-old man

Neurology, 2006-07, Vol.67 (2), p.363

2006

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14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

Dementia and geriatric cognitive disorders, 1999-01, Vol.10 (1), p.40

1999

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Diagnostic value of CSF 14-3-3 detection in sporadic CJD diagnosis according to the age of the patient

European journal of neurology, 2006-04, Vol.13 (4), p.427-428

2006

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Telomere length and mitochondrial DNA copy number in bipolar disorder: identification of a subgroup of young individuals with accelerated cellular aging

Signal Transduction through Prion Protein

Acute pain Factors predictive of post-operative pain and opioid requirement in multimodal analgesia following knee replacement

Amplification techniques and diagnosis of prion diseases

Genetic susceptibility and transmission factors in scrapie: detailed analysis of an epidemic in a closed flock of Romanov

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease mimicking nonconvulsive status epilepticus

A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion

Long-standing Prion Dementia Manifesting as Posterior Cortical Atrophy

Functional expression of p-glycoprotein and multidrug resistance-associated protein (mrp1) in primary cultures of rat astrocytes

Telomere length and mitochondrial DNA copy number in bipolar disorder: A sibling study

Compassionate use of quinacrine in Creutzfeldt-Jakob disease fails to show significant effects

Variant or sporadic Creutzfeldt-Jakob disease?

A novel mutation (G114V) in the prion protein gene in a family with inherited prion disease

Alzheimer's disease cerebro-spinal fluid biomarkers: A clinical research tool sometimes useful in daily clinical practice of memory clinics for the diagnosis of complex cases

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes

Diagnosis of Creutzfeldt-Jakob disease: effect of clinical criteria on incidence estimates

Antidepressant-induced mania, rapid cycling and the serotonin transporter gene polymorphism

Diagnosis associated with Tau higher than 1200 pg/mL: Insights from the clinical and laboratory practice

Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders

Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression

Fatal familial insomnia presenting as psychosis in an 18-year-old man

14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

Diagnostic value of CSF 14-3-3 detection in sporadic CJD diagnosis according to the age of the patient

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