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Deep Brain Stimulation for OCD in a Patient With Comorbidities: Epilepsy, Tics, Autism, and Major Depressive Disorder

The journal of neuropsychiatry and clinical neurosciences, 2021-05, Vol.33 (2), p.167-171

2021

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Postsurgical morbidity and mortality favorably informs deep brain stimulation for new indications including schizophrenia and schizoaffective disorder

Frontiers in surgery, 2023-03, Vol.10, p.958452-958452

2023

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Pathobiology of human cerebrovascular malformations: basic mechanisms and clinical relevance

Neurosurgery, 2004-07, Vol.55 (1), p.1-17

2004

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Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the α7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

American journal of medical genetics, 2001-01, Vol.105 (1), p.20-22

2001

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Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7)

Genomics (San Diego, Calif.), 1998-09, Vol.52 (2), p.173-185

1998

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Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion

Stroke (1970), 2005-04, Vol.36 (4), p.872-874

2005

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A 2-base pair deletion polymorphism in the partial duplication of the alpha 7 nicotinic acetylcholine gene (CHRFAM7A) on chromosome 15q14 is associated with schizophrenia

Brain research, 2009-09, Vol.1291, p.1-11

2009

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Biology of vascular malformations of the brain

Stroke (1970), 2009-12, Vol.40 (12), p.e694-e702

2009

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A 2-base pair deletion polymorphism in the partial duplication of the α7 nicotinic acetylcholine gene ( CHRFAM7A ) on chromosome 15q14 is associated with schizophrenia

Brain research, 2009, Vol.1291, p.1-11

2009

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Cavernous Malformations of the Brain and Spinal Cord

1, 2011

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An adult case of leukoencephalopathy with intracranial calcifications and cysts

Neurology, 2006-11, Vol.67 (10), p.1890

2006

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Comparison of polymorphisms in the α7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-11, Vol.123B (1), p.39-49

2003

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Correlated expression analysis of genes implicated in schizophrenia: Identification of putative disease-related pathways

New Horizons in Translational Medicine, 2017-01, Vol.3 (5), p.224-232

2017

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Smoking and schizophrenia: abnormal nicotinic receptor expression

European journal of pharmacology, 2000-03, Vol.393 (1), p.237-242

2000

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Gene Modulation: Keep Your Eye on RNAi

Neurosurgery, 2003-04, Vol.52 (4)

2003

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Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts

Neurogenetics, 2008-02, Vol.9 (1), p.25-31

2008

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CEREBRAL CAVERNOUS MALFORMATIONS: SOMATIC MUTATIONS IN VASCULAR ENDOTHELIAL CELLS. Commentaries

Neurosurgery, 2009, Vol.65 (1), p.138-145

2009

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Spinal root arteriovenous malformations and same-segment cord cavernous malformation in familial cerebral cavernous malformation. Case report

Journal of neurosurgery. Spine, 2008-09, Vol.9 (3), p.249

2008

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Global translational medicine initiatives and programs

Translational biomedicine, 2011-01, Vol.2 (3)

2011

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Symptom dimensions in obsessive-compulsive disorder: Toward quantitative phenotypes

American journal of medical genetics, 2001-01, Vol.105 (1), p.28-30

2001

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Familial cerebral cavernous malformations: Rio de Janeiro study and review of the recommendations for management Malformação cavernosa cerebral familiar: um estudo no Rio de Janeiro e revisão das recomendações para tratamento

Arquivos de neuro-psiquiatria, 2008-12, Vol.66 (4), p.795-799

2008

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Spectrum of genotype and clinical manifestations in cerebral cavernous malformations. Commentary

Neurosurgery, 2006, Vol.59 (6), p.1278-1285

2006

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Elevated DISC1 transcript levels in PBMCs during acute psychosis in patients with schizophrenia

Translational biomedicine, 2011, Vol.2 (1)

2011

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What genes can teach us about human cerebrovascular malformations

Clinical neurosurgery, 2004, Vol.51, p.140

2004

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Deep Brain Stimulation for OCD in a Patient With Comorbidities: Epilepsy, Tics, Autism, and Major Depressive Disorder

Postsurgical morbidity and mortality favorably informs deep brain stimulation for new indications including schizophrenia and schizoaffective disorder

Pathobiology of human cerebrovascular malformations: basic mechanisms and clinical relevance

Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the α7-nicotinic acetylcholine receptor subunit gene (CHRNA7)

Genomic Organization and Partial Duplication of the Human α7 Neuronal Nicotinic Acetylcholine Receptor Gene (CHRNA7)

Biallelic somatic and germ line CCM1 truncating mutations in a cerebral cavernous malformation lesion

A 2-base pair deletion polymorphism in the partial duplication of the alpha 7 nicotinic acetylcholine gene (CHRFAM7A) on chromosome 15q14 is associated with schizophrenia

Biology of vascular malformations of the brain

A 2-base pair deletion polymorphism in the partial duplication of the α7 nicotinic acetylcholine gene ( CHRFAM7A ) on chromosome 15q14 is associated with schizophrenia

Cavernous Malformations of the Brain and Spinal Cord

An adult case of leukoencephalopathy with intracranial calcifications and cysts

Comparison of polymorphisms in the α7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects

Correlated expression analysis of genes implicated in schizophrenia: Identification of putative disease-related pathways

Smoking and schizophrenia: abnormal nicotinic receptor expression

Gene Modulation: Keep Your Eye on RNAi

Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts

CEREBRAL CAVERNOUS MALFORMATIONS: SOMATIC MUTATIONS IN VASCULAR ENDOTHELIAL CELLS. Commentaries

Spinal root arteriovenous malformations and same-segment cord cavernous malformation in familial cerebral cavernous malformation. Case report

Global translational medicine initiatives and programs

Cavernous Malformations of the Brain and Spinal Cord

Symptom dimensions in obsessive-compulsive disorder: Toward quantitative phenotypes

Familial cerebral cavernous malformations: Rio de Janeiro study and review of the recommendations for management Malformação cavernosa cerebral familiar: um estudo no Rio de Janeiro e revisão das recomendações para tratamento

Spectrum of genotype and clinical manifestations in cerebral cavernous malformations. Commentary

Elevated DISC1 transcript levels in PBMCs during acute psychosis in patients with schizophrenia

What genes can teach us about human cerebrovascular malformations

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