P. Crino

发表

Developmental lineage of cell types in cortical dysplasia with balloon cells.

E. Aronica, E. Hol, Phillip Lamparello, 2007, Brain : a journal of neurology.

Internexin, MAP1B, and nestin in cortical dysplasia as markers of developmental maturity

J. Trojanowski, P. Crino, J. Eberwine, 1997, Acta Neuropathologica.

mTOR cascade activation distinguishes tubers from focal cortical dysplasia

E. Aronica, M. Baybis, P. Crino, 2004, Annals of neurology.

Homozygous boricua TBCK mutation causes neurodegeneration and aberrant autophagy

P. Crino, D. Wallace, C. Bönnemann, 2018, Annals of neurology.

Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment

J. D. Mills, L. Lagae, P. V. van Rijen, 2017, Scientific Reports.

A multilayered approach to studying cortical malformations

J. Detre, P. Crino, 2005, Neurology.

Reorganization of cingulate cortex in Alzheimer's disease: neuron loss, neuritic plaques, and muscarinic receptor binding.

B. Vogt, P. Crino, L. Vogt, 1992, Cerebral cortex.

Seizures in Acute Neurological Disorders

P. Crino, 2002 .

Focal Cortical Dysplasia

P. Crino, 2014, Seminars in Neurology.

Genetics of epilepsy: epilepsy research foundation workshop report.

J. H. Cross, Michael R. Johnson, I. Scheffer, 2007, Epileptic disorders : international epilepsy journal with videotape.

Involvement of free radicals in dementia of the Alzheimer type: A hypothesis

P. Crino, L. Volicer, 1990, Neurobiology of Aging.

E. Aronica, P. Crino, 2014, Neurotherapeutics.

Systemic and neurologic autoimmune disorders associated with seizures or epilepsy

P. Crino, A. Vincent, A. Vincent, 2011, Epilepsia.

Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia.

H. Hakonarson, P. Crino, M. Hegde, 2016, American journal of human genetics.

β-Amyloid Peptide and Amyloid Precursor Proteins in Olfactory Mucosa of Patients with Alzheimer's Disease, Parkinson's Disease, and down Syndrome

John A. Martin, J. Trojanowski, V. Lee, 1995 .

Genetics of tuberous sclerosis complex : implications for clinical practice

P. Crino, Daphne M. Hasbani, C. Caban, 2016 .

Tuberous sclerosis complex: genetic basis and management strategies

P. Crino, Victoria Tsai, 2012 .

Molecular Pathogenesis of Tuber Formation in Tuberous Sclerosis Complex

P. Crino, 2004, Journal of child neurology.

Expression profiling in tuberous sclerosis complex (TSC) knockout mouse astrocytes to characterize human TSC brain pathology

P. Crino, D. Gutmann, J. Declue, 2004, Glia.

Knockout of a Tuberous Sclerosis Gene Highlights Role of Glia in Epileptogenesis

P. Crino, 2003, Epilepsy currents.

Bourneville and Taylor: A developing story?

P. Crino, 2002, Annals of neurology.

Gene expression analysis as a strategy to understand the molecular pathogenesis of infantile spasms.

P. Crino, 2002, International review of neurobiology.

Impaired Reelin-Dab1 Signaling Contributes to Neuronal Migration Deficits of Tuberous Sclerosis Complex.

Seonhee Kim, P. Crino, M. Gambello, 2015, Cell reports.

The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission 1

Maria Thom, François Dubeau, Philippe Kahane, 2011, Epilepsia.

Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR

P. Lockhart, P. Crino, W. Maixner, 2015, Neurology.

Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy model

P. Crino, D. Gutmann, S. Mennerick, 2003, Annals of neurology.

Tuberous sclerosis complex: Developmental perspectives in psychiatry

P. Crino, 2000 .

Human Brain Malformations : From Genetics to Therapeutics Organized by

P. Crino, M. Sahin, 2015 .

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.

N W Wood, F Andermann, S M Sisodiya, 2001, Human molecular genetics.

Increased serotonin efflux by a partially oxidized serotonin: tryptamine-4,5-dione.

P. Crino, L. Volicer, J. C. Chen, 1989, The Journal of pharmacology and experimental therapeutics.

Multimodal Analysis of STRADA Function in Brain Development

Seonhee Kim, M. Baybis, P. Crino, 2020, Frontiers in Cellular Neuroscience.

Mouse and cellular models of KPTN-related disorder implicate mTOR signalling in cognitive and progressive overgrowth phenotypes

M. Hurles, C. Lelliott, B. Yalcin, 2022, bioRxiv.

STRADA‐mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiation

P. Crino, J. Parent, F. Majolo, 2021, Developmental neurobiology.

Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73

M. Hurles, E. Puffenberger, K. Strauss, 2015, Brain : a journal of neurology.

Molecular Characterization of the Dendritic Growth Cone: Regulated mRNA Transport and Local Protein Synthesis

P. Crino, J. Eberwine, 1996, Neuron.

GATORopathies: The role of amino acid regulatory gene mutations in epilepsy and cortical malformations

P. Crino, A. Bordey, Vincent J. Carson, 2019, Epilepsia.

New insights into the pathogenesis and prevention of tuberous sclerosis-associated neuropsychiatric disorders

P. Crino, 2019 .

New insights into the pathogenesis and prevention of tuberous

P. Crino, 2018 .

DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons

P. Lockhart, M. Baybis, P. Crino, 2018, Neurobiology of Disease.

Renal angiomyolipoma: long-term results after arterial embolization.

P. Crino, S. Stavropoulos, R. Shlansky-Goldberg, 2005, Journal of vascular and interventional radiology : JVIR.

Differential Expression of GABA and Glutamate‐receptor Subunits and Enzymes Involved in GABA Metabolism between Electrophysiologically Identified Hippocampal CA1 Pyramidal Cells and Interneurons

M. Baybis, P. Crino, M. Dichter, 2003, Epilepsia.

Dynamic analysis of 4E-BP1 phosphorylation in neurons with Tsc2 or Depdc5 knockout

M. Baybis, P. Crino, Philip H. Iffland, 2020, Experimental Neurology.

Magnetic resonance imaging of the cauda equina in Guillain‐Barré syndrome

P. Crino, R. Zimmerman, E. Raps, 1994, Neurology.

Magnetic resonsance imaging of the cauda equina in chronic inflammatory demyelination polyneuropathy

P. Crino, R. Grossman, A. Rostami, 1993 .

Renal cell carcinomatous meningitis

P. Crino, M. Sperling, C. Katsetos, 1995, Neurology.

NPRL3: Direct Effects on Human Phenotypic Variability, mTOR Signaling, Subcellular mTOR Localization, Cortical Lamination, and Seizure Susceptibility

E. Puffenberger, M. Baybis, P. Crino, 2020, bioRxiv.

Neurodevelopment in Seizure‐prone and Seizure‐resistant Rat Strains: Recognizing Conflicts in Management

P. Crino, D. Mcintyre, K. Gilby, 2007, Epilepsia.

Renal angiomyolipoma: long-term results after arterial embolization.

P. Crino, S. Stavropoulos, R. Shlansky-Goldberg, 2005, Journal of vascular and interventional radiology : JVIR.

Functional expression of the seven-transmembrane HIV-1 co-receptor APJ in neural cells.

P. Crino, D. Kolson, E. Lavi, 2000, Journal of neurovirology.

Ezrin, radixin, and moesin are components of Schwann cell microvilli

P. Crino, D. Gutmann, S. Scherer, 2001, Journal of neuroscience research.

Embolization of giant renal angiomyolipomas: technique and results.

P. Crino, S. Stavropoulos, S. Trerotola, 2010, Journal of vascular and interventional radiology : JVIR.

Functional expression of the seven-transmembrane

P. Crino, D. Kolson, E. Lavi, 2000 .

Sending Mixed Signals: The Expanding Role of Molecular Cascade Mutations in Malformations of Cortical Development and Epilepsy

P. Crino, Philip H. Iffland, 2016, Epilepsy currents.

Laminar alterations in gamma-aminobutyric acidA, muscarinic, and beta adrenoceptors and neuron degeneration in cingulate cortex in Alzheimer's disease.

B. Vogt, P. Crino, L. Volicer, 1991, Journal of neurochemistry.

Reply: HPV in focal cortical dysplasia

P. Crino, 2015, Annals of neurology.

The TARC/sICAM5 Ratio in Patient Plasma is a Candidate Biomarker for Drug Resistant Epilepsy

P. Crino, J. Pollard, O. Eidelman, 2013, Front. Neur..

The tuberous sclerosis complex.

P. Crino, K. Nathanson, E. Henske, 2006, The New England journal of medicine.

Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex

E. Aronica, K. Boer, P. Crino, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

Attention and sentence processing deficits in Parkinson's disease: the role of anterior cingulate cortex.

M. Reivich, M. Grossman, P. Crino, 1992, Cerebral cortex.

mTOR and epileptogenesis in developmental brain malformations

P. Crino, M. Wong, Peter B. Crino, 2010 .

Biallelic TSC gene inactivation in tuberous sclerosis complex

E. Aronica, P. Crino, K. Nathanson, 2010, Neurology.

Co-expression of cyclin D1 and phosphorylated ribosomal S6 proteins in hemimegalencephaly

E. Aronica, K. Boer, M. Baybis, 2007, Acta Neuropathologica.

Differential Cellular Gene Expression in Ganglioglioma

E. Aronica, P. Crino, U. Samadani, 2007, Epilepsia.

Focal brain malformations: a spectrum of disorders along the mTOR cascade.

P. Crino, 2007, Novartis Foundation symposium.

Differential expression of glutamate and GABA-A receptor subunit mRNA in cortical dysplasia

P. Crino, G. Baltuch, A. Duhaime, 2001, Neurology.

Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells of cortical tubers

B. Scheithauer, P. Crino, R. White, 2001, Annals of neurology.

Mechanistic target of rapamycin (mTOR) signaling in status epilepticus

P. Crino, 2019, Epilepsy & Behavior.

Monoaminergic Innervation of Cingulate Cortex

Patrick R. Hof, John H. Morrison, J. Morrison, 1993 .

Mechanisms of epileptogenicity in cortical dysplasias

T. Babb, G. Mathern, P. Crino, 2004, Neurology.

Novel Histopathological Patterns in Cortical Tubers of Epilepsy Surgery Patients with Tuberous Sclerosis Complex

Pavel Krsek, Thomas Czech, Daniela Prayer, 2016, PloS one.

Sequestration of RNA in Alzheimer's disease neurofibrillary tangles and senile plaques

J. Trojanowski, V. Lee, P. Crino, 1997, Annals of neurology.

Review : Single-Cell mRNA Amplification: Implications for Basic and Clinical Neuroscience

P. Crino, J. Eberwine, M. Dichter, 1995 .

A neuropathological study of two autopsy cases of syndromic hemimegalencephaly

E. Aronica, K. Boer, P. Crino, 2007, Neuropathology and applied neurobiology.

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene

F. Woermann, P. Canoll, I. Blumcke, 2022, Neurology.

Clinicopathologic study of paraneoplastic brainstem encephalitis and ophthalmoparesis.

P. Crino, S. Galetta, E. Raps, 1996, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Postoperative epilepsy in patients undergoing craniotomy for glioblastoma multiforme.

P. Crino, K. Judy, M. Philips, 2001, Journal of experimental & clinical cancer research : CR.

Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly

A. Allen, P. Crino, C. Hulette, 2017, Cold Spring Harbor molecular case studies.

The mTOR signalling cascade: paving new roads to cure neurological disease

P. Crino, 2016, Nature Reviews Neurology.

mTOR signaling in epilepsy: insights from malformations of cortical development.

P. Crino, 2015, Cold Spring Harbor perspectives in medicine.

Molecular Pathology of Alzheimer’s Disease and Related Disorders

J. Trojanowski, V. Lee, P. Crino, 1999 .

Somatic mutation involving diverse genes leads to a spectrum of focal cortical malformations

G. Mckhann, P. Canoll, P. Crino, 2021, medRxiv.

Early Progenitor Cell Marker Expression Distinguishes Type II From Type I Focal Cortical Dysplasias

K. Strauss, E. Aronica, S. Sisodiya, 2010, Journal of neuropathology and experimental neurology.

Refractory Nonlesional Neocortical Epilepsy: Current Trends

P. Crino, S. Tobochnik, C. Gutierrez, 2011 .

Tuberous sclerosis and epilepsy: Role of astrocytes

Michael Wong, P. Crino, M. Wong, 2012, Glia.

Rapamycin and tuberous sclerosis complex: From Easter Island to epilepsy

P. Crino, 2008, Annals of neurology.

Epileptogenesis and Reduced Inward Rectifier Potassium Current in Tuberous Sclerosis Complex‐1–Deficient Astrocytes

P. Crino, D. Gutmann, E. Uhlmann, 2005, Epilepsia.

E. Aronica, P. Crino, 2014, Neurotherapeutics.

Fetal Brain Lesions in Tuberous Sclerosis Complex: TORC1 Activation and Inflammation

E. Aronica, P. Crino, A. Prabowo, 2013, Brain pathology.

Cytoarchitectural alterations are widespread in cerebral cortex in tuberous sclerosis complex

Eleonora Aronica, E. Aronica, M. Baybis, 2012, Acta Neuropathologica.

Inflammation in epilepsy: Clinical observations

Eleonora Aronica, E. Aronica, P. Crino, 2011, Epilepsia.

Enhanced epidermal growth factor, hepatocyte growth factor, and vascular endothelial growth factor expression in tuberous sclerosis complex.

E. Aronica, M. Baybis, P. Crino, 2011, The American journal of pathology.

Gene Expression Analysis of Tuberous Sclerosis Complex Cortical Tubers Reveals Increased Expression of Adhesion and Inflammatory Factors

P. V. van Rijen, E. Aronica, K. Boer, 2009, Brain pathology.

Evolving neurobiology of tuberous sclerosis complex

P. Crino, 2013, Acta Neuropathologica.

Rapamycin Prevents Seizures After Depletion of STRADA in a Rare Neurodevelopmental Disorder

K. Strauss, M. Baybis, P. Crino, 2013, Science Translational Medicine.

Detection of human papillomavirus in human focal cortical dysplasia type IIB

Eleonora Aronica, Peter B Crino, Victoria Tsai, 2012, Annals of neurology.

Single cell lineage analysis in human focal cortical dysplasia.

P. Crino, Y. Hua, 2003, Cerebral cortex.

The tuberous sclerosis complex.

P. Crino, K. Nathanson, E. Henske, 2006, The New England journal of medicine.

Pathogenesis of TSC in the Brain

P. Crino, H. Vinters, Rupal I. Mehta, 2010 .

Mutational Analysis of Cell Types in Tuberous Sclerosis Complex (TSC)

P. Crino, 2009 .

Mutational Analysis of Cell Types in TSC

P. Crino, 2008 .

The neurobiology of the tuberous sclerosis complex

P. Crino, Leah Marcotte, 2007, NeuroMolecular Medicine.

Fetal brain mTOR signaling activation in tuberous sclerosis complex.

E. Aronica, M. Baybis, P. Crino, 2014, Cerebral cortex.

Focal malformations of cortical development: New vistas for molecular pathogenesis

P. Crino, K. Lim, 2013, Neuroscience.

mTOR: A pathogenic signaling pathway in developmental brain malformations.

P. Crino, 2011, Trends in molecular medicine.

Deletion of 15q11.2–15q13.1 in isolated human hemimegalencephaly

E. Aronica, M. Baybis, P. Crino, 2009, Acta Neuropathologica.

Focal brain malformations: Seizures, signaling, sequencing

P. Crino, 2009, Epilepsia.

Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex

E. Aronica, K. Boer, P. Crino, 2008, Epilepsy Research.

Targeted Gene Expression Analysis in Hemimegalencephaly: Activation of β‐Catenin Signaling

E. Aronica, M. Baybis, P. Crino, 2005, Brain pathology.

Molecular Pathogenesis of Focal Cortical Dysplasia and Hemimegalencephaly

P. Crino, 2004, Journal of child neurology.

Altered Expression of Neurotransmitter‐receptor Subunit and Uptake Site mRNAs in Hemimegalencephaly

E. Aronica, M. Baybis, P. Crino, 2004, Epilepsia.

Markers of cellular proliferation are expressed in cortical tubers

B. Scheithauer, M. Baybis, P. Crino, 2003, Annals of neurology.

Embryonic neuronal markers in tuberous sclerosis: single-cell molecular pathology.

J. Trojanowski, P. Crino, J. Eberwine, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Expression of ICAM-1, TNF-alpha, NF kappa B, and MAP kinase in tubers of the tuberous sclerosis complex.

M. Baybis, P. Crino, G. McKhann, 2003, Neurobiology of disease.

New developments in the neurobiology of the tuberous sclerosis complex.

P. Crino, E. Henske, E P Henske, 1999, Neurology.

STRADalpha deficiency results in aberrant mTORC1 signaling during corticogenesis in humans and mice.

K. Strauss, M. Baybis, P. Crino, 2010, The Journal of clinical investigation.

Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.

Peter B Crino, David A Ramsay, David W Craig, 2007, Brain : a journal of neurology.

The role of somatic mutational events in the pathogenesis of epilepsy

P. Crino, Philip H. Iffland, 2019, Current opinion in neurology.

Tsc2 Null Murine Neuroepithelial Cells Are a Model for Human Tuber Giant Cells, and Show Activation of an mTOR Pathway

Hongbing Zhang, P. Crino, H. Onda, 2002, Molecular and Cellular Neuroscience.

Magnetic resonance imaging of the cauda equina in chronic inflammatory demyelinating polyneuropathy.

P. Crino, R. Grossman, A. Rostami, 1993, Annals of neurology.

Predominance of neuronal mRNAs in individual Alzheimer's disease senile plaques

J. Weingarten, J. Trojanowski, V. Lee, 1999, Annals of neurology.

Viral expression of constitutively active AKT3 induces CST axonal sprouting and regeneration, but also promotes seizures

P. Crino, George M. Smith, Jie Chen, 2021, Experimental Neurology.

Familial cortical dysplasia caused by mutation in the mammalian target of rapamycin regulator NPRL3

P. Lockhart, P. Crino, M. Bahlo, 2015, Annals of neurology.

Simian immunodeficiency virus encephalitis: analysis of envelope sequences from individual brain multinucleated giant cells and tissue samples.

P. Crino, A. Lackner, S. Westmoreland, 2002, Virology.

Cellular and molecular basis of cerebral dysgenesis

P. Crino, James Eberwine, 1997, Journal of neuroscience research.

Stimulation of glutamate receptor protein synthesis and membrane insertion within isolated neuronal dendrites.

P. Crino, J. Eberwine, J. E. Kacharmina, 2000, Proceedings of the National Academy of Sciences of the United States of America.

BK channel properties correlate with neurobehavioral severity in three KCNMA1-linked channelopathy mouse models

P. Crino, Abby G. Lieberman, S. M. Park, 2022, bioRxiv.

Preparation of cDNA from single cells and subcellular regions.

P. Crino, J. Eberwine, J. E. Kacharmina, 1999, Methods in enzymology.

Machado‐Joseph disease gene product is a cytoplasmic protein widely expressed in brain

K. Fischbeck, H. Paulson, P. Crino, 1997, Annals of neurology.

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy

C. Schevon, A. Allen, G. Mckhann, 2018, Annals of neurology.

Increased Expression of the Neuronal Glutamate Transporter (EAAT3/EAAC1) in Hippocampal and Neocortical Epilepsy

P. Crino, D. Coulter, A. Brooks-Kayal, 2002, Epilepsia.

Tuberous sclerosis complex.

P. Crino, Daphne M. Hasbani, 2018, Handbook of clinical neurology.

Malformations of Cortical Development

P. Crino, G. Heuer, 2011 .

Malformations of cortical development: molecular pathogenesis and experimental strategies.

P. Crino, 2004, Advances in experimental medicine and biology.

Neurodevelopmental Disorders as a Cause of Seizures: Neuropathologic, Genetic, and Mechanistic Considerations

P. Crino, H. Vinters, H. Miyata, 2002, Brain pathology.

Reelin’ in Genes for Cortical Dysplasia

P. Crino, 2001, Epilepsy currents.

Giant cell astrocytomas in tuberous sclerosis complex.

P. Crino, P. D. de Vries, D. Franz, 2009, Archives of disease in childhood.

Ganglioglioma, mTOR Activation, and Epileptogenesis

P. Crino, Jelte Helferrich, 2012 .

Transcription of intermediate filament genes is enhanced in focal cortical dysplasia

P. Crino, G. Baltuch, P. Taylor, 2001, Acta Neuropathologica.

mTOR pathway inhibition prevents neuroinflammation and neuronal death in a mouse model of cerebral palsy

M. Baybis, P. Crino, Tanya S Ferguson, 2016, Neurobiology of Disease.

Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal period

J. D. Mills, L. Lagae, P. V. van Rijen, 2022, Journal of neurodevelopmental disorders.

Beta-Amyloid peptide and amyloid precursor proteins in olfactory mucosa of patients with Alzheimer's disease, Parkinson's disease, and Down syndrome.

J. Trojanowski, V. Lee, P. Crino, 1995, The Annals of otology, rhinology, and laryngology.

Brain gangliosides in dementia of the Alzheimer type.

B. Vogt, P. Crino, E. Bird, 1989, Archives of neurology.

Expression of ICAM-1, TNF-α, NFκB, and MAP kinase in tubers of the tuberous sclerosis complex

M. Baybis, P. Crino, G. McKhann, 2003, Neurobiology of Disease.

mTORopathies: A Road Well-Traveled

P. Crino, 2020, Epilepsy currents.

Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

P. Lockhart, I. Scheffer, G. Jackson, 2015, Annals of clinical and translational neurology.

Focal Cortical Dysplasia: Gene Mutations, Cell Signaling, and Therapeutic Implications.

P. Crino, Philip H. Iffland, 2017, Annual review of pathology.

Association of Epileptic and Nonepileptic Seizures and Changes in Circulating Plasma Proteins Linked to Neuroinflammation

J. Pollard, P. Crino, John M. Gledhill, 2021, Neurology.

The Tuberous Sclerosis Complex: Clinical Manifestations And Molecular Genetics

J. Pollard, P. Crino, 2005 .

Traumatic Brain Injury Alters the Molecular Fingerprint of TUNEL-Positive Cortical Neurons In Vivo: A Single-Cell Analysis

P. Crino, J. Eberwine, R. Raghupathi, 2000, The Journal of Neuroscience.

Gene Expression, Genetics, and Genomics in Epilepsy: Some Answers, More Questions

P. Crino, 2007, Epilepsia.

Epilepsy and cortical dysplasias

Kelvin Chou, P. Crino, K. Chou, 2000, Current treatment options in neurology.

Molecular Pathogenesis of Focal Cortical Dysplasia and Hemimegalencephaly

P. Crino, 2004 .

Cellular localization of serotonin 1A, 1B and uptake sites in cingulate cortex of the rat.

B. Vogt, P. Crino, L. Volicer, 1990, The Journal of pharmacology and experimental therapeutics.

MicroRNA‐34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis

J. D. Mills, L. Lagae, P. V. van Rijen, 2020, Neuropathology and applied neurobiology.

Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment

J. D. Mills, L. Lagae, P. V. van Rijen, 2017, Scientific Reports.

Dysregulation of PINCH signaling in mesial temporal epilepsy

C. Heck, P. Crino, D. Langford, 2017, Journal of Clinical Neuroscience.

Laminar Alterations in γ‐Aminobutyric AcidA, Muscarinic, and β Adrenoceptors and Neuron Degeneration in Cingulate Cortex in Alzheimer's Disease

B. Vogt, P. Crino, L. Volicer, 1991 .

Presence and phosphorylation of transcription factors in developing dendrites.

K. Becker, P. Crino, J. Eberwine, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Laminar distributions of muscarinic acetylcholine, serotonin, GABA and opioid receptors in human posterior cingulate cortex

B. Vogt, P. Crino, E. Bird, 1990, Neuroscience.

Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility

I. Scheffer, G. Jackson, P. Crino, 2014, Epilepsia.

Neurotoxic effects of partially oxidized serotonin: tryptamine-4,5-dione

B. Vogt, P. Crino, L. Volicer, 1989, Brain Research.

Epileptogenic but MRI-normal perituberal tissue in Tuberous Sclerosis Complex contains tuber-specific abnormalities

P. Crino, H. Weiner, G. McKhann, 2015, Acta neuropathologica communications.

Give PEAF a Chance

Peter B Crino, P. Crino, 2005, Epilepsy currents.

Gene Profiling in Temporal Lobe Epilepsy Tissue and Dysplastic Lesions

P. Crino, A. Becker, Peter B. Crino, 2006, Epilepsia.

Differential cellular expression of neurotrophins in cortical tubers of the tuberous sclerosis complex.

B. Scheithauer, M. Baybis, P. Crino, 2001, The American journal of pathology.

Analysis of mRNA Populations from Single Live and Fixed Cells of the Central Nervous System

P. Crino, J. Eberwine, 1997, Current protocols in neuroscience.

Vascularization in mTOR Mouse Mutants: An Effort Not in Vein

P. Crino, Soad Elziny, 2023, eNeuro.

Molecular Pathology of Alzheimer’s Disease and Related Disorders

J. Trojanowski, V. Lee, P. Crino, 1999 .

Mild TSC Phenotype and Non-Penetrance Associated with a Frameshift Variant in TSC2 Prompts Caution in Evaluating Pathogenicity of Frameshift Variants.

R. Ekong, P. Crino, M. Nellist, 2023, Gene.

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.

G. Mckhann, P. Canoll, P. Crino, 2022, Brain : a journal of neurology.

Effects of rapamycin on gene expression, morphology, and electrophysiological properties of rat hippocampal neurons

P. Crino, M. Dichter, S. Rüegg, 2007, Epilepsy Research.

NPRL3 loss alters neuronal morphology, mTOR localization, cortical lamination, and seizure threshold.

E. Puffenberger, P. Crino, J. Babus, 2022, Brain : a journal of neurology.

Tuberous sclerosis complex

P. Crino, R. Nass, 2008, Neurology.

Do We Have a Cure for Tuberous Sclerosis Complex?

P. Crino, 2008, Epilepsy currents.

Gene expression in TUNEL-positive neurons in human immunodeficiency virus-infected brain

P. Crino, D. Kolson, P. Sabnekar, 2011, Journal of NeuroVirology.

Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes

M. Hurles, C. Lelliott, B. Yalcin, 2023, Brain : a journal of neurology.

The tuberous sclerosis complex

P. Crino, Ksenia A. Orlova, 2010, Annals of the New York Academy of Sciences.

Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia.

H. Hakonarson, P. Crino, M. Hegde, 2016, American journal of human genetics.

Detection of human papillomavirus in human focal cortical dysplasia type IIB

E. Aronica, P. Crino, Whitney E. Parker, 2012, Annals of neurology.