Lista de obras - Nobuo Sanjo - Dominio Público Uruguay

A controlled inflammation and a regulatory immune system are associated with more favorable prognosis of progressive multifocal leukoencephalopathy

scientific article published on 03 December 2018

APH-1 interacts with mature and immature forms of presenilins and nicastrin and may play a role in maturation of presenilin.nicastrin complexes

artículo científico publicado en 2003

Ambulatory Gait Behavior in Patients With Dementia: A Comparison With Parkinson's Disease.

artículo científico publicado en 2015

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene

artículo científico publicado en 2018

Both the sequence and length of the C terminus of PEN-2 are critical for intermolecular interactions and function of presenilin complexes

artículo científico publicado en 2004

Brainstem congestion due to carotid-cavernous fistula via a shunt from the external carotid artery

artículo científico publicado en 2011

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

artículo científico publicado en 2014

Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's Disease

artículo científico publicado en 2019

Delayed leukoencephalopathy after carbon monoxide poisoning presenting as subacute dementia.

artículo científico publicado en 2014

Depressive disorder may be associated with raphe nuclei lesions in patients with brainstem infarction

artículo científico publicado en 2017

Descriptive epidemiology of prion disease in Japan: 1999-2012.

artículo científico publicado en 2014

Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay

artículo científico publicado en 2013

Elevated platelet microparticle levels after acute ischemic stroke with concurrent idiopathic thrombocytopenic purpura

artículo científico publicado en 2013

Failure of mefloquine therapy in progressive multifocal leukoencephalopathy: report of two Japanese patients without human immunodeficiency virus infection

artículo científico publicado en 2012

Focal sharp waves are a specific early-stage marker of the MM2-cortical form of sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2020

Graft-related disease progression in dura mater graft-associated Creutzfeldt-Jakob disease: a cross-sectional study

artículo científico publicado en 2013

Hereditary neuropathy with liability to pressure palsy combined with suspected schwannomas of the peroneal and radial nerves

scientific article published on 27 October 2011

Increased expression of neuronal apolipoprotein E in human brain with cerebral infarction.

artículo científico publicado en 2003

Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan.

artículo científico publicado en 2013

Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related gamma-secretase

artículo científico publicado en 2010

MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type

scientific article published on 24 August 2020

Malignant lymphoma presented as left trigeminal neuralgia

artículo científico publicado en 2009

Methotrexate-associated lymphoproliferative disorder in a patient with neuromyelitis optica spectrum disorder: An implication for pathogenesis mediated by Epstein-Barr virus

artículo científico publicado en 2017

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study

artículo científico publicado en 2012

Myasthenia Gravis Complicated with Peripheral T-cell Lymphoma, Not Otherwise Specified (PTCL-NOS), Following Thymectomy and Longstanding Tacrolimus Therapy.

artículo científico publicado en 2017

Presenilin 1 and presenilin 2 have differential effects on the stability and maturation of nicastrin in Mammalian brain

scientific journal article

Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress

artículo científico publicado en 2010

Prion disease--the characteristics and diagnostic points in Japan

artículo científico publicado en 2010

Progressive Multifocal Leukoencephalopathy with Balanced CD4/CD8 T-Cell Infiltration and Good Response to Mefloquine Treatment.

artículo científico publicado en 2016

Progressive Multifocal Leukoencephalopathy with Inflammatory Reactions

artículo científico publicado en 2016

Prospective 10-year surveillance of human prion diseases in Japan.

artículo científico publicado en 2010

Quantifying prion disease penetrance using large population control cohorts

artículo científico publicado en 2016

Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.

artículo científico publicado en 2013

Safety of tapering tacrolimus dose in patients with well-controlled anti-acetylcholine receptor antibody-positive myasthenia gravis

artículo científico publicado en 2019

Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene

artículo científico publicado en 2014

Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy.

artículo científico publicado en 2016

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene

article

TMP21 is a presenilin complex component that modulates gamma-secretase but not epsilon-secretase activity

artículo científico publicado en 2006

Tacrolimus monotherapy: a promising option for ocular myasthenia gravis.

artículo científico publicado en 2013

The presenilin proteins are components of multiple membrane-bound complexes that have different biological activities

artículo científico publicado en 2004

Transient abundance of presenilin 1 fragments/nicastrin complex associated with synaptogenesis during development in rat cerebellum

artículo científico publicado en 2005

Visual reproduction on the Wechsler Memory Scale-Revised as a predictor of Alzheimer's disease in Japanese patients with mild cognitive impairments.

artículo científico publicado en 2013

Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations

artículo científico publicado en 2005

[Rapid progressive HTLV-1-associated myelopathy with bronchoalveolar lesions and a long spinal cord lesion extending to almost the entire spinal cord].

artículo científico publicado en 2011

[Review of basic knowledge, surveillance and infectious control of prion disease].

artículo científico publicado en 2013

Lista de obras de Nobuo Sanjo

A controlled inflammation and a regulatory immune system are associated with more favorable prognosis of progressive multifocal leukoencephalopathy

APH-1 interacts with mature and immature forms of presenilins and nicastrin and may play a role in maturation of presenilin.nicastrin complexes

Ambulatory Gait Behavior in Patients With Dementia: A Comparison With Parkinson's Disease.

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene

Both the sequence and length of the C terminus of PEN-2 are critical for intermolecular interactions and function of presenilin complexes

Brainstem congestion due to carotid-cavernous fistula via a shunt from the external carotid artery

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's Disease

Delayed leukoencephalopathy after carbon monoxide poisoning presenting as subacute dementia.

Depressive disorder may be associated with raphe nuclei lesions in patients with brainstem infarction

Descriptive epidemiology of prion disease in Japan: 1999-2012.

Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay

Elevated platelet microparticle levels after acute ischemic stroke with concurrent idiopathic thrombocytopenic purpura

Failure of mefloquine therapy in progressive multifocal leukoencephalopathy: report of two Japanese patients without human immunodeficiency virus infection

Focal sharp waves are a specific early-stage marker of the MM2-cortical form of sporadic Creutzfeldt-Jakob disease

Graft-related disease progression in dura mater graft-associated Creutzfeldt-Jakob disease: a cross-sectional study

Hereditary neuropathy with liability to pressure palsy combined with suspected schwannomas of the peroneal and radial nerves

Increased expression of neuronal apolipoprotein E in human brain with cerebral infarction.

Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan.

Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related gamma-secretase

MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type

Malignant lymphoma presented as left trigeminal neuralgia

Methotrexate-associated lymphoproliferative disorder in a patient with neuromyelitis optica spectrum disorder: An implication for pathogenesis mediated by Epstein-Barr virus

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study

Myasthenia Gravis Complicated with Peripheral T-cell Lymphoma, Not Otherwise Specified (PTCL-NOS), Following Thymectomy and Longstanding Tacrolimus Therapy.

Presenilin 1 and presenilin 2 have differential effects on the stability and maturation of nicastrin in Mammalian brain

Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress

Prion disease--the characteristics and diagnostic points in Japan

Progressive Multifocal Leukoencephalopathy with Balanced CD4/CD8 T-Cell Infiltration and Good Response to Mefloquine Treatment.

Progressive Multifocal Leukoencephalopathy with Inflammatory Reactions

Prospective 10-year surveillance of human prion diseases in Japan.

Quantifying prion disease penetrance using large population control cohorts

Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases.

Safety of tapering tacrolimus dose in patients with well-controlled anti-acetylcholine receptor antibody-positive myasthenia gravis

Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene

Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy.

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene

TMP21 is a presenilin complex component that modulates gamma-secretase but not epsilon-secretase activity

Tacrolimus monotherapy: a promising option for ocular myasthenia gravis.

The presenilin proteins are components of multiple membrane-bound complexes that have different biological activities

Transient abundance of presenilin 1 fragments/nicastrin complex associated with synaptogenesis during development in rat cerebellum

Visual reproduction on the Wechsler Memory Scale-Revised as a predictor of Alzheimer's disease in Japanese patients with mild cognitive impairments.

Wild-type PINK1 prevents basal and induced neuronal apoptosis, a protective effect abrogated by Parkinson disease-related mutations

[Rapid progressive HTLV-1-associated myelopathy with bronchoalveolar lesions and a long spinal cord lesion extending to almost the entire spinal cord].

[Review of basic knowledge, surveillance and infectious control of prion disease].