UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Ataxias in Brazil

Arquivos de neuro-psiquiatria, 2024-08, Vol.82 (8), p.1-2

Tsuji, Shoji

2024

Volltextzugriff (PDF)

Significance of hyponatremia in Kawasaki disease

Pediatrics international, 2020-03, Vol.62 (3), p.307-307

Tsuji, Shoji

2020

Volltextzugriff (PDF)

The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

Movement disorders, 2022-06, Vol.37 (6), p.1131-1148

2022

Volltextzugriff (PDF)

The long and winding road to the etiology of idiopathic nephrotic syndrome in children: Focusing on abnormalities in the gut microbiota

Pediatrics international, 2021-09, Vol.63 (9), p.1011-1019

2021

Volltextzugriff (PDF)

Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorder

Journal of human genetics, 2023-03, Vol.68 (3), p.169-174

2023

Volltextzugriff (PDF)

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Nature genetics, 2019-08, Vol.51 (8), p.1222-1232

2019

Volltextzugriff (PDF)

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy

Nature genetics, 2018-04, Vol.50 (4), p.581-590

2018

Volltextzugriff (PDF)

Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons

Neurobiology of disease, 2012-03, Vol.45 (3), p.1121-1128

2012

Volltextzugriff (PDF)

Brainstem Encephalitis with Lesions Spreading along Neuroaxonal Fibers

Internal Medicine, 2024/07/01, Vol.63(13), pp.1965-1966

2024

Volltextzugriff (PDF)

CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease

PloS one, 2010-11, Vol.5 (11), p.e15522

2010

Volltextzugriff (PDF)

Genomic aspects of sporadic neurodegenerative diseases

Biochemical and biophysical research communications, 2014-09, Vol.452 (2), p.221-225

2014

Volltextzugriff (PDF)

Adrenoleukodystrophy siblings with a novel ABCD1 missense variant presenting with phenotypic differences: a case report and literature review

Journal of human genetics, 2021-05, Vol.66 (5), p.535-537

2021

Volltextzugriff (PDF)

Our Evolving Understanding of Kawasaki Disease Pathogenesis: Role of the Gut Microbiota

Frontiers in immunology, 2020-07, Vol.11, p.1616-1616

2020

Volltextzugriff (PDF)

Dysbiosis in Gut Microbiota in Children Born Preterm Who Developed Autism Spectrum Disorder: A Pilot Study

Journal of autism and developmental disorders, 2023-10, Vol.53 (10), p.4012-4020

2023

Volltextzugriff (PDF)

Idiopathic nephrotic syndrome in children: role of regulatory T cells and gut microbiota

Pediatric research, 2021-04, Vol.89 (5), p.1185-1191

2021

Volltextzugriff (PDF)

Human genetic variation database, a reference database of genetic variations in the Japanese population

Journal of human genetics, 2016-06, Vol.61 (6), p.547-553

2016

Volltextzugriff (PDF)

COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population

Journal of the neurological sciences, 2021-10, Vol.429, p.117623-117623, Article 117623

2021

Volltextzugriff (PDF)

Paraneoplastic Cerebellar Degeneration Leading to an Early Diagnosis of Peritoneal Serous Papillary Carcinoma

Internal Medicine, 2024/10/01, Vol.63(19), pp.2679-2682

2024

Volltextzugriff (PDF)

The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force

Cerebellum (London, England), 2019-12, Vol.18 (6), p.1098-1125

2019

Volltextzugriff (PDF)

Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population

Journal of human genetics, 2021-03, Vol.66 (3), p.237-241

2021

Volltextzugriff (PDF)

Nocturnal enuresis and poor sleep quality

Pediatrics international, 2018-11, Vol.60 (11), p.1020-1023

2018

Volltextzugriff (PDF)

Broadening Neurologic Manifestations in Adult Patients With Dravet Syndrome

Neurology, 2022-05, Vol.98 (22), p.913-914

Tsuji, Shoji

2022

Volltextzugriff (PDF)

Neuron-specific methylome analysis reveals epigenetic regulation and tau-related dysfunction of BRCA1 in Alzheimer’s disease

Proceedings of the National Academy of Sciences - PNAS, 2017-11, Vol.114 (45), p.E9645-E9654

2017

Volltextzugriff (PDF)

Chédiak-Higashi syndrome presenting as a hereditary spastic paraplegia

Journal of human genetics, 2022-02, Vol.67 (2), p.119-121

2022

Volltextzugriff (PDF)

Increased facilitation of the primary motor cortex in de novo Parkinson's disease

Parkinsonism & related disorders, 2019-09, Vol.66, p.125-129

2019

Volltextzugriff (PDF)

1 – 25 von 1.478

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.209)
Mit Volltextzugriff
(1.215)

Publikationsform

Sprache

Englisch
(1.305)
Japanisch
(213)
Koreanisch
(1)
Russisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(764)
Ingenta
(629)
EZB Electronic Journals Library
(613)
Journals@Ovid Ovid Full Text
(487)
Elsevier ScienceDirect Journals Complete
(289)
Wiley-Blackwell Journals
(273)
Publisher or Other Site
(262)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(213)
Wiley Online Library Full Collection 2018
(184)
IngentaConnect Journals
(181)
SpringerNature Journals
(151)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(124)
Nature
(76)
Oxford journals
(58)
Taylor & Francis
(33)
Taylor & Francis Online
(32)
Nexis Uni
(32)
Oxford Journals 2020 Medicine
(30)
Taylor & Francis Journals
(27)
JSTOR
(16)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Neurology
(50)
Internal Medicine
(38)
Journal Of The Neurological Sciences
(38)
Rinshō Shinkeigaku
(38)
Annals Of Neurology
(36)
Journal Of Human Genetics
(33)
Alzheimer's & Dementia
(31)
Neurology And Clinical Neuroscience
(31)
Clinical Neurophysiology
(24)
Archives Of Neurology
(23)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Ataxias in Brazil

Significance of hyponatremia in Kawasaki disease

The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

The long and winding road to the etiology of idiopathic nephrotic syndrome in children: Focusing on abnormalities in the gut microbiota

Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorder

Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy

Profound downregulation of the RNA editing enzyme ADAR2 in ALS spinal motor neurons

Brainstem Encephalitis with Lesions Spreading along Neuroaxonal Fibers

CpG demethylation enhances alpha-synuclein expression and affects the pathogenesis of Parkinson's disease

Genomic aspects of sporadic neurodegenerative diseases

Adrenoleukodystrophy siblings with a novel ABCD1 missense variant presenting with phenotypic differences: a case report and literature review

Our Evolving Understanding of Kawasaki Disease Pathogenesis: Role of the Gut Microbiota

Dysbiosis in Gut Microbiota in Children Born Preterm Who Developed Autism Spectrum Disorder: A Pilot Study

Idiopathic nephrotic syndrome in children: role of regulatory T cells and gut microbiota

Human genetic variation database, a reference database of genetic variations in the Japanese population

COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population

Paraneoplastic Cerebellar Degeneration Leading to an Early Diagnosis of Peritoneal Serous Papillary Carcinoma

The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force

Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population

Nocturnal enuresis and poor sleep quality

Broadening Neurologic Manifestations in Adult Patients With Dravet Syndrome

Neuron-specific methylome analysis reveals epigenetic regulation and tau-related dysfunction of BRCA1 in Alzheimer’s disease

Chédiak-Higashi syndrome presenting as a hereditary spastic paraplegia

Increased facilitation of the primary motor cortex in de novo Parkinson's disease

Suchergebnisse filtern