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...

Synaptopathology Involved in Autism Spectrum Disorder

Frontiers in cellular neuroscience, 2018-12, Vol.12, p.470-470

2018

Volltextzugriff (PDF)

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes

Frontiers in neuroscience, 2019-04, Vol.13, p.349-349

2019

Volltextzugriff (PDF)

A study of the impact damages detection and dynamic responses of RC bridge piers based on a frequency domain correlation method

Advances in mechanical engineering, 2023-03, Vol.15 (3), p.168781322311518

2023

Volltextzugriff (PDF)

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient

BMC medical genetics, 2020-11, Vol.21 (1), p.235-235, Article 235

2020

Volltextzugriff (PDF)

Ketogenic Diet as a Treatment for Super-Refractory Status Epilepticus in Febrile Infection-Related Epilepsy Syndrome

Frontiers in neurology, 2019-04, Vol.10, p.423-423

2019

Volltextzugriff (PDF)

Central nervous system infection with Seoul Orthohantavirus in a child after hematopoietic stem cell transplantation: a case report

Virology journal, 2022-04, Vol.19 (1), p.75-75, Article 75

2022

Volltextzugriff (PDF)

Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients

BMC medical genomics, 2021-07, Vol.14 (1), p.182-9, Article 182

2021

Volltextzugriff (PDF)

Protein kinase C-α signals P115RhoGEF phosphorylation and RhoA activation in TNF-α-induced mouse brain microvascular endothelial cell barrier dysfunction

Journal of neuroinflammation, 2011-04, Vol.8 (1), p.28-28, Article 28

2011

Volltextzugriff (PDF)

Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1 -Related Neurodevelopmental Disorder

Frontiers in pediatrics, 2022-01, Vol.9, p.755344-755344

2022

Volltextzugriff (PDF)

Role of p115RhoGEF in lipopolysaccharide-induced mouse brain microvascular endothelial barrier dysfunction

Brain research, 2011-04, Vol.1387, p.1-7

2011

Volltextzugriff (PDF)

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children

Frontiers in molecular biosciences, 2021-12, Vol.8, p.792319-792319

2021

Volltextzugriff (PDF)

Albumin Therapy Enhances Collateral Perfusion after Laser-Induced Middle Cerebral Artery Branch Occlusion: A Laser Speckle Contrast Flow Study

Journal of cerebral blood flow and metabolism, 2012-11, Vol.32 (11), p.2012-2022

2012

Volltextzugriff (PDF)

The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak

Frontiers in pediatrics, 2020-08, Vol.8, p.495-495

2020

Volltextzugriff (PDF)

Gold nanocluster embedded bovine serum albumin nanofibers-graphene hybrid membranes for the efficient detection and separation of mercury ion

Chemical engineering journal (Lausanne, Switzerland : 1996), 2018-03, Vol.335, p.176-184

2018

Volltextzugriff (PDF)

Screening and identification of dynamin-1 interacting proteins in rat brain synaptosomes

Brain research, 2014-01, Vol.1543, p.17-27

2014

Volltextzugriff (PDF)

Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort

Clinica chimica acta, 2022-01, Vol.524, p.179-186

2022

Volltextzugriff (PDF)

Clinical characteristics of acute glomerulonephritis with presentation of nephrotic syndrome at onset in children

International immunopharmacology, 2020-09, Vol.86, p.106724-106724, Article 106724

2020

Volltextzugriff (PDF)

Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders

Gene, 2024-03, Vol.897, p.148071-148071, Article 148071

2024

Volltextzugriff (PDF)

A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel

Clinica chimica acta, 2022-05, Vol.530, p.74-80

2022

Volltextzugriff (PDF)

Clinical and radiological features, treatment responses and prognosis in pediatric patients with co-existing anti-N-methyl-D-aspartate receptor and myelin oligodendrocyte glycoprotein antibody-associated encephalitis: A single center study

Multiple sclerosis and related disorders, 2024-01, Vol.81, p.105133-105133, Article 105133

2024

Volltextzugriff (PDF)

De novo variants of DEAF1 cause intellectual disability in six Chinese patients

Clinica chimica acta, 2021-07, Vol.518, p.17-21

2021

Volltextzugriff (PDF)

The role of ubiquitin/Nedd4-2 in the pathogenesis of mesial temporal lobe epilepsy

Physiology & behavior, 2015-05, Vol.143, p.104-112

2015

Volltextzugriff (PDF)

Construction Site Inspection System Based on Panoramic Image Cloud Processing Technology

Multimedia Technology and Enhanced Learning, p.285-298

Volltextzugriff (PDF)

Micro-blog topic recommendation based on knowledge flow and user selection

Journal of computational science, 2018-05, Vol.26, p.512-521

2018

Volltextzugriff (PDF)

Effectiveness and Safety of Different Once-Daily Doses of Adrenocorticotropic Hormone for Infantile Spasms

Paediatric drugs, 2017-08, Vol.19 (4), p.357-365

2017

Volltextzugriff (PDF)

1 – 25 von 258

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(199)
Mit Volltextzugriff
(226)

Publikationsform

Sprache

Englisch
(251)
Chinesisch
(8)

Erscheinungsjahr

n.n

Thema

Science & Technology
(181)
Life Sciences & Biomedicine
(126)
Humans
(62)
Male
(37)
Animals
(36)
Technology
(31)
Physical Sciences
(29)
Female
(26)
Science & Technology - Other Topics
(21)
Mice
(19)
Multidisciplinary Sciences
(17)
Engineering
(16)
Environmental Sciences & Ecology
(16)
Oncology
(16)
Environmental Sciences
(15)
Child
(14)
Meta-Analysis
(14)
Patients
(14)
Proteins
(14)
Neurosciences & Neurology
(13)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(16)
... seit 30 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Synaptopathology Involved in Autism Spectrum Disorder

Neurological Diseases With Autism Spectrum Disorder: Role of ASD Risk Genes

A study of the impact damages detection and dynamic responses of RC bridge piers based on a frequency domain correlation method

First case report of cerebral folate deficiency caused by a novel mutation of FOLR1 gene in a Chinese patient

Ketogenic Diet as a Treatment for Super-Refractory Status Epilepticus in Febrile Infection-Related Epilepsy Syndrome

Central nervous system infection with Seoul Orthohantavirus in a child after hematopoietic stem cell transplantation: a case report

Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patients

Protein kinase C-α signals P115RhoGEF phosphorylation and RhoA activation in TNF-α-induced mouse brain microvascular endothelial cell barrier dysfunction

Correlation Analyses of Clinical Manifestations and Variant Effects in KCNB1 -Related Neurodevelopmental Disorder

Role of p115RhoGEF in lipopolysaccharide-induced mouse brain microvascular endothelial barrier dysfunction

Urine Organic Acids as Metabolic Indicators for Global Developmental Delay/Intellectual Disability in Chinese Children

Albumin Therapy Enhances Collateral Perfusion after Laser-Induced Middle Cerebral Artery Branch Occlusion: A Laser Speckle Contrast Flow Study

The Recommendations for the Management of Chinese Children With Epilepsy During the COVID-19 Outbreak

Gold nanocluster embedded bovine serum albumin nanofibers-graphene hybrid membranes for the efficient detection and separation of mercury ion

Screening and identification of dynamin-1 interacting proteins in rat brain synaptosomes

Autism spectrum disorder and comorbid neurodevelopmental disorders (ASD-NDDs): Clinical and genetic profile of a pediatric cohort

Clinical characteristics of acute glomerulonephritis with presentation of nephrotic syndrome at onset in children

Targeted sequencing identifies risk variants in 202 candidate genes for neurodevelopmental disorders

A novel KCNQ2 missense variant in non-syndromic intellectual disability causes mild gain-of-function of Kv7.2 channel

Clinical and radiological features, treatment responses and prognosis in pediatric patients with co-existing anti-N-methyl-D-aspartate receptor and myelin oligodendrocyte glycoprotein antibody-associated encephalitis: A single center study

De novo variants of DEAF1 cause intellectual disability in six Chinese patients

The role of ubiquitin/Nedd4-2 in the pathogenesis of mesial temporal lobe epilepsy

Construction Site Inspection System Based on Panoramic Image Cloud Processing Technology

Micro-blog topic recommendation based on knowledge flow and user selection

Effectiveness and Safety of Different Once-Daily Doses of Adrenocorticotropic Hormone for Infantile Spasms

Suchergebnisse filtern