UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 974

Sortiert nach

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

CNS neuroscience & therapeutics, 2021-10, Vol.27 (10), p.1146-1156

2021

Volltextzugriff (PDF)

Establishment of Rapid Detection Methods for rs76971248 Related to Leukemia

Disease markers, 2022, Vol.2022, p.9847708-8

2022

Volltextzugriff (PDF)

Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype Correlation

Frontiers in aging neuroscience, 2022-04, Vol.14, p.848919-848919

2022

Volltextzugriff (PDF)

Demographic Factors Among HIV Confirmed Blood Donors from 2013 to 2021 in Shenzhen

International journal of general medicine, 2023-01, Vol.16, p.425-434

2023

Volltextzugriff (PDF)

Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders

Clinical neurology and neurosurgery, 2019-02, Vol.177, p.92-96

2019

Volltextzugriff (PDF)

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings

Movement disorders, 2009-10, Vol.24 (13), p.2007-2011

2009

Volltextzugriff (PDF)

Robust adaptive control of a class of nonlinear systems with unknown dead-zone

Automatica (Oxford), 2004-03, Vol.40 (3), p.407-413

2004

Volltextzugriff (PDF)

Correlation of Human Leukocyte Antigen-E Genomic Polymorphism with Leukemia and Functional Study of Human Leukocyte Antigen-E Different Type Promoters

DNA and cell biology, 2022-02, Vol.41 (2), p.235

2022

Volltextzugriff (PDF)

Analysis of thermally induced machine tool errors of a crank press

Proceedings of the Institution of Mechanical Engineers. Part B, Journal of engineering manufacture, 2012-09, Vol.226 (9), p.1465-1478

2012

Volltextzugriff (PDF)

Clinical significance of HLA-E genotype and surface/soluble expression levels between healthy individuals and patients with acute leukemia

Leukemia & lymphoma, 2019-01, Vol.60 (1), p.208-215

2019

Volltextzugriff (PDF)

Analysis on clinical phenotype and gene mutation of progressive myoclonic epilepsy: one case report

Zhongguo xian dai shen jing ji bing za zhi, 2018-04, Vol.18 (4), p.272-277

2018

Volltextzugriff (PDF)

Efficacy and safety of cyclophosphamide as a sequential immunotherapy drug for anti-N-methyl-D-aspartate receptor encephalitis in children

Zhongguo dang dai er ke za zhi, 2017-06, Vol.19 (6), p.668-671

2017

Volltextzugriff (PDF)

A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis

Neurogenetics, 2011-02, Vol.12 (1), p.93-95

2011

Volltextzugriff (PDF)

Studies of Synergism/Antagonism for Lowering Interfacial Tensions in Alkyl Benzene Sulfonate Mixtures

Journal of dispersion science and technology, 2009-08, Vol.30 (7), p.1015-1019

2009

Volltextzugriff (PDF)

Design and Analysis of Curvature Adaptive Wall Climbing Robot

2021 IEEE Far East NDT New Technology & Application Forum (FENDT), 2021, p.177-184

2021

Volltextzugriff (PDF)

Adaptive sliding inverse control of a class of non-linear systems preceded by unknown non-symmetrical dead-zone

International journal of systems science, 2006-08, Vol.37 (10), p.699-708

2006

Volltextzugriff (PDF)

Surface Defect Detection of Cable Based on Threshold Image Difference

2021 IEEE Far East NDT New Technology & Application Forum (FENDT), 2021, p.185-190

2021

Volltextzugriff (PDF)

Design of Human-Machine Cooperative Control Algorithm for Lower Extremity Exoskeleton

2022 28th International Conference on Mechatronics and Machine Vision in Practice (M2VIP), 2022, p.1-6

2022

Volltextzugriff (PDF)

Novel omnidirectional climbing robot with adjustable magnetic adsorption mechanism

2016 23rd International Conference on Mechatronics and Machine Vision in Practice (M2VIP), 2016, p.1-5

2016

Volltextzugriff (PDF)

Design of Inspection Robot for Spherical Tank Based on Mecanum Wheel

2019 Far East NDT New Technology & Application Forum (FENDT), 2019, p.218-224

2019

Volltextzugriff (PDF)

Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome

Zhong hua yi xue za zhi, 2009-12, Vol.89 (47), p.3320-3323

2009

Volltextzugriff (PDF)

Existing Weld Seam Recognition Based on Image Processing

2017 Far East NDT New Technology & Application Forum (FENDT), 2017, p.181-186

2017

Volltextzugriff (PDF)

FTO-dependent demethylation of N6-methyladenosine regulates mRNA splicing and is required for adipogenesis

Cell research, 2014-12, Vol.24 (12), p.1403-1419

2014

Volltextzugriff (PDF)

Bilateral Laser Vision Tracking Synchronous Inspection Robotic System

2017 Far East NDT New Technology & Application Forum (FENDT), 2017, p.207-215

2017

Volltextzugriff (PDF)

Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

Zhong nan da xue xue bao. Journal of Central South University. Yi xue ban, 2006-10, Vol.31 (5), p.702-705

2006

Volltextzugriff (PDF)

1 – 25 von 974

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(799)
Mit Volltextzugriff
(873)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(10)

Menü

Weitere Dienste

Einstellungen

CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia

Establishment of Rapid Detection Methods for rs76971248 Related to Leukemia

Novel PANK2 Mutations in Patients With Pantothenate Kinase-Associated Neurodegeneration and the Genotype-Phenotype Correlation

Demographic Factors Among HIV Confirmed Blood Donors from 2013 to 2021 in Shenzhen

Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings

Robust adaptive control of a class of nonlinear systems with unknown dead-zone

Correlation of Human Leukocyte Antigen-E Genomic Polymorphism with Leukemia and Functional Study of Human Leukocyte Antigen-E Different Type Promoters

Analysis of thermally induced machine tool errors of a crank press

Clinical significance of HLA-E genotype and surface/soluble expression levels between healthy individuals and patients with acute leukemia

Analysis on clinical phenotype and gene mutation of progressive myoclonic epilepsy: one case report

Efficacy and safety of cyclophosphamide as a sequential immunotherapy drug for anti-N-methyl-D-aspartate receptor encephalitis in children

A novel CLN2/TPP1 mutation in a Chinese patient with late infantile neuronal ceroid lipofuscinosis

Studies of Synergism/Antagonism for Lowering Interfacial Tensions in Alkyl Benzene Sulfonate Mixtures

Design and Analysis of Curvature Adaptive Wall Climbing Robot

Adaptive sliding inverse control of a class of non-linear systems preceded by unknown non-symmetrical dead-zone

Surface Defect Detection of Cable Based on Threshold Image Difference

Design of Human-Machine Cooperative Control Algorithm for Lower Extremity Exoskeleton

Novel omnidirectional climbing robot with adjustable magnetic adsorption mechanism

Design of Inspection Robot for Spherical Tank Based on Mecanum Wheel

Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome

Existing Weld Seam Recognition Based on Image Processing

FTO-dependent demethylation of N6-methyladenosine regulates mRNA splicing and is required for adipogenesis

Bilateral Laser Vision Tracking Synchronous Inspection Robotic System

Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

Suchergebnisse filtern