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...

PHENOTYPE-GUIDED GENETIC TESTING OF PEDIATRIC INHERITED RETINAL DISEASE IN THE UNITED ARAB EMIRATES

Retina (Philadelphia, Pa.), 2020-09, Vol.40 (9), p.1829-1837

Khan, Arif O.

2020

Volltextzugriff (PDF)

Review and qualitative analysis of submodule-level distributed power electronic solutions in PV power systems

Renewable & sustainable energy reviews, 2017-09, Vol.76, p.516-528

2017

Volltextzugriff (PDF)

Rumpel Leede Sign

Mayo Clinic proceedings, 2022-07, Vol.97 (7), p.1230-1231

2022

Volltextzugriff (PDF)

In Reply—Rumpel-Leede Sign: Consider Underlying Vitamin C Deficiency

Mayo Clinic proceedings, 2022-11, Vol.97 (11), p.2164-2165

2022

Volltextzugriff (PDF)

Revised Recommendations of the Consortium of MS Centers Task Force for a Standardized MRI Protocol and Clinical Guidelines for the Diagnosis and Follow-Up of Multiple Sclerosis

American journal of neuroradiology : AJNR, 2016-03, Vol.37 (3), p.394-401

2016

Volltextzugriff (PDF)

Narrowing the Expertise Gap for Predicting Intracranial Aneurysm Hemodynamics: Impact of Solver Numerics versus Mesh and Time-Step Resolution

American journal of neuroradiology : AJNR, 2015-07, Vol.36 (7), p.1310-1316

2015

Volltextzugriff (PDF)

Evaluation of the magnitude and location of Cam deformity using three dimensional CT analysis

The bone & joint journal, 2014-09, Vol.96-B (9), p.1167-1171

2014

Volltextzugriff (PDF)

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

Genome research, 2013-02, Vol.23 (2), p.236-247

2013

Volltextzugriff (PDF)

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

PloS one, 2015-09, Vol.10 (9), p.e0137973-e0137973

2015

Volltextzugriff (PDF)

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

PloS one, 2016-11, Vol.11 (11), p.e0162620-e0162620

2016

Volltextzugriff (PDF)

Hierarchical and non-hierarchical mineralisation of collagen

Biomaterials, 2011-02, Vol.32 (5), p.1291-1300

2011

Volltextzugriff (PDF)

Topological data analysis quantifies biological nano-structure from single molecule localization microscopy

Bioinformatics, 2020-03, Vol.36 (5), p.1614-1621

2020

Volltextzugriff (PDF)

ADAMTS18 -related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome

Taiwan journal of ophthalmology, 2023-10, Vol.13 (4), p.540-542

Khan, Arif O

2023

Volltextzugriff (PDF)

Typical Forms of Plans for Certain Investigative (Search) Actions

Вісник Харківського національного університету внутрішніх справ, 2020-06, Vol.89 (2), p.271-283

Khan, O. O.

2020

Volltextzugriff (PDF)

Mechanisms of action of disease-modifying agents and brain volume changes in multiple sclerosis

Neurology, 2008-07, Vol.71 (2), p.136-144

2008

Volltextzugriff (PDF)

Fundus autofluorescence imaging in hereditary retinal diseases

Acta ophthalmologica (Oxford, England), 2018-08, Vol.96 (5), p.e549-e561

2018

Volltextzugriff (PDF)

Perspectives for Using the Programmatic Approach within the Activities of Law Enforcement Agencies of Ukraine

Вісник Харківського національного університету внутрішніх справ, 2019-12, Vol.87 (4), p.170-178

Khan, O. O.

2019

Volltextzugriff (PDF)

Methodology fundamentals for investigating violations of the laws and customs of war

Вісник Харківського національного університету внутрішніх справ, 2023-07, Vol.101 (2 (P. 1)), p.301-309

2023

Volltextzugriff (PDF)

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Nature communications, 2016-04, Vol.7 (1), p.10953-10953, Article 10953

2016

Volltextzugriff (PDF)

Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

American journal of human genetics, 2014-05, Vol.94 (5), p.755-759

2014

Volltextzugriff (PDF)

Super-resolution imaging and quantification of megakaryocytes and platelets

Platelets (Edinburgh), 2020-07, Vol.31 (5), p.559-569

2020

Volltextzugriff (PDF)

Low-dose Btk inhibitors selectively block platelet activation by CLEC-2

Haematologica (Roma), 2021-01, Vol.106 (1), p.208-219

2021

Volltextzugriff (PDF)

Severity of SARS-CoV-2 infection is associated with high numbers of alveolar mast cells and their degranulation

Frontiers in immunology, 2022-09, Vol.13, p.968981-968981

2022

Volltextzugriff (PDF)

Anterior segment dysgenesis: Insights into the genetics and pathogenesis

Indian journal of ophthalmology, 2022-07, Vol.70 (7), p.2293-2303

2022

Volltextzugriff (PDF)

Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function

Haematologica (Roma), 2022-01, Vol.107 (1), p.243-259

2022

Volltextzugriff (PDF)

1 – 25 von 8.679

Suche als RSS-Feed

Aktive Filter

SpracheItalienisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(7.197)
Mit Volltextzugriff
(7.050)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

10 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(4.536)
Life Sciences & Biomedicine
(2.833)
Humans
(1.879)
Physical Sciences
(1.286)
Female
(1.069)
Male
(1.016)
Physics
(938)
Technology
(813)
Biological And Medical Sciences
(640)
Adult
(583)
Middle Aged
(541)
Medical Sciences
(501)
Animals
(438)
Engineering
(420)
Aged
(383)
Chemistry
(382)
Surgery
(328)
Ophthalmology
(316)
Child
(285)
Adolescent
(280)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

EZB Free E-Journals
(3.978)
Ingenta
(3.379)
MEDLINE
(2.289)
Elsevier ScienceDirect Journals Complete
(1.773)
Journals@Ovid Full Text
(1.765)
IngentaConnect Journals
(1.701)
Publisher or Other Site
(1.225)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(1.089)
Springer journals
(905)
Wiley Online Library
(691)
American Physical Society Journals
(489)
Wiley Online Library Full Collection 2018
(420)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(341)
IEEE Electronic Library (IEL)
(318)
American Physical Society [PROLA]
(297)
Taylor & Francis:Master (3349 titles)
(286)
Taylor & Francis Journals Auto-Holdings Collection
(285)
Ebook Central Perpetual and DDA
(274)
Taylor & Francis Current Content Access
(273)
eBooks on EBSCOhost
(266)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

PHENOTYPE-GUIDED GENETIC TESTING OF PEDIATRIC INHERITED RETINAL DISEASE IN THE UNITED ARAB EMIRATES

Review and qualitative analysis of submodule-level distributed power electronic solutions in PV power systems

Rumpel Leede Sign

In Reply—Rumpel-Leede Sign: Consider Underlying Vitamin C Deficiency

Revised Recommendations of the Consortium of MS Centers Task Force for a Standardized MRI Protocol and Clinical Guidelines for the Diagnosis and Follow-Up of Multiple Sclerosis

Narrowing the Expertise Gap for Predicting Intracranial Aneurysm Hemodynamics: Impact of Solver Numerics versus Mesh and Time-Step Resolution

Evaluation of the magnitude and location of Cam deformity using three dimensional CT analysis

Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes

Missense Mutations in CRYAB Are Liable for Recessive Congenital Cataracts

Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts

Hierarchical and non-hierarchical mineralisation of collagen

Topological data analysis quantifies biological nano-structure from single molecule localization microscopy

ADAMTS18 -related anterior segment dysgenesis mistaken as Axenfeld-Rieger syndrome

Typical Forms of Plans for Certain Investigative (Search) Actions

Mechanisms of action of disease-modifying agents and brain volume changes in multiple sclerosis

Fundus autofluorescence imaging in hereditary retinal diseases

Perspectives for Using the Programmatic Approach within the Activities of Law Enforcement Agencies of Ukraine

Methodology fundamentals for investigating violations of the laws and customs of war

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Mutations in ASPH Cause Facial Dysmorphism, Lens Dislocation, Anterior-Segment Abnormalities, and Spontaneous Filtering Blebs, or Traboulsi Syndrome

Super-resolution imaging and quantification of megakaryocytes and platelets

Low-dose Btk inhibitors selectively block platelet activation by CLEC-2

Severity of SARS-CoV-2 infection is associated with high numbers of alveolar mast cells and their degranulation

Anterior segment dysgenesis: Insights into the genetics and pathogenesis

Post-translational polymodification of β1-tubulin regulates motor protein localisation in platelet production and function

Aktive Filter

Suchergebnisse filtern