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...

Efficiency of a therapeutic patient education programme in children with severe atopic dermatitis

Journal of the European Academy of Dermatology and Venereology, 2020-10, Vol.34 (10), p.e648-e651

2020

Volltextzugriff (PDF)

Risk factors for corticophobia in atopic dermatitis

Journal of the European Academy of Dermatology and Venereology, 2020-12, Vol.34 (12), p.e846-e849

2020

Volltextzugriff (PDF)

Development and co-construction of a therapeutic patient education program for albinism

Annales de dermatologie et de vénéréologie, 2021-12, Vol.148 (4), p.246-250

2021

Volltextzugriff (PDF)

Iminosugars: from synthesis to therapeutic applications

1st ed., 2007

Volltextzugriff (PDF)

Delphi-Based Expert Consensus Statements for the Management of Percutaneous Radiofrequency Neurotomy in the Treatment of Lumbar Facet Joint Syndrome

Pain and therapy, 2023-06, Vol.12 (3), p.863-877

2023

Volltextzugriff (PDF)

Correction to: Delphi-Based Expert Consensus Statements for the Management of Percutaneous Radiofrequency Neurotomy in the Treatment of Lumbar Facet Joint Syndrome

Pain and therapy, 2023-10, Vol.12 (5), p.1307-1308

2023

Volltextzugriff (PDF)

X Chromosome-Linked Kallmann Syndrome: Stop Mutations Validate the Candidate Gene

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (17), p.8190-8194

1992

Volltextzugriff (PDF)

Facteurs de risque de corticophobie au cours de la dermatite atopique

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A97-A98

2020

Volltextzugriff (PDF)

Primary Angiitis of the Central Nervous System: Description of the First Fifty‐Two Adults Enrolled in the French Cohort of Patients With Primary Vasculitis of the Central Nervous System

Arthritis & rheumatology (Hoboken, N.J.), 2014-05, Vol.66 (5), p.1315-1326

2014

Volltextzugriff (PDF)

Co-construction d’un programme d’éducation thérapeutique dédié à l’albinisme

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A272-A273

2020

Volltextzugriff (PDF)

Impact d’une formation e-learning sur les compétences des pharmaciens dans la prise en charge de l’eczéma atopique : l’expérience POP Training

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A243-A243

2020

Volltextzugriff (PDF)

Les ateliers de l’atopie : analyse d’une activité monocentrique et perspectives

Annales de dermatologie et de vénéréologie, 2017-12, Vol.144 (12), p.S80-S80

2017

Volltextzugriff (PDF)

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Nature genetics, 1997-02, Vol.15 (2), p.157-164

1997

Volltextzugriff (PDF)

Estimation of National Colorectal-Cancer Incidence Using Claims Databases

Journal of Cancer Epidemiology, 2012-01, Vol.2012 (2012), p.55-61

2012

Volltextzugriff (PDF)

Development and validation of a liquid chromatographic/tandem mass spectrometric assay for the quantitation of nucleoside HIV reverse transcriptase inhibitors in biological matrices

Journal of mass spectrometry., 2005-01, Vol.40 (1), p.9-18

2005

Volltextzugriff (PDF)

Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.422-425

1996

Volltextzugriff (PDF)

Effect of Cell Cycle Arrest on the Activity of Nucleoside Analogues against Human Immunodeficiency Virus Type 1

Journal of Virology, 2005-12, Vol.79 (23), p.14815-14821

2005

Volltextzugriff (PDF)

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Cell, 1991-10, Vol.67 (2), p.423-435

1991

Volltextzugriff (PDF)

Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1

Human molecular genetics, 1997-12, Vol.6 (13), p.2247-2255

1997

Volltextzugriff (PDF)

X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome

European journal of endocrinology, 2016-03, Vol.174 (3), p.281-288

2016

Volltextzugriff (PDF)

Development of an assay method for the detection and quantification of protease and non-nucleoside reverse transcriptase inhibitors in plasma and in peripherical blood mononuclear cells by liquid chromatography coupled with ultraviolet or tandem mass spectrometry detection

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2005-05, Vol.819 (1), p.47-57

2005

Volltextzugriff (PDF)

Multicentre randomised controlled trial to investigate usefulness of the rapid diagnostic βLACTA test performed directly on bacterial cell pellets from respiratory, urinary or blood samples for the early de-escalation of carbapenems in septic intensive care unit patients: the BLUE-CarbA protocol

BMJ open, 2019-02, Vol.9 (2), p.e024561-e024561

2019

Volltextzugriff (PDF)

Construction of a Yeast Artificial Chromosome Contig Spanning the Pseudoautosomal Region and Isolation of 25 New Sequence-Tagged Sites

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.691-697

1993

Volltextzugriff (PDF)

BOR and BO Syndromes Are Allelic Defects of EYA1

European journal of human genetics : EJHG, 1997-07, Vol.5 (4), p.242-246

1997

Volltextzugriff (PDF)

1 – 25 von 555

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(429)
Mit Volltextzugriff
(495)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Efficiency of a therapeutic patient education programme in children with severe atopic dermatitis

Risk factors for corticophobia in atopic dermatitis

Development and co-construction of a therapeutic patient education program for albinism

Iminosugars: from synthesis to therapeutic applications

Delphi-Based Expert Consensus Statements for the Management of Percutaneous Radiofrequency Neurotomy in the Treatment of Lumbar Facet Joint Syndrome

Correction to: Delphi-Based Expert Consensus Statements for the Management of Percutaneous Radiofrequency Neurotomy in the Treatment of Lumbar Facet Joint Syndrome

X Chromosome-Linked Kallmann Syndrome: Stop Mutations Validate the Candidate Gene

Facteurs de risque de corticophobie au cours de la dermatite atopique

Primary Angiitis of the Central Nervous System: Description of the First Fifty‐Two Adults Enrolled in the French Cohort of Patients With Primary Vasculitis of the Central Nervous System

Co-construction d’un programme d’éducation thérapeutique dédié à l’albinisme

Impact d’une formation e-learning sur les compétences des pharmaciens dans la prise en charge de l’eczéma atopique : l’expérience POP Training

Les ateliers de l’atopie : analyse d’une activité monocentrique et perspectives

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Estimation of National Colorectal-Cancer Incidence Using Claims Databases

Conservation-restauration de l’architecture du mouvement moderne

Development and validation of a liquid chromatographic/tandem mass spectrometric assay for the quantitation of nucleoside HIV reverse transcriptase inhibitors in biological matrices

Characterization of a Translocation-Associated Deletion Defines the Candidate Region for the Gene Responsible for Branchio-Oto-Renal Syndrome

Effect of Cell Cycle Arrest on the Activity of Nucleoside Analogues against Human Immunodeficiency Virus Type 1

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Clustering of Mutations Responsible for Branchio-Oto-Renal (BOR) Syndrome in the Eyes Absent Homologous Region (eyaHR) of EYA1

X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome

Development of an assay method for the detection and quantification of protease and non-nucleoside reverse transcriptase inhibitors in plasma and in peripherical blood mononuclear cells by liquid chromatography coupled with ultraviolet or tandem mass spectrometry detection

Multicentre randomised controlled trial to investigate usefulness of the rapid diagnostic βLACTA test performed directly on bacterial cell pellets from respiratory, urinary or blood samples for the early de-escalation of carbapenems in septic intensive care unit patients: the BLUE-CarbA protocol

Construction of a Yeast Artificial Chromosome Contig Spanning the Pseudoautosomal Region and Isolation of 25 New Sequence-Tagged Sites

BOR and BO Syndromes Are Allelic Defects of EYA1

Suchergebnisse filtern