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...

Le syndrome de Dorfman–Chanarin à travers une étude de 15 cas tunisiens

Annales de dermatologie et de vénéréologie, 2018-12, Vol.145 (12), p.S258-S259

2018

Volltextzugriff (PDF)

Atteinte thyroïdienne dans le syndrome de Dorfman-Chanarin

Annales de dermatologie et de vénéréologie, 2018-12, Vol.145 (12), p.S69-S70

2018

Volltextzugriff (PDF)

Impact des eaux phréatiques sur la salinité et le rendement du palmier dattier à Ouargla

Algerian Journal of Arid Environment : Revue des Sciences de la Terre et de la Vie., 2012, Vol.2 (2), p.71-77

2012

Volltextzugriff (PDF)

Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families

Archives de l'Institut Pasteur de Tunis, 2006, Vol.83 (1-4), p.19

2006

Volltextzugriff (PDF)

Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene

Bioscience reports, 2010-12, Vol.30 (6), p.405-411

2010

Volltextzugriff (PDF)

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

Neurogenetics, 2004-02, Vol.5 (1), p.27-34

2004

Volltextzugriff (PDF)

Mutational analysis of the mitochondrial 12S rRNA and tRNA{sup Ser(UCN)} genes in Tunisian patients with nonsyndromic hearing loss

Biochemical and biophysical research communications, 2006-02, Vol.340 (4)

2006

Volltextzugriff (PDF)

Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies

Bioscience reports, 2011-04, Vol.31 (2), p.125-135

2011

Volltextzugriff (PDF)

Severe MDC1A congenital muscular dystrophy due to a splicing mutation in the LAMA2 gene resulting in exon skipping and significant decrease of mRNA level

Genetic testing, 2007-09, Vol.11 (3), p.199-207

2007

Volltextzugriff (PDF)

Mutational analysis of the mitochondrial 12S rRNA and tRNA super(S) super(e) super(r) super(() super(U) super(C) super(N) super()) genes in Tunisian patients with nonsyndromic hearing loss

Biochemical and biophysical research communications, 2006-02, Vol.340 (4), p.1251-1258

2006

Volltextzugriff (PDF)

Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role

Genetic testing, 2008-12, Vol.12 (4), p.581-586

2008

Volltextzugriff (PDF)

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients

Neuromuscular disorders : NMD, 2003, Vol.13 (1), p.4-12

2003

Volltextzugriff (PDF)

Are Islamic finance innovations enough for investors to escape from a financial downturn? Further evidence from portfolio simulations

Applied economics, 2013-08, Vol.45 (24), p.3412-3420

2013

Volltextzugriff (PDF)

Devenir des étudiants de troisième cycle de médecine générale de Saint-Étienne entre 2014 et 2020

EXERCER, 2023-11, Vol.34 (197), p.428-430

2023

Volltextzugriff (PDF)

Cu0-loaded SBA-15@ZnO with improved electrical properties and affinity towards hydrogen

Applied surface science, 2017, Vol.404, p.146-153

2017

Volltextzugriff (PDF)

Metal-organo-zinc oxide materials: Investigation on the structural, optical and electrical properties

Journal of alloys and compounds, 2016-01, Vol.656, p.146-153

2016

Volltextzugriff (PDF)

CAD/CAE integration: updating the CAD model after a FEM analysis

International journal of advanced manufacturing technology, 2015-01, Vol.76 (1-4), p.391-400

2015

Volltextzugriff (PDF)

A methodology for enhanced flexibility of integrated assessment in agriculture

Environmental science & policy, 2009-08, Vol.12 (5), p.546-561

2009

Volltextzugriff (PDF)

Retrieve reusable 3D CAD objects based on hidden Markov models (HMM)

2022 26th International Conference Information Visualisation (IV), 2022, p.451-456

2022

Volltextzugriff (PDF)

Electrochemical oxidation of succinic acid in aqueous solutions using boron doped diamond anodes

International journal of environmental science and technology (Tehran), 2012, Vol.9 (1), p.135-143

2012

Volltextzugriff (PDF)

Cu 0 -loaded SBA-15@ZnO with improved electrical properties and affinity towards hydrogen

Applied surface science, 2017-05, Vol.404, p.146-153

2017

Volltextzugriff (PDF)

Electrochemical degradation of an anionic surfactant on boron-doped diamond anodes

Journal of hazardous materials, 2008-10, Vol.158 (2), p.430-437

2008

Volltextzugriff (PDF)

Electrochemical Oxidation of Benzoic Acid Derivatives on Boron Doped Diamond: Voltammetric Study and Galvanostatic Electrolyses

Chemical engineering & technology, 2006-08, Vol.29 (8), p.944-950

2006

Volltextzugriff (PDF)

Proposition of a Geometric Complexity Model for Additive Manufacturing Process Based on CAD

2019 23rd International Conference Information Visualisation (IV), 2019, p.442-448

2019

Volltextzugriff (PDF)

Generic Bio-Economic Farm Model for Environmental and Economic Assessment of Agricultural Systems

Environmental management (New York), 2010-12, Vol.46 (6), p.862-877

2010

Volltextzugriff (PDF)

1 – 25 von 84

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(62)

Publikationsform

Sprache

Französisch
(43)
Englisch
(42)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Le syndrome de Dorfman–Chanarin à travers une étude de 15 cas tunisiens

Atteinte thyroïdienne dans le syndrome de Dorfman-Chanarin

Impact des eaux phréatiques sur la salinité et le rendement du palmier dattier à Ouargla

Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families

Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

Mutational analysis of the mitochondrial 12S rRNA and tRNA{sup Ser(UCN)} genes in Tunisian patients with nonsyndromic hearing loss

Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies

Severe MDC1A congenital muscular dystrophy due to a splicing mutation in the LAMA2 gene resulting in exon skipping and significant decrease of mRNA level

Mutational analysis of the mitochondrial 12S rRNA and tRNA super(S) super(e) super(r) super(() super(U) super(C) super(N) super()) genes in Tunisian patients with nonsyndromic hearing loss

Molecular prenatal diagnosis of muscular dystrophies in Tunisia and postnatal follow-up role

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients

Are Islamic finance innovations enough for investors to escape from a financial downturn? Further evidence from portfolio simulations

Devenir des étudiants de troisième cycle de médecine générale de Saint-Étienne entre 2014 et 2020

Cu0-loaded SBA-15@ZnO with improved electrical properties and affinity towards hydrogen

Metal-organo-zinc oxide materials: Investigation on the structural, optical and electrical properties

CAD/CAE integration: updating the CAD model after a FEM analysis

A methodology for enhanced flexibility of integrated assessment in agriculture

Retrieve reusable 3D CAD objects based on hidden Markov models (HMM)

Electrochemical oxidation of succinic acid in aqueous solutions using boron doped diamond anodes

Cu 0 -loaded SBA-15@ZnO with improved electrical properties and affinity towards hydrogen

Electrochemical degradation of an anionic surfactant on boron-doped diamond anodes

Electrochemical Oxidation of Benzoic Acid Derivatives on Boron Doped Diamond: Voltammetric Study and Galvanostatic Electrolyses

Proposition of a Geometric Complexity Model for Additive Manufacturing Process Based on CAD

Generic Bio-Economic Farm Model for Environmental and Economic Assessment of Agricultural Systems

Suchergebnisse filtern