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...

Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation

Archives of disease in childhood, 2009-01, Vol.94 (1), p.55-58

2009

Volltextzugriff (PDF)

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy

European journal of pediatrics, 1997-07, Vol.156 (7), p.562-564

1997

Volltextzugriff (PDF)

Raised serum amylase in patients with COVID-19 may not be associated with pancreatitis

British journal of surgery, 2021-04, Vol.108 (4), p.e152-e153

2021

Volltextzugriff (PDF)

Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency

Molecular genetics and metabolism, 2009, Vol.96 (1), p.38-43

2009

Volltextzugriff (PDF)

Localized cluster of nodules in childhood

Clinical and experimental dermatology, 2018-01, Vol.43 (1), p.88-90

2018

Volltextzugriff (PDF)

Chronic inflammatory acantholytic dermatosis: a previously under‐recognized or emerging variant of Grover disease

Clinical and experimental dermatology, 2017-08, Vol.42 (6), p.683-685

2017

Volltextzugriff (PDF)

Economic evaluation of a randomized clinical trial of haemodilution with cell salvage in aortic surgery

British journal of surgery, 2002-06, Vol.89 (6), p.731-736

2002

Volltextzugriff (PDF)

Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

Human molecular genetics, 1995-01, Vol.4 (1), p.1-8

1995

Volltextzugriff (PDF)

Mitochondrial DNA polymerase mutations: an ever expanding molecular and clinical spectrum

Journal of medical genetics, 2011-10, Vol.48 (10), p.669-681

2011

Volltextzugriff (PDF)

Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease

European journal of pediatrics, 1998-08, Vol.157 (8), p.643-647

1998

Volltextzugriff (PDF)

CAG repeat size and clinical presentation in Huntington's disease

Neurology, 1994-06, Vol.44 (6), p.1137-1137

1994

Volltextzugriff (PDF)

MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation

Journal of medical genetics, 2004-02, Vol.41 (2), p.125-129

2004

Volltextzugriff (PDF)

A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency

Journal of medical genetics, 2006-09, Vol.43 (9), p.e46-e46

2006

Volltextzugriff (PDF)

Discordant PKU phenotype in one family due to disparate genotypes and a novel mutation

Journal of inherited metabolic disease, 2004-01, Vol.27 (2), p.157-163

2004

Volltextzugriff (PDF)

Patterns of Genetic Variation in the Hypertension Candidate Gene GRK4: Ethnic Variation and Haplotype Structure

Annals of human genetics, 2006-01, Vol.70 (1), p.27-41

2006

Volltextzugriff (PDF)

Mitochondrial DNA mutations in a patient with sex reversal and clinical features consistent with Fraser syndrome

Clinical genetics, 2005-03, Vol.67 (3), p.252-257

2005

Volltextzugriff (PDF)

Getting It Right First Time: the national survey of surgical site infection rates in NHS trusts in England

Annals of the Royal College of Surgeons of England, 2019-09, Vol.101 (7), p.463-471

2019

Volltextzugriff (PDF)

Re: “Modification of protocol with one extra drop of endovascular cyanoacrylate improved closure rates in incompetent great saphenous veins”—time to rethink the instructions for use for VenaSeal™?

Phlebology, 2022-09, Vol.37 (8), p.616-617

2022

Volltextzugriff (PDF)

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders

Genetics in medicine, 2013-05, Vol.15 (5), p.388-394

2013

Volltextzugriff (PDF)

Re: “Do we need another modality for truncal vein ablation?” – What about microwave as an endothermal device?

Phlebology, 2021-06, Vol.36 (5), p.414-415

2021

Volltextzugriff (PDF)

Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects

Human mutation, 2013-06, Vol.34 (6), p.882-893

2013

Volltextzugriff (PDF)

Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene

Human genetics, 1998-08, Vol.103 (2), p.199-203

1998

Volltextzugriff (PDF)

A novel mutation in the mitochondrial tRNASer(AGY) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency

Journal of medical genetics, 2006-09, Vol.43 (9), p.e46-e46

2006

Volltextzugriff (PDF)

Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer

Cancer research (Chicago, Ill.), 2002-02, Vol.62 (4), p.972-976

2002

Volltextzugriff (PDF)

Biochemical characterization of pectate lyases produced by fluorescent pseudomonads associated with spoilage of fresh fruits and vegetables

Journal of applied microbiology, 1997-07, Vol.83 (1), p.10-16

1997

Volltextzugriff (PDF)

1 – 25 von 12.842

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(11.342)
Mit Volltextzugriff
(10.849)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

5 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(8.633)
Life Sciences & Biomedicine
(6.390)
Humans
(5.229)
Female
(3.216)
Male
(3.101)
Biological And Medical Sciences
(2.631)
Medical Sciences
(2.100)
Middle Aged
(2.006)
Adult
(1.872)
Physical Sciences
(1.522)
Animals
(1.514)
Aged
(1.500)
Technology
(1.121)
Physics
(881)
Adolescent
(759)
Oncology
(730)
Risk Factors
(700)
Fundamental And Applied Biological Sciences. Psychology
(675)
Exact Sciences And Technology
(631)
Mice
(610)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(6.405)
Free E-Journal (出版社公開部分のみ）
(5.831)
IngentaConnect Journals
(5.006)
Journals@Ovid Complete
(4.545)
NUS Single-Journal Subscriptions
(2.984)
Elsevier ScienceDirect Journals Complete
(2.630)
Wiley Online Library - AutoHoldings Journals
(1.763)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(1.761)
IngentaConnect Journals
(1.493)
Wiley Online Library Full Collection 2018
(1.183)
Springer Nature - Complete Springer Journals
(873)
Oxford University Press Journals Current
(730)
Nature Research
(682)
IEEE Xplore
(524)
Oxford Journals 2020 Medicine
(519)
Jstor Complete Legacy
(505)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(502)
Nexis Uni
(427)
BMJ
(279)
Taylor & Francis Journals
(241)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy

Raised serum amylase in patients with COVID-19 may not be associated with pancreatitis

Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiency

Localized cluster of nodules in childhood

Chronic inflammatory acantholytic dermatosis: a previously under‐recognized or emerging variant of Grover disease

Economic evaluation of a randomized clinical trial of haemodilution with cell salvage in aortic surgery

Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

Mitochondrial DNA polymerase mutations: an ever expanding molecular and clinical spectrum

Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison disease

CAG repeat size and clinical presentation in Huntington's disease

MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation

A novel mutation in the mitochondrial tRNA(Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency

Discordant PKU phenotype in one family due to disparate genotypes and a novel mutation

Patterns of Genetic Variation in the Hypertension Candidate Gene GRK4: Ethnic Variation and Haplotype Structure

Mitochondrial DNA mutations in a patient with sex reversal and clinical features consistent with Fraser syndrome

Getting It Right First Time: the national survey of surgical site infection rates in NHS trusts in England

Re: “Modification of protocol with one extra drop of endovascular cyanoacrylate improved closure rates in incompetent great saphenous veins”—time to rethink the instructions for use for VenaSeal™?

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders

Re: “Do we need another modality for truncal vein ablation?” – What about microwave as an endothermal device?

Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects

Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene

A novel mutation in the mitochondrial tRNASer(AGY) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency

Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer

Biochemical characterization of pectate lyases produced by fluorescent pseudomonads associated with spoilage of fresh fruits and vegetables

Suchergebnisse filtern