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...

Neuraxial anesthesia for delivery in parturtients with Brugada syndrome: Local anesthetics revisited

Journal of gynecology obstetrics and human reproduction, 2023-05, Vol.52 (5), p.102562-102562, Article 102562

2023

Volltextzugriff (PDF)

Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2015-10, Vol.100 (10), p.1301-1310

2015

Volltextzugriff (PDF)

The EBV-MS connection: the enigma remains

Frontiers in immunology, 2024-08, Vol.15, p.1466339

2024

Volltextzugriff (PDF)

Which immune cells matter? The immunopathogenesis of multiple sclerosis

Critical reviews in immunology, 2013, Vol.33 (4), p.283-306

2013

Volltextzugriff (PDF)

Implication of fatty acids in the inhibitory effect of human adipocytes on osteoblastic differentiation

Bone (New York, N.Y.), 2013-08, Vol.55 (2), p.429-430

2013

Volltextzugriff (PDF)

Haplotype 4 of the multiple sclerosis-associated interleukin-7 receptor alpha gene influences the frequency of recent thymic emigrants

Genes and immunity, 2010-06, Vol.11 (4), p.326-333

2010

Volltextzugriff (PDF)

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Cell, 1995-04, Vol.81 (1), p.27-40

1995

Volltextzugriff (PDF)

The influence of interleukin-7 receptor α-chain haplotypes on outcome after allogeneic hematopoietic cell transplantation

International journal of immunogenetics, 2014-12, Vol.41 (6), p.521-527

2014

Volltextzugriff (PDF)

Sutured perineal omentoplasty after abdominoperineal resection for adenocarcinoma of the lower rectum

Diseases of the colon & rectum, 2005-03, Vol.48 (3), p.476-482

2005

Volltextzugriff (PDF)

β-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

Nature genetics, 1995-11, Vol.11 (3), p.257-265

1995

Volltextzugriff (PDF)

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Annals of neurology, 1997-08, Vol.42 (2), p.222-229

1997

Volltextzugriff (PDF)

Molecular pathways supporting the proliferation staging of malignant melanoma (Review)

International journal of molecular medicine, 2009-09, Vol.24 (3), p.295-301

2009

Volltextzugriff (PDF)

Bedside adherence to clinical practice guidelines in the intensive care unit: the TECLA study

Intensive care medicine, 2008-08, Vol.34 (8), p.1393-1400

2008

Volltextzugriff (PDF)

Nursing care for Gypsies in the Saintonge country. Interview by Genevieve Binel

Soins. Pédiatrie, puériculture, 2006-06 (230), p.30

Broux, Olivier

2006

Volltextzugriff (PDF)

Molecular histology on the diagnostic cutting edge between malignant melanomas and cutaneous melanocytomas (Review)

Oncology reports, 2009-12, Vol.22 (6), p.1263-1267

2009

Volltextzugriff (PDF)

Space-time clustering and seasonality in diagnosing skin cancers in Wallonia (south-east Belgium)

Dermatology (Basel), 2008-01, Vol.217 (1), p.48-51

2008

Volltextzugriff (PDF)

Utilization of Essure® micro-insert for hydrosalpynx occlusion in infertile women

Journal de gynecologie, obstetrique et biologie de la reproduction, 2012-04, Vol.41 (2), p.145

2012

Volltextzugriff (PDF)

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval

American journal of human genetics, 1995-06, Vol.56 (6), p.1417-1430

1995

Volltextzugriff (PDF)

β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate

Neuromuscular disorders : NMD, 1998-02, Vol.8 (1), p.30-38

1998

Volltextzugriff (PDF)

Deciphering the "ugly duckling", but escaping the "telly belly". Exploratory algorithm of the diagnostic cutting edge of melanoma

Revue médicale de Liège, 2010-04, Vol.65 (4), p.180

2010

Volltextzugriff (PDF)

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy

Human molecular genetics, 1994-02, Vol.3 (2), p.285-293

1994

Volltextzugriff (PDF)

Malignant melanoma: conceptual and therapeutic innovations based on translational research

Revue médicale de Liège, 2008-10, Vol.63 (10), p.579

2008

Volltextzugriff (PDF)

Regional Localization of Human Chromosome 15 Loci

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.619-627

1994

Volltextzugriff (PDF)

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families

Journal of medical genetics, 1993-05, Vol.30 (5), p.385-387

1993

Volltextzugriff (PDF)

Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

Neuromuscular disorders : NMD, 1996-12, Vol.6 (6), p.455-462

1996

Volltextzugriff (PDF)

1 – 25 von 45

Suche als RSS-Feed

Aktive Filter

ThemaHumans

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(38)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(45)

Sprache

Englisch
(26)
Französisch
(19)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(26)
Science & Technology
(26)
Female
(20)
Adult
(13)
Male
(13)
Biological And Medical Sciences
(12)
Medical Sciences
(11)
Muscular Dystrophies - Genetics
(11)
Genetics & Heredity
(9)
Chromosomes, Human, Pair 15
(8)
Middle Aged
(8)
Adolescent
(7)
Chromosome Mapping
(7)
Base Sequence
(6)
Child
(6)
Diseases Of Striated Muscles. Neuromuscular Diseases
(6)
Neurology
(6)
Genetic Markers
(5)
Genotype
(5)

14 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Neuraxial anesthesia for delivery in parturtients with Brugada syndrome: Local anesthetics revisited

Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia

The EBV-MS connection: the enigma remains

Which immune cells matter? The immunopathogenesis of multiple sclerosis

Implication of fatty acids in the inhibitory effect of human adipocytes on osteoblastic differentiation

Haplotype 4 of the multiple sclerosis-associated interleukin-7 receptor alpha gene influences the frequency of recent thymic emigrants

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

The influence of interleukin-7 receptor α-chain haplotypes on outcome after allogeneic hematopoietic cell transplantation

Sutured perineal omentoplasty after abdominoperineal resection for adenocarcinoma of the lower rectum

β-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Molecular pathways supporting the proliferation staging of malignant melanoma (Review)

Bedside adherence to clinical practice guidelines in the intensive care unit: the TECLA study

Nursing care for Gypsies in the Saintonge country. Interview by Genevieve Binel

Molecular histology on the diagnostic cutting edge between malignant melanomas and cutaneous melanocytomas (Review)

Space-time clustering and seasonality in diagnosing skin cancers in Wallonia (south-east Belgium)

Utilization of Essure® micro-insert for hydrosalpynx occlusion in infertile women

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval

β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate

Deciphering the "ugly duckling", but escaping the "telly belly". Exploratory algorithm of the diagnostic cutting edge of melanoma

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy

Malignant melanoma: conceptual and therapeutic innovations based on translational research

Regional Localization of Human Chromosome 15 Loci

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families

Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

Aktive Filter

Suchergebnisse filtern