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...

In the Treatment of Lateral Epicondylitis by Percutaneous Perforation, Injectables Have No Added Value

Clinical orthopaedics and related research, 2024-02, Vol.482 (2), p.325-336

2024

Volltextzugriff (PDF)

Effectiveness of standardized ultrasound guided percutaneous treatment of lateral epicondylitis with application of autologous blood, dextrose or perforation only on pain: a study protocol for a multi-center, blinded, randomized controlled trial with a 1 year follow up

BMC musculoskeletal disorders, 2019-07, Vol.20 (1), p.351-351, Article 351

2019

Volltextzugriff (PDF)

Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol

Journal of neuro-oncology, 2023-03, Vol.162 (1), p.225-235

2023

Volltextzugriff (PDF)

Bleeding complications of thromboprophylaxis with dabigatran, nadroparin or rivaroxaban for 6 weeks after total knee arthroplasty surgery: a randomised pilot study

BMJ open, 2021-01, Vol.11 (1), p.e040336

2021

Volltextzugriff (PDF)

Snapping of the annular ligament: a uncommon injury characterised by snapping or locking of the elbow with good surgical outcomes

Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA, 2019-01, Vol.27 (1), p.326-333

2019

Volltextzugriff (PDF)

Direct treatment comparison of DAbigatran and RIvaroxaban versus NAdroparin in the prevention of venous thromboembolism after total knee arthroplasty surgery: design of a randomised pilot study (DARINA)

BMJ open, 2013-01, Vol.3 (1), p.e002218

2013

Volltextzugriff (PDF)

Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1

Human molecular genetics, 1996-07, Vol.5 (7), p.1035-1041

1996

Volltextzugriff (PDF)

Ambulation with the reciprocating-gait orthosis: Experience in 15 children with myelomeningocele or paraplegia

Acta orthopaedica, 1997, Vol.68 (5), p.470-473

1997

Volltextzugriff (PDF)

Partial matrix excision or segmental phenolization for ingrowing toenails

Archives of surgery (Chicago. 1960), 2002-03, Vol.137 (3), p.320

2002

Volltextzugriff (PDF)

Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population

Genomics (San Diego, Calif.), 1994-08, Vol.22 (3), p.499-504

1994

Volltextzugriff (PDF)

The Stanmore total hip replacement. A 22-year follow-up

Journal of bone and joint surgery. British volume, 2000-01, Vol.82 (1), p.97

2000

Volltextzugriff (PDF)

Oculocerebrocutaneous syndrome

Journal of medical genetics, 1990-01, Vol.27 (1), p.69-70

1990

Volltextzugriff (PDF)

Complaints after total joint arthroplasty: caused by infection or metal hypersensitivity?

Nederlands tijdschrift voor geneeskunde, 2023-03, Vol.167

2023

Volltextzugriff (PDF)

Complaints after total joint arthroplasty: caused by infection or metal hypersensitivity?

Nederlands tijdschrift voor geneeskunde, 2023-03, Vol.166

2023

Volltextzugriff (PDF)

Biochemical correlates of the differential sensitivity of subtypes of human leukemia to deoxyadenosine and deoxycoformycin

Blood, 1982-11, Vol.60 (5), p.1098-1101

1982

Volltextzugriff (PDF)

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

Nature genetics, 1992-10, Vol.2 (2), p.157-160

1992

Volltextzugriff (PDF)

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene

Journal of medical genetics, 1994-12, Vol.31 (12), p.972-975

1994

Volltextzugriff (PDF)

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

Human genetics, 1989-03, Vol.81 (4), p.315-318

1989

Volltextzugriff (PDF)

Hoop voor de kamsalamander in de Ginkel

Meetnet Amfibieën Mededelingen, 2001-01

L. Bleeker

2001

Volltextzugriff (PDF)

Mutations in the candidate gene for Norrie disease

Human molecular genetics, 1992-10, Vol.1 (7), p.461-465

1992

Volltextzugriff (PDF)

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa

Genomics (San Diego, Calif.), 1992-11, Vol.14 (3), p.811-812

1992

Volltextzugriff (PDF)

Biochemical basis for the differential effects of deoxycoformycin on human leukemias

Advances in experimental medicine and biology, 1984, Vol.165 Pt B, p.305

1984

Volltextzugriff (PDF)

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

Human genetics, 1985-01, Vol.71 (3), p.211-214

1985

Volltextzugriff (PDF)

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

Cytogenetic and genome research, 1986-01, Vol.42 (4), p.219-224

1986

Volltextzugriff (PDF)

Intravenous immunoglobulin preparations induce mild activation of neutrophils in vivo via triggering of macrophages – studies in a rat model

British journal of haematology, 2001-03, Vol.112 (4), p.1031-1040

2001

Volltextzugriff (PDF)

1 – 25 von 518

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(448)
Mit Volltextzugriff
(426)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

In the Treatment of Lateral Epicondylitis by Percutaneous Perforation, Injectables Have No Added Value

Effectiveness of standardized ultrasound guided percutaneous treatment of lateral epicondylitis with application of autologous blood, dextrose or perforation only on pain: a study protocol for a multi-center, blinded, randomized controlled trial with a 1 year follow up

Medulloblastoma in adults: evaluation of the Dutch society for neuro-oncology treatment protocol

Bleeding complications of thromboprophylaxis with dabigatran, nadroparin or rivaroxaban for 6 weeks after total knee arthroplasty surgery: a randomised pilot study

Snapping of the annular ligament: a uncommon injury characterised by snapping or locking of the elbow with good surgical outcomes

Direct treatment comparison of DAbigatran and RIvaroxaban versus NAdroparin in the prevention of venous thromboembolism after total knee arthroplasty surgery: design of a randomised pilot study (DARINA)

Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1

Ambulation with the reciprocating-gait orthosis: Experience in 15 children with myelomeningocele or paraplegia

Partial matrix excision or segmental phenolization for ingrowing toenails

Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population

The Stanmore total hip replacement. A 22-year follow-up

Oculocerebrocutaneous syndrome

Complaints after total joint arthroplasty: caused by infection or metal hypersensitivity?

Complaints after total joint arthroplasty: caused by infection or metal hypersensitivity?

Biochemical correlates of the differential sensitivity of subtypes of human leukemia to deoxyadenosine and deoxycoformycin

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp

Hoop voor de kamsalamander in de Ginkel

Mutations in the candidate gene for Norrie disease

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa

Biochemical basis for the differential effects of deoxycoformycin on human leukemias

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

Intravenous immunoglobulin preparations induce mild activation of neutrophils in vivo via triggering of macrophages – studies in a rat model

Suchergebnisse filtern