UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 211

Sortiert nach

160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker–Warburg syndrome

European journal of medical genetics, 2013-12, Vol.56 (12), p.689-694

2013

Volltextzugriff (PDF)

45,X/46,X,dic(Y)-Mosaicism in the Newborn

Klinische Pädiatrie, 2005-09, Vol.217 (5), p.300-303

2005

Volltextzugriff (PDF)

AA-type amyloidosis associated with non-Hodgkin’s lymphoma: A case report

Human pathology, 2004-08, Vol.35 (8), p.1041-1044

2004

Volltextzugriff (PDF)

Access to and safety of COVID-19 convalescent plasma in the United States Expanded Access Program: A national registry study

PLoS medicine, 2021-12, Vol.18 (12), p.e1003872-e1003872

2021

Volltextzugriff (PDF)

Alterations of the retinoblastoma gene in clinically localized, stage B prostate adenocarcinomas

Human pathology, 1996, Vol.27 (1), p.28-34

1996

Volltextzugriff (PDF)

Analysis of independent microarray datasets of renal biopsies identifies a robust transcript signature of acute allograft rejection

Transplant international, 2009-03, Vol.22 (3), p.293-302

2009

Volltextzugriff (PDF)

Analysis of static balance performance and dynamic postural priority according to playing position in elite soccer players

Gait & posture, 2019-10, Vol.74, p.148-153

2019

Volltextzugriff (PDF)

Approach to acute renal failure in biopsy proven myeloma cast nephropathy: Is there still a role for plasmapheresis?

Kidney international, 2008-10, Vol.74 (7), p.956-961

2008

Volltextzugriff (PDF)

Are There Differences in Concentric Isokinetic Strength Perfor-Mance Profiles between International and Non-International Elite Soccer Players?

International journal of environmental research and public health, 2020-12, Vol.18 (1), p.35

2020

Volltextzugriff (PDF)

Areas of slow conduction in atrial re-entrant tachycardia: a case report and review of the literature

International journal of cardiology, 1993-09, Vol.41 (2), p.133-139

1993

Volltextzugriff (PDF)

Assessing clinical generalizability in sedation studies of upper GI endoscopy

Gastrointestinal endoscopy, 2004-07, Vol.60 (1), p.28-33

2004

Volltextzugriff (PDF)

Association between endothelial progenitor cell depletion in blood and mild-to-moderate renal insufficiency in stable angina

Nephrology, dialysis, transplantation, 2008-07, Vol.23 (7), p.2265-2273

2008

Volltextzugriff (PDF)

Association Between Multimorbidity and Rate of Falls: A 3-Year 5-Country Prospective Study in Generally Healthy and Active Community-Dwelling Adults Aged ≥70 Years

Journal of the American Medical Directors Association, 2023-06, Vol.24 (6), p.804-810.e4

2023

Volltextzugriff (PDF)

Association between plasma selenium level and NRF2 target genes expression in humans

Journal of trace elements in medicine and biology, 2015-04, Vol.30, p.102-106

2015

Volltextzugriff (PDF)

Association Between Visual Acuity and Prospective Fall Risk in Generally Healthy and Active Older Adults: The 3-Year DO-HEALTH Study

Journal of the American Medical Directors Association, 2024-05, Vol.25 (5), p.789-795.e2

2024

Volltextzugriff (PDF)

Association of a TNFSF13B (BAFF) regulatory region single nucleotide polymorphism with response to rituximab in antineutrophil cytoplasmic antibody–associated vasculitis

Journal of allergy and clinical immunology, 2017-05, Vol.139 (5), p.1684-1687.e10

2017

Volltextzugriff (PDF)

Asymmetric dimethylarginine reflects cumulative inflammatory burden in rheumatoid arthritis. A novel mechanism of excessive cardiovascular morbidity?

Rheumatology (Oxford, England), 2015-07, Vol.54 (7), p.1135-1136

2015

Volltextzugriff (PDF)

Avoidance of Smoky Establishments: Findings From Erie and Niagara Counties in New York

Journal of public health management and practice, 2004-11, Vol.10 (6), p.508-510

2004

Volltextzugriff (PDF)

Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

European journal of human genetics : EJHG, 2017-02, Vol.25 (2), p.183-191

2017

Volltextzugriff (PDF)

BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients

Blood cells, molecules, & diseases, 2013-01, Vol.50 (1), p.33-38

2013

Volltextzugriff (PDF)

Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly

American journal of human genetics, 2019-10, Vol.105 (4), p.869-878

2019

Volltextzugriff (PDF)

Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities

American journal of human genetics, 2020-02, Vol.106 (2), p.246-255

2020

Volltextzugriff (PDF)

Biodegradable Polymer Versus Permanent Polymer Drug-Eluting Stents and Everolimus- Versus Sirolimus-Eluting Stents in Patients With Coronary Artery Disease: 3-Year Outcomes From a Randomized Clinical Trial

Journal of the American College of Cardiology, 2011-09, Vol.58 (13), p.1325-1331

2011

Volltextzugriff (PDF)

Biological variation for N-Terminal Pro- and B-type natriuretic peptides and implications for therapeutic monitoring of patients with congestive heart failure

The American journal of cardiology, 2003-09, Vol.92 (5), p.628-631

2003

Volltextzugriff (PDF)

1 – 25 von 211

Suche als RSS-Feed

Aktive Filter

KollektionSpringer Nature - Complete Springer Journals

Zeitschrift / SerieJournal Of Geophysical Research. Planets

Zeitschrift / SerieMolecules

Zeitschrift / SerieScientific Reports

SpracheItalienisch

PublikationsformReferenzeintrag

ThemaAnimals

ThemaChemistry, Physical

ThemaTechnology

KollektionIngenta

Nur zeigenMit Volltextzugriff

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(211)

Publikationsform

Artikel
(211)

Sprache

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker–Warburg syndrome

45,X/46,X,dic(Y)-Mosaicism in the Newborn

AA-type amyloidosis associated with non-Hodgkin’s lymphoma: A case report

Access to and safety of COVID-19 convalescent plasma in the United States Expanded Access Program: A national registry study

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Alterations of the retinoblastoma gene in clinically localized, stage B prostate adenocarcinomas

Analysis of independent microarray datasets of renal biopsies identifies a robust transcript signature of acute allograft rejection

Analysis of static balance performance and dynamic postural priority according to playing position in elite soccer players

Approach to acute renal failure in biopsy proven myeloma cast nephropathy: Is there still a role for plasmapheresis?

Are There Differences in Concentric Isokinetic Strength Perfor-Mance Profiles between International and Non-International Elite Soccer Players?

Areas of slow conduction in atrial re-entrant tachycardia: a case report and review of the literature

Assessing clinical generalizability in sedation studies of upper GI endoscopy

Association between endothelial progenitor cell depletion in blood and mild-to-moderate renal insufficiency in stable angina

Association Between Multimorbidity and Rate of Falls: A 3-Year 5-Country Prospective Study in Generally Healthy and Active Community-Dwelling Adults Aged ≥70 Years

Association between plasma selenium level and NRF2 target genes expression in humans

Association Between Visual Acuity and Prospective Fall Risk in Generally Healthy and Active Older Adults: The 3-Year DO-HEALTH Study

Association of a TNFSF13B (BAFF) regulatory region single nucleotide polymorphism with response to rituximab in antineutrophil cytoplasmic antibody–associated vasculitis

Asymmetric dimethylarginine reflects cumulative inflammatory burden in rheumatoid arthritis. A novel mechanism of excessive cardiovascular morbidity?

Avoidance of Smoky Establishments: Findings From Erie and Niagara Counties in New York

Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

BCL11B, FLT3, NOTCH1 and FBXW7 mutation status in T-cell acute lymphoblastic leukemia patients

Bi-allelic Variants in METTL5 Cause Autosomal-Recessive Intellectual Disability and Microcephaly

Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities

Biodegradable Polymer Versus Permanent Polymer Drug-Eluting Stents and Everolimus- Versus Sirolimus-Eluting Stents in Patients With Coronary Artery Disease: 3-Year Outcomes From a Randomized Clinical Trial

Biological variation for N-Terminal Pro- and B-type natriuretic peptides and implications for therapeutic monitoring of patients with congestive heart failure

Aktive Filter

Suchergebnisse filtern