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...

Clinical characteristics of and growth hormone treatment effects on short stature with type 1 insulin-like growth factor receptor (IGF1R) gene alteration

Endocrine Journal, 2024, Vol.71(7), pp.687-694

2024

Volltextzugriff (PDF)

Independent predictors of discordance between the resting full-cycle ratio and fractional flow reserve

Heart and vessels, 2021-06, Vol.36 (6), p.790-798

2021

Volltextzugriff (PDF)

Genetic causes of growth hormone insensitivity beyond GHR

Reviews in endocrine & metabolic disorders, 2021-03, Vol.22 (1), p.43-58

2021

Volltextzugriff (PDF)

Clinical feasibility of resting full-cycle ratio as a unique non-hyperemic index of invasive functional lesion assessment

Heart and vessels, 2020-11, Vol.35 (11), p.1518-1526

2020

Volltextzugriff (PDF)

Diagnostic Performance of High-Resolution Intravascular Ultrasound for the Detection of Plaque Rupture in Patients With Acute Coronary Syndrome

Circulation Journal, 2019/11/25, Vol.83(12), pp.2505-2511

2019

Volltextzugriff (PDF)

Novel Modulators of the Growth Hormone - Insulin-Like Growth Factor Axis: Pregnancy-Associated Plasma Protein-A2 and Stanniocalcin-2

Journal of clinical research in pediatric endocrinology, 2017-12, Vol.9 (Suppl 2), p.1-8

2017

Volltextzugriff (PDF)

Utility of new FDG-PET/CT guidelines for diagnosing cardiac sarcoidosis in patients with implanted cardiac pacemakers for atrioventricular block

Scientific reports, 2024-04, Vol.14 (1), p.7825-7825, Article 7825

2024

Volltextzugriff (PDF)

Surgical revascularization for severe spasm in the left main coronary artery

Clinical case reports, 2023-01, Vol.11 (1), p.e6815-n/a

2023

Volltextzugriff (PDF)

Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation

Endocrinology (Philadelphia), 2019-06, Vol.160 (6), p.1363-1376

2019

Volltextzugriff (PDF)

Alström Syndrome: A Review Focusing on Its Diverse Clinical Manifestations and Their Etiology as a Ciliopathy

Yonago Acta Medica, 2024-05, Vol.67 (2), p.93-99, Article 2024.05.010

2024

Volltextzugriff (PDF)

Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1

Hormone research in paediatrics, 2018-01, Vol.89 (3), p.205-210

2018

Volltextzugriff (PDF)

Switching to burosumab from conventional therapy in siblings with relatively well-controlled X-linked hypophosphatemia

Clinical Pediatric Endocrinology, 2024, Vol.33(1), pp.27-34

2024

Volltextzugriff (PDF)

Cord Blood from SGA Preterm Infants Exhibits Increased GLUT4 mRNA Expression

YONAGO ACTA MEDICA, 2021, Vol.64 (1), p.57-66

2021

Volltextzugriff (PDF)

Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations

Clinical Pediatric Endocrinology, 2022, Vol.31(2), pp.59-67

2022

Volltextzugriff (PDF)

Tissue characteristics of residual lesion in patients with acute coronary syndrome caused by plaque rupture versus plaque erosion: a single-center, retrospective, observational study

Nagoya journal of medical science, 2024-05, Vol.86 (2), p.189-200

2024

Volltextzugriff (PDF)

Association between coronary flow and aortic stenosis during transcatheter aortic valve implantation

ESC Heart Failure, 2023-06, Vol.10 (3), p.2031-2041

2023

Volltextzugriff (PDF)

A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor: a family with renal pseudohypoaldosteronism type 1

Endocrine Journal, 2017, Vol.64(1), pp.83-90

2017

Volltextzugriff (PDF)

Feasibility and safety of intracoronary nicorandil infusion as a novel hyperemic agent for fractional flow reserve measurements

Heart and vessels, 2015-07, Vol.30 (4), p.477-483

2015

Volltextzugriff (PDF)

Leprechaunism (Donohue syndrome): A case bearing novel compound heterozygous mutations in the insulin receptor gene

Endocrine Journal, 2013, Vol.60(1), pp.107-112

2013

Volltextzugriff (PDF)

Impact of skeletal muscle mass on clinical outcomes in patients with severe aortic stenosis undergoing transcatheter aortic valve replacement

Cardiovascular intervention and therapeutics, 2021-10, Vol.36 (4), p.514-522

2021

Volltextzugriff (PDF)

Disorders caused by genetic defects associated with GH-dependent genes: PAPPA2 defects

Molecular and cellular endocrinology, 2020-12, Vol.518, p.110967-110967, Article 110967

2020

Volltextzugriff (PDF)

A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia

Endocrine Journal, 2015, Vol.62(1), pp.101-106

2015

Volltextzugriff (PDF)

Clinical Overview of Nephrogenic Diabetes Insipidus Based on a Nationwide Survey in Japan

YONAGO ACTA MEDICA, 2014-06, Vol.57 (2), p.85-91

2014

Volltextzugriff (PDF)

A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor : a family with renal pseudohypoaldosteronism type 1

ENDOCRINE JOURNAL, 2017-01, Vol.64 (1), p.83-90

2017

Volltextzugriff (PDF)

Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord Blood

Journal of the Endocrine Society, 2017-12, Vol.1 (12), p.1408-1416

2017

Volltextzugriff (PDF)

1 – 25 von 267

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(187)
Mit Volltextzugriff
(224)

Publikationsform

Sprache

Englisch
(215)
Japanisch
(62)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(4)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Clinical characteristics of and growth hormone treatment effects on short stature with type 1 insulin-like growth factor receptor (IGF1R) gene alteration

Independent predictors of discordance between the resting full-cycle ratio and fractional flow reserve

Genetic causes of growth hormone insensitivity beyond GHR

Clinical feasibility of resting full-cycle ratio as a unique non-hyperemic index of invasive functional lesion assessment

Diagnostic Performance of High-Resolution Intravascular Ultrasound for the Detection of Plaque Rupture in Patients With Acute Coronary Syndrome

Novel Modulators of the Growth Hormone - Insulin-Like Growth Factor Axis: Pregnancy-Associated Plasma Protein-A2 and Stanniocalcin-2

Utility of new FDG-PET/CT guidelines for diagnosing cardiac sarcoidosis in patients with implanted cardiac pacemakers for atrioventricular block

Surgical revascularization for severe spasm in the left main coronary artery

Low IGF-I Bioavailability Impairs Growth and Glucose Metabolism in a Mouse Model of Human PAPPA2 p.Ala1033Val Mutation

Alström Syndrome: A Review Focusing on Its Diverse Clinical Manifestations and Their Etiology as a Ciliopathy

Adrenal Insufficiency, Sex Reversal, and Angelman Syndrome due to Uniparental Disomy Unmasking a Mutation in CYP11A1

Switching to burosumab from conventional therapy in siblings with relatively well-controlled X-linked hypophosphatemia

Cord Blood from SGA Preterm Infants Exhibits Increased GLUT4 mRNA Expression

Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations

Tissue characteristics of residual lesion in patients with acute coronary syndrome caused by plaque rupture versus plaque erosion: a single-center, retrospective, observational study

Association between coronary flow and aortic stenosis during transcatheter aortic valve implantation

A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor: a family with renal pseudohypoaldosteronism type 1

Feasibility and safety of intracoronary nicorandil infusion as a novel hyperemic agent for fractional flow reserve measurements

Leprechaunism (Donohue syndrome): A case bearing novel compound heterozygous mutations in the insulin receptor gene

Impact of skeletal muscle mass on clinical outcomes in patients with severe aortic stenosis undergoing transcatheter aortic valve replacement

Disorders caused by genetic defects associated with GH-dependent genes: PAPPA2 defects

A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia

Clinical Overview of Nephrogenic Diabetes Insipidus Based on a Nationwide Survey in Japan

A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor : a family with renal pseudohypoaldosteronism type 1

Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord Blood

Suchergebnisse filtern