1
Sertraline for the Treatment of Major Depressive Disorder in the US: Effectiveness and Acceptability in Real-World Practice

von Correll CU ; Purushottamahanti P ; Subramaniam K ; et al.

Neuropsychiatric Disease and Treatment, Vol 22, Iss Issue 1, Pp 1-14 (2026)

Schlagworte: Antidepressants; Clinical Global Impression – Severity; Major depressive disorder; Real-world evidence; Sertraline; United States; Neurosciences. Biological psychiatry. Neuropsychiatry; RC321-571; Neurology. Diseases of the nervous system; RC346-429
- Zum Volltext in DOAJ
Merkliste

2
New Strategies to Improve Patient Adherence to Medications for Noncommunicable Diseases During and After the COVID-19 Era Identified via a Literature Review

von Hassan TA ; Sáenz JE ; Ducinskiene D ; et al.

Journal of Multidisciplinary Healthcare, Vol 14, Pp 2453-2465 (2021)

Schlagworte: patients; adherence; persistence; noncommunicable diseases; covid-19; telemedicine; ehealth; Medicine (General); R5-920
- Zum Volltext in DOAJ
Merkliste

3
A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts

von Bravo, Laura ; Simões, Joana FF ; Cardoso, Victor R ; et al.

In The Lancet Digital Health July 2024 6(7):e507-e519
- View full text via DOI
Merkliste

4
Life expectancy associated with different ages at diagnosis of type 2 diabetes in high-income countries: 23 million person-years of observation

von Kaptoge, S ; Seshasai, SRK ; Sun, L ; et al.

In The Lancet Diabetes & Endocrinology October 2023 11(10):731-742
- View full text via DOI
Merkliste

5
Evaluation of prognostic risk models for postoperative pulmonary complications in adult patients undergoing major abdominal surgery: a systematic review and international external validation cohort study

von Kouli, O ; Murray, V ; Bhatia, S ; et al.

In The Lancet Digital Health July 2022 4(7):e520-e531
- View full text via DOI
Merkliste

6
Mesonephric‐type adenocarcinomas of the ovary: prevalence, diagnostic reproducibility, outcome, and value of PAX2

von Martin Köbel ; Eun Young Kang ; Sandra Lee ; et al.

The Journal of Pathology: Clinical Research, Vol 10, Iss 4, Pp n/a-n/a (2024)

Schlagworte: mesonephric; mesonephric‐like; PAX2; GATA3; TTF1; Pathology; RB1-214
- View full text via DOI
Merkliste

7
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy

von Zheng, SL ; Henry, A ; Cannie, D ; et al.
- View full text via BASE
Merkliste

8
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

von Keaton JM ; Kamali Z ; Xie T ; et al.

Nature Genetics, 1 May 2024
- View full text via BASE
Merkliste

9
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

von Keaton, JM ; Kamali, Z ; Xie, T ; et al.
- View full text via BASE
Merkliste

10
Higher burden of cardiometabolic and socioeconomic risk factors in women with type 2 diabetes: an analysis of the Glycemic Reduction Approaches in Diabetes (GRADE) baseline cohort

von C Wright ; C Sanders ; C Wilson ; et al.

BMJ Open Diabetes Research & Care, Vol 11, Iss 2 (2023)

Schlagworte: Diseases of the endocrine glands. Clinical endocrinology; RC648-665
- View full text via DOI
Merkliste

11
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

von Young, WJ ; Lahrouchi, N ; Isaacs, A ; et al.

Schlagworte: Genome-wide association studies; Genetic markers
- View full text via BASE
Merkliste

12
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.

von Shrine, N ; Izquierdo, AG ; Chen, J ; et al.
- View full text via BASE
Merkliste

13
Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.

von Shrine, N ; Izquierdo, AG ; Chen, J ; et al.
- View full text via BASE
Merkliste

14
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

von Gorski, M ; Rasheed, H ; Teumer, A ; et al.

urn:ISSN:0085-2538 ; urn:ISSN:1523-1755 ; Kidney International, 102, 3, 624-639

Schlagworte: 32 Biomedical and Clinical Sciences; 3202 Clinical Sciences; Human Genome; Kidney Disease; Clinical Research; Prevention; Genetics; 2.1 Biological and endogenous factors; Renal and urogenital; Cross-Sectional Studies; Genetic Loci; Genome-Wide Association Study; Glomerular Filtration Rate; Humans; Kidney; Longitudinal Studies; N-Acetylgalactosaminyltransferases; Renal Insufficiency; Chronic; acute kidney injury; chronic kidney disease; diabetes; gene expression; Lifelines Cohort Study; anzsrc-for: 32 Biomedical and Clinical Sciences; anzsrc-for: 3202 Clinical Sciences; anzsrc-for: 1103 Clinical Sciences
- View full text via BASE
Merkliste

15
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes

von Pervjakova, N ; Moen, G-H ; Borges, M-C ; et al.
- View full text via BASE
Merkliste

16
Inactivated varicella zoster vaccine in autologous haemopoietic stem-cell transplant recipients: an international, multicentre, randomised, double-blind, placebo-controlled trial

von Basso, AC ; Bonvehi, P ; Cerana, S ; et al.

In The Lancet 26 May-1 June 2018 391(10135):2116-2127
- View full text via DOI
Merkliste

17
Shape of the OGTT glucose response curve: relationship with β-cell function and differences by sex, race, and BMI in adults with early type 2 diabetes treated with metformin

von C Wright ; C Wilson ; L Tucker ; et al.

BMJ Open Diabetes Research & Care, Vol 9, Iss 1 (2021)

Schlagworte: Diseases of the endocrine glands. Clinical endocrinology; RC648-665
- View full text via DOI
Merkliste

18
The genomics of heart failure: design and rationale of the HERMES consortium

von Lumbers, RT ; Shah, S ; Lin, H ; et al.

ESC Heart Failure (2021) (In press).

Schlagworte: Heart failure; Cardiomyopathy; Genetics; Biomarkers; Association studies
- View full text via BASE
Merkliste

19
Developing a model for effective leadership in healthcare: a concept mapping approach

von Hargett CW ; Doty JP ; Hauck JN ; et al.

Journal of Healthcare Leadership, Vol 9, Pp 69-78 (2017)

Schlagworte: Core competencies; Healthcare leadership; Medical education; Mental models; Mixed methods research; Public aspects of medicine; RA1-1270
- Zum Volltext in DOAJ
Merkliste

20
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.

von Teumer, A ; Li, Y ; Ghasemi, S ; et al.
- View full text via BASE
Merkliste

21
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

von Henry, A ; Roselli, C ; Lin, H ; et al.
- View full text via BASE
Merkliste

22
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

von Ntalla, I ; Weng, L-C ; Cartwright, JH ; et al.

Nature Communications , 11 (1) , Article 2542. (2020)

Schlagworte: Cardiovascular diseases; Cardiovascular genetics; Genome-wide association studies
- View full text via BASE
Merkliste

23
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

von Shah, S ; Henry, A ; Roselli, C ; et al.

Nature Communications , 11 , Article 163. (2020)

Schlagworte: Cardiovascular genetics; Epidemiology; Genome-wide association studies; Heart failure
- View full text via BASE
Merkliste

24
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

von Moll, M ; Sakornsakolpat, P ; Shrine, N ; et al.
- View full text via BASE
Merkliste

25
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.

von Gallagher, CS ; Mäkinen, N ; Harris, HR ; et al.

Schlagworte: Adult; Ataxia Telangiectasia Mutated Proteins; Endometriosis; Female; Forkhead Box Protein O1; Genome-Wide Association Study; Humans; Leiomyoma; Mendelian Randomization Analysis; Menorrhagia; Middle Aged; Polymorphism; Single Nucleotide; Proportional Hazards Models; Receptor; Fibroblast Growth Factor; Type 4; Signal Transduction; Telomerase; Uterine Neoplasms; White People
- View full text via BASE
Merkliste

12 3 4 5 6 7 8 9 10 11 weiter »

Sie haben nicht gefunden, wonach Sie gesucht haben? Diese Services können Ihnen weiterhelfen.
Hilfe & Kontakt ǀ Fernleihe | Hilfe zur Fernleihe ǀ Literaturvorschlag| Literaturvorschlag