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...

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

Genetics in medicine, 2009-01, Vol.11 (1), p.42-65

2009

Volltextzugriff (PDF)

Diagnosis, testing, treatment, and outcomes among patients with advanced non‐small cell lung cancer in the United States

Cancer medicine (Malden, MA), 2023-12, Vol.12 (24), p.21605-21614

2023

Volltextzugriff (PDF)

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-11, Vol.23 (11), p.2029-2037

2021

Volltextzugriff (PDF)

A Rapid-ACCE review of CYP2C9 and VKORC1 alleles testing to inform warfarin dosing in adults at elevated risk for thrombotic events to avoid serious bleeding

Genetics in medicine, 2008-02, Vol.10 (2), p.89-98

2008

Volltextzugriff (PDF)

Variability in Thyroid-Stimulating Hormone Suppression by Human Chronic Gonadotropin during Early Pregnancy

The journal of clinical endocrinology and metabolism, 2008-09, Vol.93 (9), p.3341-3347

2008

Volltextzugriff (PDF)

Gaucher disease type 1 patients from the ICGG Gaucher Registry sustain initial clinical improvements during twenty years of imiglucerase treatment

Molecular genetics and metabolism, 2021-02, Vol.132 (2), p.100-111

2021

Volltextzugriff (PDF)

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies

Genetics in medicine, 2022-07, Vol.24 (7), p.1379-1391

2022

Volltextzugriff (PDF)

Real‐world effectiveness of eliglustat in treatment‐naïve and switch patients enrolled in the International Collaborative Gaucher Group Gaucher Registry

American journal of hematology, 2020-09, Vol.95 (9), p.1038-1046

2020

Volltextzugriff (PDF)

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies

Genetics in medicine, 2022-09, Vol.24 (9), p.1992-1992

2022

Volltextzugriff (PDF)

Sequential first- and second-trimester TSH, free thyroxine, and thyroid antibody measurements in women with known hypothyroidism: a FaSTER trial study

American journal of obstetrics and gynecology, 2008-08, Vol.199 (2), p.129.e1-129.e6

2008

Volltextzugriff (PDF)

Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

Journal of medical genetics, 2007-10, Vol.44 (10), p.621-628

2007

Volltextzugriff (PDF)

A Survey of the Preferences of Primary Care Physicians Regarding the Comanagement With Specialists of Children With Rare or Complex Conditions

Clinical pediatrics, 2014-06, Vol.53 (6), p.566-570

2014

Volltextzugriff (PDF)

Critical Congenital Heart Disease Newborn Screening Implementation: Lessons Learned

Maternal and child health journal, 2017-06, Vol.21 (6), p.1240-1249

2017

Volltextzugriff (PDF)

Thyroperoxidase and thyroglobulin antibodies in early pregnancy and preterm delivery

Obstetrics and gynecology (New York. 1953), 2010-07, Vol.116 (1), p.58-62

2010

Volltextzugriff (PDF)

Trends in the Diabetes Quality Improvement Project Measures in Maine From 1994 to 1999

Diabetes care, 2003-03, Vol.26 (3), p.597-601

2003

Volltextzugriff (PDF)

Using State Birth Defects Registries to Evaluate Regional Critical Congenital Heart Disease Newborn Screening

Birth defects research, 2017-11, Vol.109 (18), p.1414-1422

2017

Volltextzugriff (PDF)

Urine Iodine Measurements, Creatinine Adjustment, and Thyroid Deficiency in an Adult United States Population

The journal of clinical endocrinology and metabolism, 2007-03, Vol.92 (3), p.1019-1022

2007

Volltextzugriff (PDF)

Erratum to: Critical Congenital Heart Disease Newborn Screening Implementation: Lessons Learned

Maternal and child health journal, 2017-07, Vol.21 (7), p.1590-1590

2017

Volltextzugriff (PDF)

National Survey of Providers Treating Patients With Metabolic Disorders Identified by Newborn Screening Demonstrates Challenges Faced by Clinical Care Systems

Clinical pediatrics, 2015-07, Vol.54 (8), p.759-764

2015

Volltextzugriff (PDF)

Thyroperoxidase and thyroglobulin antibodies in early pregnancy and placental abruption

Obstetrics and gynecology (New York. 1953), 2011-02, Vol.117 (2 Pt 1), p.287-292

2011

Volltextzugriff (PDF)

Adjusting the estimated proportion of breast cancer cases associated with BRCA1 and BRCA2 mutations: Public health implications

Genetics in medicine, 2005-01, Vol.7 (1), p.28-33

2005

Volltextzugriff (PDF)

Rapid ACCE: experience with a rapid and structured approach for evaluating gene-based testing

Genetics in medicine, 2007-07, Vol.9 (7), p.473-478

2007

Volltextzugriff (PDF)

Screening for thyroid disorders during pregnancy: Results of a survey in Maine

American journal of obstetrics and gynecology, 2006-02, Vol.194 (2), p.471-474

2006

Volltextzugriff (PDF)

How reliable are BRCA1/2 mutation estimates?

Cancer research (Chicago, Ill.), 2007-05, Vol.67 (10), p.5057; author reply 5057-5057

2007

Volltextzugriff (PDF)

Screen-positive rates and agreement among six family history screening protocols for breast/ovarian cancer in a population-based cohort of 21- to 55-year-old women

Genetics in medicine, 2006-03, Vol.8 (3), p.161-168

2006

Volltextzugriff (PDF)

1 – 25 von 46

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(45)
Bücher
(1)

Sprache

Englisch
(46)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

Diagnosis, testing, treatment, and outcomes among patients with advanced non‐small cell lung cancer in the United States

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

A Rapid-ACCE review of CYP2C9 and VKORC1 alleles testing to inform warfarin dosing in adults at elevated risk for thrombotic events to avoid serious bleeding

Variability in Thyroid-Stimulating Hormone Suppression by Human Chronic Gonadotropin during Early Pregnancy

Gaucher disease type 1 patients from the ICGG Gaucher Registry sustain initial clinical improvements during twenty years of imiglucerase treatment

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies

Real‐world effectiveness of eliglustat in treatment‐naïve and switch patients enrolled in the International Collaborative Gaucher Group Gaucher Registry

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies

Sequential first- and second-trimester TSH, free thyroxine, and thyroid antibody measurements in women with known hypothyroidism: a FaSTER trial study

Mutation detection in the ABCC6 gene and genotype–phenotype analysis in a large international case series affected by pseudoxanthoma elasticum

A Survey of the Preferences of Primary Care Physicians Regarding the Comanagement With Specialists of Children With Rare or Complex Conditions

Critical Congenital Heart Disease Newborn Screening Implementation: Lessons Learned

Thyroperoxidase and thyroglobulin antibodies in early pregnancy and preterm delivery

Trends in the Diabetes Quality Improvement Project Measures in Maine From 1994 to 1999

Using State Birth Defects Registries to Evaluate Regional Critical Congenital Heart Disease Newborn Screening

Urine Iodine Measurements, Creatinine Adjustment, and Thyroid Deficiency in an Adult United States Population

Erratum to: Critical Congenital Heart Disease Newborn Screening Implementation: Lessons Learned

National Survey of Providers Treating Patients With Metabolic Disorders Identified by Newborn Screening Demonstrates Challenges Faced by Clinical Care Systems

Thyroperoxidase and thyroglobulin antibodies in early pregnancy and placental abruption

Adjusting the estimated proportion of breast cancer cases associated with BRCA1 and BRCA2 mutations: Public health implications

Rapid ACCE: experience with a rapid and structured approach for evaluating gene-based testing

Screening for thyroid disorders during pregnancy: Results of a survey in Maine

How reliable are BRCA1/2 mutation estimates?

Screen-positive rates and agreement among six family history screening protocols for breast/ovarian cancer in a population-based cohort of 21- to 55-year-old women

Suchergebnisse filtern