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...

Bartonella infection in shelter cats and dogs and their ectoparasites

Vector borne and zoonotic diseases (Larchmont, N.Y.), 2011-08, Vol.11 (8), p.1023-1030

2011

Volltextzugriff (PDF)

Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure

Frontiers in genetics, 2022-06, Vol.13, p.875013-875013

2022

Volltextzugriff (PDF)

Dachshund Homolog 1: Unveiling Its Potential Role in Megakaryopoiesis and Bacillus anthracis Lethal Toxin-Induced Thrombocytopenia

International journal of molecular sciences, 2024-03, Vol.25 (6), p.3102

2024

Volltextzugriff (PDF)

Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome

Npj genomic medicine, 2021-08, Vol.6 (1), p.68-68, Article 68

2021

Volltextzugriff (PDF)

Generation and analysis of a mouse model of pseudohypoaldosteronism type II caused by KLHL3 mutation in BTB domain

The FASEB journal, 2019-01, Vol.33 (1), p.1051-1061

2019

Volltextzugriff (PDF)

Phosphorylation Regulates NCC Stability and Transporter Activity In Vivo

Journal of the American Society of Nephrology, 2013-10, Vol.24 (10), p.1587-1597

2013

Volltextzugriff (PDF)

Genotype, Phenotype, and Follow-Up in Taiwanese Patients with Salt-Losing Tubulopathy Associated with SLC12A3 Mutation

The journal of clinical endocrinology and metabolism, 2012-08, Vol.97 (8), p.E1478-E1482

2012

Volltextzugriff (PDF)

Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia

Scientific reports, 2017-11, Vol.7 (1), p.15337-10, Article 15337

2017

Volltextzugriff (PDF)

Recurrent Deep Intronic Mutations in the SLC12A3 Gene Responsible for Gitelman's Syndrome

Clinical journal of the American Society of Nephrology, 2011-03, Vol.6 (3), p.630-639

2011

Volltextzugriff (PDF)

Nonketotic Hyperglycinemia of Infants in Taiwan

Pediatrics and neonatology, 2016-10, Vol.57 (5), p.420-426

2016

Volltextzugriff (PDF)

Chronic Metabolic Acidosis Activates Renal Tubular Sodium Chloride Cotransporter through Angiotension II-dependent WNK4-SPAK Phosphorylation Pathway

Scientific reports, 2016-01, Vol.6 (1), p.18360-18360, Article 18360

2016

Volltextzugriff (PDF)

A neonate with recurrent tetany: questions

Pediatric nephrology (Berlin, West), 2016-05, Vol.31 (5), p.753-753

2016

Volltextzugriff (PDF)

A neonate with recurrent tetany: Answers

Pediatric nephrology (Berlin, West), 2016-05, Vol.31 (5), p.755-757

2016

Volltextzugriff (PDF)

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis

Clinica chimica acta, 2012-12, Vol.414, p.105-108

2012

Volltextzugriff (PDF)

Hyponatremia is a surrogate marker of poor outcome in peritoneal dialysis-related peritonitis

BMC nephrology, 2014-07, Vol.15 (1), p.113-113, Article 113

2014

Volltextzugriff (PDF)

Artificial Intelligence-Assisted Electrocardiography for Early Diagnosis of Thyrotoxic Periodic Paralysis: PO1137

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.374-374

2021

Volltextzugriff (PDF)

Routledge Handbook of Democratization in East Asia

1st edition., 2017

Volltextzugriff (PDF)

Novel KCNJ1 Mutations Responsible for Adult Bartter Syndrome With Hypocalcemia: SA-PO569

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.761-761

2022

Volltextzugriff (PDF)

Recurrent SLC12A3 Mutations in Taiwanese Families with Gitelman Syndrome: A Rapid Detection for the Higher Prevalence: PO1622

Journal of the American Society of Nephrology, 2020-10, Vol.31 (10S), p.514-514

2020

Volltextzugriff (PDF)

Phase III HEAT Study Adding Lyso-Thermosensitive Liposomal Doxorubicin to Radiofrequency Ablation in Patients with Unresectable Hepatocellular Carcinoma Lesions

Clinical cancer research, 2018-01, Vol.24 (1), p.73-83

2018

Volltextzugriff (PDF)

Dachshund Homolog 1: Unveiling Its Potential Role in Megakaryopoiesis and IBacillus anthracis/I Lethal Toxin-Induced Thrombocytopenia

International journal of molecular sciences, 2024-03, Vol.25 (6)

2024

Volltextzugriff (PDF)

Intrusion Response Mobile Firewall Design in Ad Hoc Networks and Based on SMP Performance Analysis

Applied Mechanics and Materials, 2014-01, Vol.496-500 (Frontiers of Manufacturing and Design Science IV), p.1909-1914

2014

Volltextzugriff (PDF)

A neonate with recurrent tetany: questions and answers

Pediatric nephrology (Berlin, West), 2016-05, Vol.31 (5), p.753, 755-753

2016

Volltextzugriff (PDF)

Dynamic Modeling and Evaluating of Moving Object Tracking with Correlated Measuring Noises

Applied Mechanics and Materials, 2012-01, Vol.121-126, p.2666-2670

2012

Volltextzugriff (PDF)

1 – 24 von 24

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(23)
Mit Volltextzugriff
(23)

Publikationsform

Artikel
(23)
Bücher
(1)

Sprache

Englisch
(24)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Bartonella infection in shelter cats and dogs and their ectoparasites

Novel CNNM2 Mutation Responsible for Autosomal-Dominant Hypomagnesemia With Seizure

Dachshund Homolog 1: Unveiling Its Potential Role in Megakaryopoiesis and Bacillus anthracis Lethal Toxin-Induced Thrombocytopenia

Allele-specific RT-PCR for the rapid detection of recurrent SLC12A3 mutations for Gitelman syndrome

Generation and analysis of a mouse model of pseudohypoaldosteronism type II caused by KLHL3 mutation in BTB domain

Phosphorylation Regulates NCC Stability and Transporter Activity In Vivo

Genotype, Phenotype, and Follow-Up in Taiwanese Patients with Salt-Losing Tubulopathy Associated with SLC12A3 Mutation

Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia

Recurrent Deep Intronic Mutations in the SLC12A3 Gene Responsible for Gitelman's Syndrome

Nonketotic Hyperglycinemia of Infants in Taiwan

Chronic Metabolic Acidosis Activates Renal Tubular Sodium Chloride Cotransporter through Angiotension II-dependent WNK4-SPAK Phosphorylation Pathway

A neonate with recurrent tetany: questions

A neonate with recurrent tetany: Answers

Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis

Hyponatremia is a surrogate marker of poor outcome in peritoneal dialysis-related peritonitis

Artificial Intelligence-Assisted Electrocardiography for Early Diagnosis of Thyrotoxic Periodic Paralysis: PO1137

Routledge Handbook of Democratization in East Asia

Novel KCNJ1 Mutations Responsible for Adult Bartter Syndrome With Hypocalcemia: SA-PO569

Recurrent SLC12A3 Mutations in Taiwanese Families with Gitelman Syndrome: A Rapid Detection for the Higher Prevalence: PO1622

Phase III HEAT Study Adding Lyso-Thermosensitive Liposomal Doxorubicin to Radiofrequency Ablation in Patients with Unresectable Hepatocellular Carcinoma Lesions

Dachshund Homolog 1: Unveiling Its Potential Role in Megakaryopoiesis and IBacillus anthracis/I Lethal Toxin-Induced Thrombocytopenia

Intrusion Response Mobile Firewall Design in Ad Hoc Networks and Based on SMP Performance Analysis

A neonate with recurrent tetany: questions and answers

Dynamic Modeling and Evaluating of Moving Object Tracking with Correlated Measuring Noises

Suchergebnisse filtern