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...

A novel mutation of adenosine deaminase causing SCID presenting as hemophagocytic lymphohistiocytosis with acute kidney injury

British journal of haematology, 2020-11, Vol.191 (3), p.509-512

2020

Volltextzugriff (PDF)

Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1696-1700

2021

Volltextzugriff (PDF)

Is oral levothyroxine as effective as its intravenous form in myxoedema crisis with catecholamine‐refractory shock?

Journal of paediatrics and child health, 2022-04, Vol.58 (4), p.717-718

2022

Volltextzugriff (PDF)

Miliary nodules with recurrent air leaks in a child: A mystery

Journal of paediatrics and child health, 2022-03, Vol.58 (3), p.516-518

2022

Volltextzugriff (PDF)

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Questions

Pediatric nephrology (Berlin, West), 2020-12, Vol.35 (12), p.2275-2277

2020

Volltextzugriff (PDF)

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Answers

Pediatric nephrology (Berlin, West), 2020-12, Vol.35 (12), p.2279-2283

2020

Volltextzugriff (PDF)

Soap bubble appearance: an ominous sign

BMJ case reports, 2019-05, Vol.12 (5), p.e229721

2019

Volltextzugriff (PDF)

MRI findings in a child with neuromelioidosis

Neurology, 2020-11, Vol.95 (18), p.836-837

2020

Volltextzugriff (PDF)

A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant

Indian Pediatrics Case Reports, 2024-07, Vol.4 (3), p.173-177

2024

Volltextzugriff (PDF)

Trial of Furosemide to Prevent Acute Kidney Injury in Critically Ill Children: A Double-Blind, Randomized, Controlled Trial

Indian journal of pediatrics, 2021-11, Vol.88 (11), p.1099-1106

2021

Volltextzugriff (PDF)

Epinephrine Plus Vasopressin vs Epinephrine Plus Placebo in Pediatric Intensive Care Unit Cardiopulmonary Resuscitation: A Randomized Double Blind Controlled Clinical Trial

Indian pediatrics, 2021-07, Vol.58 (7), p.624-630

2021

Volltextzugriff (PDF)

Cerebral sinus venous thrombosis: a rare complication of varicella infection in a 12-year-old girl

Paediatrics and international child health, 2022-10, Vol.42 (3-4), p.1-168

2022

Volltextzugriff (PDF)

Microcephaly in infantile Sandhoff's disease

BMJ case reports, 2017-06, Vol.2017, p.bcr-2017-220912

2017

Volltextzugriff (PDF)

A novel mutation of adenosine deaminase causing SCID presenting as hemophagocytic lymphohistiocytosis with acute kidney injury

British journal of haematology, 2020, Vol.191 (3), p.509-512

2020

Volltextzugriff (PDF)

Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome

Journal of clinical immunology, 2021, Vol.41 (7), p.1696-1700

2021

Volltextzugriff (PDF)

Is oral levothyroxine as effective as its intravenous form in myxoedema crisis with catecholamine-refractory shock?

Journal of paediatrics and child health, 2022, Vol.58 (4), p.717-718

2022

Volltextzugriff (PDF)

Miliary nodules with recurrent air leaks in a child: A mystery

Journal of paediatrics and child health, 2022, Vol.58 (3), p.516-518

2022

Volltextzugriff (PDF)

3D QSAR and Molecular Docking Studies of Benzimidazole Derivatives as Hepatitis C Virus NS5B Polymerase Inhibitors

Journal of chemical information and modeling, 2008-01, Vol.48 (1), p.42-55

2008

Volltextzugriff (PDF)

Structure-based virtual screening, synthesis and SAR of novel inhibitors of hepatitis C virus NS5B polymerase

Bioorganic & medicinal chemistry, 2010-07, Vol.18 (13), p.4630-4638

2010

Volltextzugriff (PDF)

Design and synthesis of l- and d-phenylalanine derived rhodanines with novel C5-arylidenes as inhibitors of HCV NS5B polymerase

Bioorganic & medicinal chemistry, 2013-06, Vol.21 (11), p.3262-3271

2013

Volltextzugriff (PDF)

Synthesis and SAR optimization of diketo acid pharmacophore for HCV NS5B polymerase inhibition

European journal of medicinal chemistry, 2011-10, Vol.46 (10), p.5138-5145

2011

Volltextzugriff (PDF)

The INPHOG childhood cancer survivorship (C2S) study: Progress & challenges

Pediatric hematology oncology journal, 2023, Vol.8 (4), p.S12

2023

Volltextzugriff (PDF)

Friedreich’s ataxia associated with marfanoid features & alopecia areata-rare disease manifestations or chance association?

Indian journal of medical specialities, 2017-10, Vol.8 (4), p.200-202

2017

Volltextzugriff (PDF)

Neuromyelitis optica spectrum disorders: An experience from tertiary care hospital of North–West India

Indian journal of medical specialities, 2017-10, Vol.8 (4), p.192-196

2017

Volltextzugriff (PDF)

CMA—H∞ Hybrid Design of Robust Stable Adaptive Fuzzy Controllers for Non-linear Systems

Operations Research and Optimization, p.145-155

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(21)
Mit Volltextzugriff
(26)

Publikationsform

Sprache

Englisch
(30)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(17)
Science & Technology
(17)
Humans
(9)
Pediatrics
(8)
Chemistry, Medicinal
(4)
Child
(4)
Medicine
(4)
Medicine & Public Health
(4)
Pharmacology & Pharmacy
(4)
Viral Nonstructural Proteins - Antagonists & Inhibitors
(4)
Antiviral Agents - Chemical Synthesis
(3)
Antiviral Agents - Chemistry
(3)
Case Reports
(3)
Chemistry
(3)
Children
(3)
Female
(3)
General & Internal Medicine
(3)
Hepacivirus - Enzymology
(3)
Infant
(3)
Medicine, General & Internal
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

A novel mutation of adenosine deaminase causing SCID presenting as hemophagocytic lymphohistiocytosis with acute kidney injury

Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome

Is oral levothyroxine as effective as its intravenous form in myxoedema crisis with catecholamine‐refractory shock?

Miliary nodules with recurrent air leaks in a child: A mystery

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Questions

Severe acute kidney injury in a 3-year-old boy with fever and pleural effusion: Answers

Soap bubble appearance: an ominous sign

MRI findings in a child with neuromelioidosis

A Rare Compound Heterozygous Mutation of TRPM6 Gene in Hereditary Hypomagnesemia with Secondary Hypocalcemia: A Cause of Refractory Seizures in an Infant

Trial of Furosemide to Prevent Acute Kidney Injury in Critically Ill Children: A Double-Blind, Randomized, Controlled Trial

Epinephrine Plus Vasopressin vs Epinephrine Plus Placebo in Pediatric Intensive Care Unit Cardiopulmonary Resuscitation: A Randomized Double Blind Controlled Clinical Trial

Cerebral sinus venous thrombosis: a rare complication of varicella infection in a 12-year-old girl

Microcephaly in infantile Sandhoff's disease

A novel mutation of adenosine deaminase causing SCID presenting as hemophagocytic lymphohistiocytosis with acute kidney injury

Macrophage Activation Syndrome in a Patient with Prolidase Deficiency: a Rare Genetic Disorder Associated with Elevated IgE and Lupus-Like Syndrome

Is oral levothyroxine as effective as its intravenous form in myxoedema crisis with catecholamine-refractory shock?

Miliary nodules with recurrent air leaks in a child: A mystery

3D QSAR and Molecular Docking Studies of Benzimidazole Derivatives as Hepatitis C Virus NS5B Polymerase Inhibitors

Structure-based virtual screening, synthesis and SAR of novel inhibitors of hepatitis C virus NS5B polymerase

Design and synthesis of l- and d-phenylalanine derived rhodanines with novel C5-arylidenes as inhibitors of HCV NS5B polymerase

Synthesis and SAR optimization of diketo acid pharmacophore for HCV NS5B polymerase inhibition

The INPHOG childhood cancer survivorship (C2S) study: Progress & challenges

Friedreich’s ataxia associated with marfanoid features & alopecia areata-rare disease manifestations or chance association?

Neuromyelitis optica spectrum disorders: An experience from tertiary care hospital of North–West India

CMA—H∞ Hybrid Design of Robust Stable Adaptive Fuzzy Controllers for Non-linear Systems

Suchergebnisse filtern