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Browsing publications by
Dr Eugen-Matthias Strehle
Newcastle Authors
Title
Year
Full text
Dr Eugen-Matthias Strehle
REVEAL-CP: Selective Screening of Pediatric Patients for Aromatic L-Amino Acid Decarboxylase Deficiency with a Guthrie Card and In Silico Structural Modeling of One Index Case
2025
Dr Eugen-Matthias Strehle
Acute kidney injury after treatment of paracetamol overdose using N-acetylcysteine guideline
2023
Dr Eugen-Matthias Strehle
Freiherr von Münchhausen and the two syndromes bearing his name
2023
Dr Eugen-Matthias Strehle
From Munchausen syndrome by proxy to factitious disorder imposed on another: What's in a name?
2023
Dr Eugen-Matthias Strehle
Opportunities to improve screening programmes identifying patients with aromatic L-amino acid decarboxylase deficiency (AADCd) in the UK
2023
Dr Eugen-Matthias Strehle
Lorelle Dismore
Child Health Innovation - YouTube
2021
Dr Eugen-Matthias Strehle
Imaging of Children with a Urinary Tract Infection in North East England
2021
Dr Eugen-Matthias Strehle
Dr Sarah Hill
Physicians' adherence to published guidelines regarding the outpatient care of pediatric patients with neurofibromatosis type 1
2020
Dr Eugen-Matthias Strehle
Professor Judith Rankin
A survey of health care professionals' knowledge and experience of foetal alcohol spectrum disorder and alcohol use in pregnancy
2019
Dr Eugen-Matthias Strehle
New ways of preventing vitamin K deficiency bleeding in infancy
2019
Dr Eugen-Matthias Strehle
Professor Judith Rankin
A survey of health care professionals' knowledge and experience of fetal alcohol spectrum disorder (FASD) and alcohol use in pregnancy
2018
Professor Judith Rankin
Dr Eugen-Matthias Strehle
Assessing prevalence of alcohol consumption in early pregnancy: Self-report compared to blood biomarker analysis
2018
Dr Eugen-Matthias Strehle
The Era of Omics and Personalized Medicine
2017
Dr Eugen-Matthias Strehle
Dr Katherine Johnson
Professor Volker Straub
Two novel mutations in the
FHL1
gene extending the phenotypic spectrum
2017
Dr Eugen-Matthias Strehle
A virtual genetics clinic on 4q deletion syndrome
2016
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