UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 116

Sortiert nach

Fungi in archives, libraries, and museums: a review on paper conservation and human health

Critical reviews in microbiology, 2019-11, Vol.45 (5-6), p.686-700

2019

Volltextzugriff (PDF)

Iron-gall inks: a review of their degradation mechanisms and conservation treatments

Heritage science, 2022-09, Vol.10 (1), p.1-11, Article 145

2022

Volltextzugriff (PDF)

Improving access: Multi-analytical survey of the Norwegian Sea trade archive to establish storage conditions, digitisation priorities and conservation treatments

Journal of cultural heritage, 2024-07, Vol.68, p.47-58

2024

Volltextzugriff (PDF)

Microbial Assessment in A Rare Norwegian Book Collection: A One Health Approach to Cultural Heritage

Microorganisms (Basel), 2024-06, Vol.12 (6), p.1215

2024

Volltextzugriff (PDF)

Cleaning fungal stains on paper with hydrogels: The effect of pH control

International biodeterioration & biodegradation, 2020-08, Vol.152, p.104996, Article 104996

2020

Volltextzugriff (PDF)

Characterization of Fungal Melanins from Black Stains on Paper Artefacts

Heritage, 2022-12, Vol.5 (4), p.3049-3065

2022

Volltextzugriff (PDF)

Clotrimazole and calcium hydroxide nanoparticles: A low toxicity antifungal alternative for paper conservation

Journal of cultural heritage, 2017-03, Vol.24, p.45-52

2017

Volltextzugriff (PDF)

Study of the Materials and Techniques of a Rare Papier-Mâché Mushroom Model Crafted in H. Arnoldi Factory

Molecules (Basel, Switzerland), 2023-01, Vol.28 (3), p.1062

2023

Volltextzugriff (PDF)

4-MUF-NAG for fungal biomass determination: Scope and limitations in the context of biodeterioration studies

Journal of cultural heritage, 2016-11, Vol.22, p.992-998

2016

Volltextzugriff (PDF)

Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.298-298, Article 298

2020

Volltextzugriff (PDF)

Combining an innovative non-invasive sampling method and high-throughput sequencing to characterize fungal communities on a canvas painting

International biodeterioration & biodegradation, 2019-11, Vol.145, p.104816, Article 104816

2019

Volltextzugriff (PDF)

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis

Nature genetics, 2018-01, Vol.50 (1), p.120-129

2018

Volltextzugriff (PDF)

eP210: A rare case of familial syndromic intellectual disability: First reported Portuguese patients

Genetics in medicine, 2022-03, Vol.24 (3), p.S131-S132

2022

Volltextzugriff (PDF)

Congenital Disorders of Glycosylation in Portugal—Two Decades of Experience

The Journal of pediatrics, 2021-04, Vol.231, p.148-156

2021

Volltextzugriff (PDF)

Hyperprolinemia as a clue in the diagnosis of a patient with psychiatric manifestations

Brain & development (Tokyo. 1979), 2017-06, Vol.39 (6), p.539-541

2017

Volltextzugriff (PDF)

Fungal Biodeterioration of Paper: How are Paper and Book Conservators Dealing with it? An International Survey

Restaurator, 2014, Vol.35 (2), p.181-199

2014

Volltextzugriff (PDF)

Sulfite oxidase deficiency – An unusual late and mild presentation

Brain & development (Tokyo. 1979), 2014-02, Vol.36 (2), p.176-179

2014

Volltextzugriff (PDF)

MEGDEL Syndrome: Expanding the Phenotype and New Mutations

Neuropediatrics, 2017-10, Vol.48 (5), p.382

2017

Volltextzugriff (PDF)

Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal

Frontiers in genetics, 2023-04, Vol.13, p.1088040-1088040

2023

Volltextzugriff (PDF)

Unraveling the genetic background of individuals with a clinical familial hypercholesterolemia phenotype

Journal of lipid research, 2024-02, Vol.65 (2), p.100490-100490, Article 100490

2024

Volltextzugriff (PDF)

Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type

Molecular genetics and metabolism, 2008-04, Vol.93 (4), p.475-480

2008

Volltextzugriff (PDF)

Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome

CEN case reports, 2018-05, Vol.7 (1), p.73-76

2018

Volltextzugriff (PDF)

Pompe Disease and Normal Whole-Body Magnetic Resonance Imaging

Journal of neuromuscular diseases, 2015, Vol.2 (s1), p.S12-S12

2015

Volltextzugriff (PDF)

Phenylketonuria in Portugal: Genotype–phenotype correlations using molecular, biochemical, and haplotypic analyses

Molecular genetics & genomic medicine, 2021-03, Vol.9 (3), p.e1559-n/a

2021

Volltextzugriff (PDF)

1 – 25 von 116

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(108)
Mit Volltextzugriff
(111)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Fungi in archives, libraries, and museums: a review on paper conservation and human health

Iron-gall inks: a review of their degradation mechanisms and conservation treatments

Improving access: Multi-analytical survey of the Norwegian Sea trade archive to establish storage conditions, digitisation priorities and conservation treatments

Microbial Assessment in A Rare Norwegian Book Collection: A One Health Approach to Cultural Heritage

Cleaning fungal stains on paper with hydrogels: The effect of pH control

Characterization of Fungal Melanins from Black Stains on Paper Artefacts

Clotrimazole and calcium hydroxide nanoparticles: A low toxicity antifungal alternative for paper conservation

Study of the Materials and Techniques of a Rare Papier-Mâché Mushroom Model Crafted in H. Arnoldi Factory

4-MUF-NAG for fungal biomass determination: Scope and limitations in the context of biodeterioration studies

Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients

Combining an innovative non-invasive sampling method and high-throughput sequencing to characterize fungal communities on a canvas painting

Mutations in SELENBP1, encoding a novel human methanethiol oxidase, cause extraoral halitosis

eP210: A rare case of familial syndromic intellectual disability: First reported Portuguese patients

Congenital Disorders of Glycosylation in Portugal—Two Decades of Experience

Hyperprolinemia as a clue in the diagnosis of a patient with psychiatric manifestations

Fungal Biodeterioration of Paper: How are Paper and Book Conservators Dealing with it? An International Survey

Sulfite oxidase deficiency – An unusual late and mild presentation

Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction

MEGDEL Syndrome: Expanding the Phenotype and New Mutations

Rare primary dyslipidaemias associated with low LDL and HDL cholesterol values in Portugal

Unraveling the genetic background of individuals with a clinical familial hypercholesterolemia phenotype

Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type

Atypical adult-onset methylmalonic acidemia and homocystinuria presenting as hemolytic uremic syndrome

Pompe Disease and Normal Whole-Body Magnetic Resonance Imaging

Phenylketonuria in Portugal: Genotype–phenotype correlations using molecular, biochemical, and haplotypic analyses

Suchergebnisse filtern