UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 38

Sortiert nach

Virtual visits at the Helsinki Head and Neck Center during the COVID-19 pandemic: patient safety incidents and the experiences of patients and staff

BMC health services research, 2023-05, Vol.23 (1), p.483-483, Article 483

2023

Volltextzugriff (PDF)

Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations

Ophthalmology (Rochester, Minn.), 2016-07, Vol.123 (7), p.1624-1626

2016

Volltextzugriff (PDF)

Anterior segment optical coherence tomography in autosomal recessive cornea plana

Acta ophthalmologica (Oxford, England), 2015-05, Vol.93 (3), p.e232-e233

2015

Volltextzugriff (PDF)

Keratitis fugax hereditaria ‐ useful to consider when you have a child with non‐specific corneal findings and symptoms

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

Volltextzugriff (PDF)

Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches

European journal of human genetics : EJHG, 2019-03, Vol.27 (3), p.494-502

2019

Volltextzugriff (PDF)

Foveal thickness and its association with visual acuity in adults born preterm with very low birth weight: A two-country birth cohort study

Acta ophthalmologica (Oxford, England), 2024-05

2024

Volltextzugriff (PDF)

Childhood-Onset Leber Hereditary Optic Neuropathy—Clinical and Prognostic Insights

American journal of ophthalmology, 2023-05, Vol.249, p.99-107

2023

Volltextzugriff (PDF)

Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

Acta ophthalmologica (Oxford, England), 2022-01, Vol.100 (S267), p.n/a

2022

Volltextzugriff (PDF)

Visual function in adults born preterm with very low birth weight—A two‐country birth cohort study

Acta ophthalmologica (Oxford, England), 2024-02, Vol.102 (1), p.49-57

2024

Volltextzugriff (PDF)

Analysis of glaucoma genes in Finnish patients with juvenile open‐angle glaucoma

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

Volltextzugriff (PDF)

Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

Acta ophthalmologica (Oxford, England), 2023-03, Vol.101 (2), p.215-221

2023

Volltextzugriff (PDF)

WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression

American journal of ophthalmology, 2022-09, Vol.241, p.9-27

2022

Volltextzugriff (PDF)

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3

American journal of ophthalmology, 2020-05, Vol.213, p.217-225

2020

Volltextzugriff (PDF)

Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma

Acta ophthalmologica (Oxford, England), 2023-11, Vol.101 (7), p.797-806

2023

Volltextzugriff (PDF)

In Vivo corneal confocal microscopy study of keratoendotheliitis fugax hereditaria caused by a pathogenic variant in the NLRP3 gene

Acta ophthalmologica (Oxford, England), 2019-12, Vol.97 (S263), p.n/a

2019

Volltextzugriff (PDF)

Genetic findings in over 600 individuals with inherited retinal disorders in Finland

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

Volltextzugriff (PDF)

Mutations in subunit 6 of the F1F0‐ATP synthase cause two entirely different diseases

FEBS letters, 1997-07, Vol.412 (2), p.351-354

1997

Volltextzugriff (PDF)

Refined Staging for Chorioretinopathy in Long-Chain 3-Hydroxyacyl Coenzyme A Dehydrogenase Deficiency

Ophthalmic research, 2012-01, Vol.48 (2), p.75-81

2012

Volltextzugriff (PDF)

Diphenyleneiodonium inhibits reduction of iron-sulfur clusters in the mitochondrial NADH-ubiquinone oxidoreductase (Complex I)

The Journal of biological chemistry, 1994-08, Vol.269 (33), p.21037-21042

1994

Volltextzugriff (PDF)

The plasma membrane potential of human neutrophils. Role of ion channels and the sodium/potassium pump

Biochimica et biophysica acta, 1989-04, Vol.980 (2), p.139-145

1989

Volltextzugriff (PDF)

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

The Journal of clinical investigation, 1992-07, Vol.90 (1), p.61-66

1992

Volltextzugriff (PDF)

Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation

Neuromuscular disorders : NMD, 1996-10, Vol.6 (5), p.327-337

1996

Volltextzugriff (PDF)

Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

FEBS letters, 1991-11, Vol.292 (1), p.289-292

1991

Volltextzugriff (PDF)

Anterior segment optical coherence tomography in autosomal recessive cornea plana

Acta ophthalmologica, 2015, Vol.93 (3), p.e232-e233

2015

Volltextzugriff (PDF)

Studies on the proton-translocating NADH:ubiquinone oxidoreductases of mitochondria and Escherichia coli using the inhibitor 1,10-phenanthroline

FEBS letters, 1994-02, Vol.339 (1-2), p.142-146

1994

Volltextzugriff (PDF)

1 – 25 von 38

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(36)

Publikationsform

Artikel
(37)
Berichte
(1)

Sprache

Englisch
(38)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(24)
Life Sciences & Biomedicine
(23)
Humans
(18)
Ophthalmology
(14)
Biochemistry & Molecular Biology
(8)
Biological And Medical Sciences
(8)
Child, Preschool
(6)
Medical Sciences
(6)
Patients
(6)
Biophysics
(4)
Cell Biology
(4)
Cornea
(4)
Dna, Mitochondrial - Genetics
(4)
Mitochondria - Enzymology
(4)
Mutation
(4)
Acuity
(3)
Child
(3)
Dna, Mitochondrial - Analysis
(3)
Electron Spin Resonance Spectroscopy
(3)
Infant, Newborn
(3)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Virtual visits at the Helsinki Head and Neck Center during the COVID-19 pandemic: patient safety incidents and the experiences of patients and staff

Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations

Anterior segment optical coherence tomography in autosomal recessive cornea plana

Keratitis fugax hereditaria ‐ useful to consider when you have a child with non‐specific corneal findings and symptoms

Clinical utility gene card for: inherited optic neuropathies including next-generation sequencing-based approaches

Foveal thickness and its association with visual acuity in adults born preterm with very low birth weight: A two-country birth cohort study

Childhood-Onset Leber Hereditary Optic Neuropathy—Clinical and Prognostic Insights

Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

Visual function in adults born preterm with very low birth weight—A two‐country birth cohort study

Analysis of glaucoma genes in Finnish patients with juvenile open‐angle glaucoma

Natural history and biomarkers of retinal dystrophy caused by the biallelic TULP1 variant c.148delG

WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression

In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3

Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma

In Vivo corneal confocal microscopy study of keratoendotheliitis fugax hereditaria caused by a pathogenic variant in the NLRP3 gene

Genetic findings in over 600 individuals with inherited retinal disorders in Finland

Mutations in subunit 6 of the F1F0‐ATP synthase cause two entirely different diseases

Refined Staging for Chorioretinopathy in Long-Chain 3-Hydroxyacyl Coenzyme A Dehydrogenase Deficiency

Diphenyleneiodonium inhibits reduction of iron-sulfur clusters in the mitochondrial NADH-ubiquinone oxidoreductase (Complex I)

The plasma membrane potential of human neutrophils. Role of ion channels and the sodium/potassium pump

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia

Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-coa dehydrogenase deficiency with the G1528C mutation

Electron transfer properties of NADH: Ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

Anterior segment optical coherence tomography in autosomal recessive cornea plana

Studies on the proton-translocating NADH:ubiquinone oxidoreductases of mitochondria and Escherichia coli using the inhibitor 1,10-phenanthroline

Aktive Filter

Suchergebnisse filtern