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...

Notes from the field: Measles outbreaks from imported cases in Orthodox Jewish communities — New York and New Jersey, 2018–2019

American journal of transplantation, 2019-07, Vol.19 (7), p.2131-2133

2019

Volltextzugriff (PDF)

Measles Outbreaks from Imported Cases in Orthodox Jewish Communities — New York and New Jersey, 2018–2019

MMWR. Morbidity and mortality weekly report, 2019, Vol.68 (19), p.444-445

2019

Volltextzugriff (PDF)

Notes from the Field: Measles Outbreaks from Imported Cases in Orthodox Jewish Communities - New York and New Jersey, 2018-2019

MMWR. Morbidity and mortality weekly report, 2019-05, Vol.68 (19), p.444-445

2019

Volltextzugriff (PDF)

Measles Outbreaks from Imported Cases in Orthodox Jewish Communities - New York and New Jersey, 2018–2019

MMWR. Morbidity and Mortality Weekly Report, 2019, Vol.68 (19), p.444-445

2019

Volltextzugriff (PDF)

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

Human molecular genetics, 2008-12, Vol.17 (23), p.3631-3642

2008

Volltextzugriff (PDF)

Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations

Journal of neuropathology and experimental neurology, 2007-02, Vol.66 (2), p.142-151

2007

Volltextzugriff (PDF)

Effectiveness of smoking cessation interventions among adults: an overview of systematic reviews

Systematic reviews, 2024-07, Vol.13 (1), p.179-33, Article 179

2024

Volltextzugriff (PDF)

An investigation into the accuracy of using serum creatinine estimated glomerular filtration rate to predict measured glomerular filtration rate

Nuclear medicine communications, 2019-04, Vol.40 (4), p.349-352

2019

Volltextzugriff (PDF)

Atypical Progressive Supranuclear Palsy With Corticospinal Tract Degeneration

Journal of neuropathology and experimental neurology, 2006-04, Vol.65 (4), p.396-405

2006

Volltextzugriff (PDF)

Prominent phenotypic variability associated with mutations in Progranulin

Neurobiology of aging, 2009-05, Vol.30 (5), p.739-751

2009

Volltextzugriff (PDF)

Cost-effectiveness of Aflibercept Monotherapy vs Bevacizumab First Followed by Aflibercept If Needed for Diabetic Macular Edema

JAMA ophthalmology, 2023-03, Vol.141 (3), p.268

2023

Volltextzugriff (PDF)

Mutations in progranulin explain atypical phenotypes with variants in MAPT

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3124-3126

2006

Volltextzugriff (PDF)

Control of growth hormone and IGF1 in patients with acromegaly in the UK: responses to medical treatment with somatostatin analogues and dopamine agonists

Clinical endocrinology (Oxford), 2013-11, Vol.79 (5), p.689-699

2013

Volltextzugriff (PDF)

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Human molecular genetics, 2006-10, Vol.15 (20), p.2988-3001

2006

Volltextzugriff (PDF)

Frontotemporal dementia and parkinsonism associated with the IVS1+1G→A mutation in progranulin: a clinicopathologic study

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3103-3114

2006

Volltextzugriff (PDF)

Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)

Parkinsonism & related disorders, 2007-05, Vol.13 (4), p.230-239

2007

Volltextzugriff (PDF)

A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch

Neurobiology of disease, 2002-03, Vol.9 (2), p.269-273

2002

Volltextzugriff (PDF)

The Effect of tau genotype on clinical features in FTDP-17

Parkinsonism & related disorders, 2005-06, Vol.11 (4), p.205-208

2005

Volltextzugriff (PDF)

Familial frontotemporal dementia associated with a novel presenilin-1 mutation

Dementia and geriatric cognitive disorders, 2002-01, Vol.14 (1), p.13-21

2002

Volltextzugriff (PDF)

Effects of Sudden Infant Death on Bereaved Siblings; a Comparative Study

Journal of child psychology and psychiatry, 1994-05, Vol.35 (4), p.723-732

1994

Volltextzugriff (PDF)

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin

Archives of neurology (Chicago), 2010-02, Vol.67 (2), p.171

2010

Volltextzugriff (PDF)

Late-onset frontotemporal dementia associated with progressive supranuclear palsy/argyrophilic grain disease/Alzheimer's disease pathology

Neurocase, 2005-06, Vol.11 (3), p.204-211

2005

Volltextzugriff (PDF)

Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathology

Dementia and geriatric cognitive disorders, 2002-01, Vol.13 (2), p.80-90

2002

Volltextzugriff (PDF)

1 – 25 von 30

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(26)
Mit Volltextzugriff
(24)

Publikationsform

Sprache

Englisch
(30)

Erscheinungsjahr

n.n

Thema

Science & Technology
(23)
Life Sciences & Biomedicine
(21)
Humans
(19)
Middle Aged
(15)
Male
(14)
Female
(13)
Dementia - Genetics
(12)
Aged
(11)
Neurosciences & Neurology
(11)
Biological And Medical Sciences
(10)
Mutation
(10)
Clinical Neurology
(9)
Neurology
(9)
Aged, 80 And Over
(7)
Frontotemporal Dementia
(7)
Intercellular Signaling Peptides And Proteins - Genetics
(7)
Medical Sciences
(7)
Adult
(6)
Phenotype
(6)
Dementia - Metabolism
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Notes from the field: Measles outbreaks from imported cases in Orthodox Jewish communities — New York and New Jersey, 2018–2019

Measles Outbreaks from Imported Cases in Orthodox Jewish Communities — New York and New Jersey, 2018–2019

Notes from the Field: Measles Outbreaks from Imported Cases in Orthodox Jewish Communities - New York and New Jersey, 2018-2019

Measles Outbreaks from Imported Cases in Orthodox Jewish Communities - New York and New Jersey, 2018–2019

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

Neuropathologic Features of Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions With Progranulin Gene (PGRN) Mutations

Effectiveness of smoking cessation interventions among adults: an overview of systematic reviews

An investigation into the accuracy of using serum creatinine estimated glomerular filtration rate to predict measured glomerular filtration rate

Patient stratification using plasma cytokines and their regulators in sepsis: relationship to outcomes, treatment effect and leucocyte transcriptomic subphenotypes

Atypical Progressive Supranuclear Palsy With Corticospinal Tract Degeneration

Prominent phenotypic variability associated with mutations in Progranulin

Cost-effectiveness of Aflibercept Monotherapy vs Bevacizumab First Followed by Aflibercept If Needed for Diabetic Macular Edema

Mutations in progranulin explain atypical phenotypes with variants in MAPT

Control of growth hormone and IGF1 in patients with acromegaly in the UK: responses to medical treatment with somatostatin analogues and dopamine agonists

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Frontotemporal dementia and parkinsonism associated with the IVS1+1G→A mutation in progranulin: a clinicopathologic study

Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)

A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch

The Effect of tau genotype on clinical features in FTDP-17

Familial frontotemporal dementia associated with a novel presenilin-1 mutation

Effects of Sudden Infant Death on Bereaved Siblings; a Comparative Study

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin

Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis: e1000193

Late-onset frontotemporal dementia associated with progressive supranuclear palsy/argyrophilic grain disease/Alzheimer's disease pathology

Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathology

Suchergebnisse filtern