UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 163

Sortiert nach

Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val

Acta neurologica Scandinavica, 2016-05, Vol.133 (5), p.361-366

2016

Link zum Volltext

Verfügbarkeit prüfen

Primary familial brain calcification linked to deletion of 5’ noncoding region of SLC20A2

Acta neurologica Scandinavica, 2017-07, Vol.136 (1), p.59-63

2017

Link zum Volltext

Verfügbarkeit prüfen

Neuroimaging and neurological outcome of children with acute encephalitis

Developmental medicine and child neurology, 2022-10, Vol.64 (10), p.1262-1269

2022

Link zum Volltext

Verfügbarkeit prüfen

Decreased bone mineral density and content in neurofibromatosis. type 1: Lowest local values are located in the load-carrying parts of the body

Osteoporosis international, 2005-08, Vol.16 (8), p.928-936

2005

Link zum Volltext

Verfügbarkeit prüfen

The effect of dietary counselling on food intakes in pregnant women at risk for gestational diabetes: a secondary analysis of a randomised controlled trial RADIEL

European journal of clinical nutrition, 2016-08, Vol.70 (8), p.912-917

2016

Link zum Volltext

Verfügbarkeit prüfen

APOE and AGT in the Finnish p.Arg133Cys CADASIL population

Acta neurologica Scandinavica, 2015-12, Vol.132 (6), p.430-434

2015

Link zum Volltext

Verfügbarkeit prüfen

A prospective, randomized study of goal-oriented hemodynamic therapy in cardiac surgical patients

Anesthesia and analgesia, 2000-05, Vol.90 (5), p.1052-1059

2000

Link zum Volltext

Verfügbarkeit prüfen

The effect of carbon dioxide, respiratory rate and tidal volume on human heart rate variability

Acta anaesthesiologica Scandinavica, 2004-01, Vol.48 (1), p.93-101

2004

Link zum Volltext

Verfügbarkeit prüfen

A clinical assessment of neurofibromatosis type 1 (NF1) and segmental NF in northern Finland

Journal of medical genetics, 2000-12, Vol.37 (12), p.e43-43

POYHONEN, M

2000

Link zum Volltext

Verfügbarkeit prüfen

Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)

Neurology, 2002-09, Vol.59 (5), p.759

2002

Link zum Volltext

Verfügbarkeit prüfen

Effects of sympatholytic therapy on postmenopausal symptoms in hypertensive postmenopausal women

Climacteric : the journal of the International Menopause Society, 2014-08, Vol.17 (4), p.356-362

2014

Link zum Volltext

Verfügbarkeit prüfen

Cardiorespiratory fitness and health‐related quality of life in women at risk for gestational diabetes

Scandinavian journal of medicine & science in sports, 2018-01, Vol.28 (1), p.203-211

2018

Link zum Volltext

Verfügbarkeit prüfen

Neurofibromatosis type 1 gene mutation analysis using sequence capture and high-throughput sequencing

Acta dermato-venereologica, 2014-01, Vol.94 (6), p.663-666

2014

Link zum Volltext

Verfügbarkeit prüfen

Molecular analysis of astrocytomas presenting after age 10 in individuals with NF1

Neurology, 2003-11, Vol.61 (10), p.1397

2003

Link zum Volltext

Verfügbarkeit prüfen

CADASIL and CARASIL

Brain pathology (Zurich, Switzerland), 2014-09, Vol.24 (5), p.525-544

2014

Link zum Volltext

Verfügbarkeit prüfen

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Nature medicine, 1998-04, Vol.4 (4), p.452-455

1998

Link zum Volltext

Verfügbarkeit prüfen

Loss of SUFU Function in Familial Multiple Meningioma

American journal of human genetics, 2012-09, Vol.91 (3), p.520-526

2012

Link zum Volltext

Verfügbarkeit prüfen

Molecular genetic and clinical findings in identical twins with CADASIL

JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, Vol.283 (1), p.294-294

2009

Link zum Volltext

Verfügbarkeit prüfen

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Frontiers in immunology, 2019-12, Vol.10, p.2770-2770

2019

Link zum Volltext

Verfügbarkeit prüfen

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Brain (London, England : 1878), 2009-04, Vol.132 (4), p.933-939

2009

Link zum Volltext

Verfügbarkeit prüfen

Genetic factors modify the clinical course of CADASIL

JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, Vol.283 (1), p.294-294

2009

Link zum Volltext

Verfügbarkeit prüfen

Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL

JOURNAL OF THE NEUROLOGICAL SCIENCES, 2009, Vol.283 (1), p.293-294

2009

Link zum Volltext

Verfügbarkeit prüfen

Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

American journal of human genetics, 1998-06, Vol.62 (6), p.1544-1548

1998

Link zum Volltext

Verfügbarkeit prüfen

On the convergence of multiattribute weighting methods

European journal of operational research, 2001-03, Vol.129 (3), p.569-585

2001

Link zum Volltext

Verfügbarkeit prüfen

Insulin resistance without coexisting hyperglycaemia is not independently associated with cardiorespiratory fitness or its components in women

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 163

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(142)
Mit Volltextzugriff
(140)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val

Primary familial brain calcification linked to deletion of 5’ noncoding region of SLC20A2

Neuroimaging and neurological outcome of children with acute encephalitis

Decreased bone mineral density and content in neurofibromatosis. type 1: Lowest local values are located in the load-carrying parts of the body

The effect of dietary counselling on food intakes in pregnant women at risk for gestational diabetes: a secondary analysis of a randomised controlled trial RADIEL

APOE and AGT in the Finnish p.Arg133Cys CADASIL population

A prospective, randomized study of goal-oriented hemodynamic therapy in cardiac surgical patients

The effect of carbon dioxide, respiratory rate and tidal volume on human heart rate variability

A clinical assessment of neurofibromatosis type 1 (NF1) and segmental NF in northern Finland

Gliomas presenting after age 10 in individuals with neurofibromatosis type 1 (NF1)

Effects of sympatholytic therapy on postmenopausal symptoms in hypertensive postmenopausal women

Cardiorespiratory fitness and health‐related quality of life in women at risk for gestational diabetes

Neurofibromatosis type 1 gene mutation analysis using sequence capture and high-throughput sequencing

Molecular analysis of astrocytomas presenting after age 10 in individuals with NF1

CADASIL and CARASIL

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Loss of SUFU Function in Familial Multiple Meningioma

Molecular genetic and clinical findings in identical twins with CADASIL

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

Genetic factors modify the clinical course of CADASIL

Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL

Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

On the convergence of multiattribute weighting methods

Insulin resistance without coexisting hyperglycaemia is not independently associated with cardiorespiratory fitness or its components in women

Suchergebnisse filtern