UB Paderborn / Katalog / Suche / in CDI

MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly

American journal of neuroradiology : AJNR, 2017-08, Vol.38 (8), p.1643-1646

2017

Link zum Volltext

Verfügbarkeit prüfen

Toward understanding the genetic basis of neural tube defects

Clinical genetics, 2007-04, Vol.71 (4), p.295-310

2007

Link zum Volltext

Verfügbarkeit prüfen

Contribution of VANGL2 mutations to isolated neural tube defects

Clinical genetics, 2011-07, Vol.80 (1), p.76-82

2011

Link zum Volltext

Verfügbarkeit prüfen

Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy

American journal of neuroradiology : AJNR, 2018-06, Vol.39 (6), p.1157-1163

2018

Link zum Volltext

Verfügbarkeit prüfen

The DRY motif at work: the P2Y12 receptor case

Journal of thrombosis and haemostasis, 2014-05, Vol.12 (5), p.713-715

2014

Link zum Volltext

Verfügbarkeit prüfen

Structural Connectivity Analysis in Children with Segmental Callosal Agenesis

American journal of neuroradiology : AJNR, 2017-03, Vol.38 (3), p.639-647

2017

Link zum Volltext

Verfügbarkeit prüfen

In vitro pharmacological evaluation of multitarget thromboxane prostanoid receptor/COX-2 agents: A possible strategy to solve the cardiovascular issues of COXIBs

Atherosclerosis, 2016-09, Vol.252, p.e59-e59

2016

Link zum Volltext

Verfügbarkeit prüfen

Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations

Birth defects research. A Clinical and molecular teratology, 2015-01, Vol.103 (1), p.51-61

2015

Link zum Volltext

Verfügbarkeit prüfen

Cysteinyl-leukotriene receptor antagonists: present situation and future opportunities

Current medicinal chemistry, 2006-01, Vol.13 (26), p.3213

2006

Link zum Volltext

Verfügbarkeit prüfen

Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2

European journal of neurology, 2016-04, Vol.23 (4), p.e19-e21

2016

Link zum Volltext

Verfügbarkeit prüfen

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations

European journal of paediatric neurology, 2020-09, Vol.28, p.110-119

2020

Link zum Volltext

Verfügbarkeit prüfen

Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1

American journal of medical genetics. Part A, 2014-02, Vol.164A (2), p.495-499

2014

Link zum Volltext

Verfügbarkeit prüfen

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Journal of human genetics, 2002-06, Vol.47 (6), p.319-324

2002

Link zum Volltext

Verfügbarkeit prüfen

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly

Nature genetics, 1996-01, Vol.12 (1), p.94-96

1996

Link zum Volltext

Verfügbarkeit prüfen

Molecular and functional aspects of human cysteinyl leukotriene receptors

Pharmacological research, 2004-07, Vol.50 (1), p.1-11

Capra, Valérie

2004

Link zum Volltext

Verfügbarkeit prüfen

Leukotrienes as Mediators of Asthma

Pulmonary pharmacology & therapeutics, 2001-01, Vol.14 (1), p.3-19

2001

Link zum Volltext

Verfügbarkeit prüfen

Montelukast and cardiovascular risk in asthmatics

Atherosclerosis, 2021-08, Vol.331, p.e271-e271

2021

Link zum Volltext

Verfügbarkeit prüfen

Eicosanoids and Their Drugs in Cardiovascular Diseases: Focus on Atherosclerosis and Stroke

Medicinal research reviews, 2013-03, Vol.33 (2), p.364-438

2013

Link zum Volltext

Verfügbarkeit prüfen

Antagonism of thromboxane receptors by diclofenac and lumiracoxib

British journal of pharmacology, 2007-12, Vol.152 (8), p.1185-1195

2007

Link zum Volltext

Verfügbarkeit prüfen

Thromboxane prostanoid receptor in human airway smooth muscle cells: a relevant role in proliferation

European journal of pharmacology, 2003-08, Vol.474 (2), p.149-159

2003

Link zum Volltext

Verfügbarkeit prüfen

Brain damage as detected by cDNA-microarray in the spinal fluid of patients with Aicardi-Goutieres syndrome

Neurology, 2008-08, Vol.71 (8), p.610

2008

Link zum Volltext

Verfügbarkeit prüfen

Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma

Neuropathology and applied neurobiology, 2008-06, Vol.34 (3), p.306-315

2008

Link zum Volltext

Verfügbarkeit prüfen

Leukotrienes and atherosclerosis

Current drug targets, 2010-07, Vol.11 (7), p.882

2010

Link zum Volltext

Verfügbarkeit prüfen

Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

Human molecular genetics, 2011-11, Vol.20 (22), p.4324-4333

2011

Link zum Volltext

Verfügbarkeit prüfen

Antagonism of thromboxane receptors by diclofenac and lumiracoxib

British journal of pharmacology, 2008-04, Vol.153 (8), p.1763-1763

2008

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly

Toward understanding the genetic basis of neural tube defects

Contribution of VANGL2 mutations to isolated neural tube defects

Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy

The DRY motif at work: the P2Y12 receptor case

Structural Connectivity Analysis in Children with Segmental Callosal Agenesis

In vitro pharmacological evaluation of multitarget thromboxane prostanoid receptor/COX-2 agents: A possible strategy to solve the cardiovascular issues of COXIBs

Expanding the mutational spectrum associated to neural tube defects: Literature revision and description of novel VANGL1 mutations

Cysteinyl-leukotriene receptor antagonists: present situation and future opportunities

Beyond spinal muscular atrophy with lower extremity dominance: cerebellar hypoplasia associated with a novel mutation in BICD2

Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations

Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly

Molecular and functional aspects of human cysteinyl leukotriene receptors

Leukotrienes as Mediators of Asthma

Montelukast and cardiovascular risk in asthmatics

Eicosanoids and Their Drugs in Cardiovascular Diseases: Focus on Atherosclerosis and Stroke

Antagonism of thromboxane receptors by diclofenac and lumiracoxib

Thromboxane prostanoid receptor in human airway smooth muscle cells: a relevant role in proliferation

Brain damage as detected by cDNA-microarray in the spinal fluid of patients with Aicardi-Goutieres syndrome

Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma

Leukotrienes and atherosclerosis

Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans

Antagonism of thromboxane receptors by diclofenac and lumiracoxib

Suchergebnisse filtern