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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

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Experimental studies of mitochondrial function in CADASIL vascular smooth muscle cells

Experimental cell research, 2013-02, Vol.319 (3), p.134-143

2013

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Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.e29-e29

2017

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0710: Surveillance of Women at High Risk of Gynecological Cancers: 10 Year Results From One Center

International journal of gynecological cancer, 2006-10, Vol.16 (Suppl 3), p.799-799

2006

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Imbalance of the autonomic nervous system at night in women with gestational diabetes

Diabetic medicine, 2010-09, Vol.27 (9), p.988-994

2010

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CADASIL: hereditary disease of arteries causing brain infarcts and dementia

Neuropathology and applied neurobiology, 1999-08, Vol.25 (4), p.257-265

1999

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Congenital pseudarthrosis of the tibia: Treatment and outcome at skeletal maturity in 10 children

Acta orthopaedica, 1999, Vol.70 (3), p.275-282

1999

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CADASIL Mutations and shRNA Silencing of NOTCH3 Affect Actin Organization in Cultured Vascular Smooth Muscle Cells

Journal of cerebral blood flow and metabolism, 2012-12, Vol.32 (12), p.2171-2180

2012

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Arterioles of the lenticular nucleus in CADASIL

Stroke (1970), 2006-09, Vol.37 (9), p.2242-2247

2006

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Neurologic symptoms are common during gestation and puerperium in CADASIL

Neurology, 2005-04, Vol.64 (8), p.1441-1443

2005

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Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Brain pathology (Zurich, Switzerland), 2004-10, Vol.14 (4), p.358-364

2004

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Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation

Stroke (1970), 2009-06, Vol.40 (6), p.2215-2218

2009

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Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease

Nature medicine, 2000-03, Vol.6 (3), p.343-345

2000

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Insidious cognitive decline in CADASIL

Stroke (1970), 2004-07, Vol.35 (7), p.1598-1602

2004

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Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

Journal of clinical oncology, 2005-07, Vol.23 (21), p.4609-4616

2005

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New Function for NF1 Tumor Suppressor

Journal of investigative dermatology, 2000-03, Vol.114 (3), p.473-479

2000

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Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients

Stroke (1970), 2004-05, Vol.35 (5), p.1063-1067

2004

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Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions

Genetics in medicine, 2007-10, Vol.9 (10), p.690-694

2007

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Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy : A cross-sectional study

Ophthalmology (Rochester, Minn.), 2006-08, Vol.113 (8), p.1411-1417

2006

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Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patient

Molecular medicine (Cambridge, Mass.), 2007-05, Vol.13 (5-6), p.305-314

2007

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Auditory-evoked potentials in bispectral index-guided anaesthesia for cardiac surgery

European journal of anaesthesiology, 2007-07, Vol.24 (7), p.571-579

2007

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Behavioral and procedural consequences of structural variation in value trees

European journal of operational research, 2001-10, Vol.134 (1), p.216-227

2001

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The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients

Acta dermato-venereologica, 2017-04, Vol.97 (4), p.456-463

2017

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Scanning Laser Doppler Flowmetry Shows Reduced Retinal Capillary Blood Flow in CADASIL

Stroke (1970), 2004-11, Vol.35 (11), p.2449-2452

2004

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

Experimental studies of mitochondrial function in CADASIL vascular smooth muscle cells

Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1

0710: Surveillance of Women at High Risk of Gynecological Cancers: 10 Year Results From One Center

Imbalance of the autonomic nervous system at night in women with gestational diabetes

CADASIL: hereditary disease of arteries causing brain infarcts and dementia

Congenital pseudarthrosis of the tibia: Treatment and outcome at skeletal maturity in 10 children

CADASIL Mutations and shRNA Silencing of NOTCH3 Affect Actin Organization in Cultured Vascular Smooth Muscle Cells

Arterioles of the lenticular nucleus in CADASIL

Neurologic symptoms are common during gestation and puerperium in CADASIL

Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation

Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease

Insidious cognitive decline in CADASIL

Molecular Analysis of Familial Endometrial Carcinoma: A Manifestation of Hereditary Nonpolyposis Colorectal Cancer or a Separate Syndrome?

New Function for NF1 Tumor Suppressor

Positron emission tomography examination of cerebral blood flow and glucose metabolism in young CADASIL patients

Molecular analysis of the CHD7 gene in CHARGE syndrome: identification of 22 novel mutations and evidence for a low contribution of large CHD7 deletions

Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy : A cross-sectional study

Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patient

Auditory-evoked potentials in bispectral index-guided anaesthesia for cardiac surgery

Behavioral and procedural consequences of structural variation in value trees

The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients

The structure of the presenilin 1 ( S182 ) gene and identification of six novel mutations in early onset AD families

Scanning Laser Doppler Flowmetry Shows Reduced Retinal Capillary Blood Flow in CADASIL

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