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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

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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

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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

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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

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

Neurology, 2002-09, Vol.59 (5), p.759-761

2002

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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

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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

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

Neurology, 2003-11, Vol.61 (10), p.1397-1400

2003

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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

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Loss of SUFU Function in Familial Multiple Meningioma

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

2012

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Molecular genetic and clinical findings in identical twins with CADASIL

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

2009

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Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation

Stroke (1970), 2001-08, Vol.32 (8), p.1767-1774

2001

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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

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

2019

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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

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

2009

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Genetic factors modify the clinical course of CADASIL

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

2009

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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

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Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

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

1998

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On the convergence of multiattribute weighting methods

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

2001

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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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Independent NF1 mutations in two large families with spinal neurofibromatosis

Journal of medical genetics, 2003-02, Vol.40 (2), p.122-126

2003

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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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Hereditary spinal neurofibromatosis: a rare form of NF1?

Journal of medical genetics, 1997-03, Vol.34 (3), p.184-187

1997

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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

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

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

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

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

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation

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

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

Independent NF1 mutations in two large families with spinal neurofibromatosis

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

Hereditary spinal neurofibromatosis: a rare form of NF1?

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