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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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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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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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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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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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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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New Function for NF1 Tumor Suppressor

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

2000

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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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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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O.06a Nocturnal variability of coagulation in gestational diabetes

Thrombosis research, 2011, Vol.127, p.S125-S126

2011

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POLSSS: surveying stakeholders about acceptability of risks and system changes

Safety science, 2000-06, Vol.35 (1), p.123-137

Poeyhoenen, M

2000

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008 Congenital anomalies in neurofibromatosis 1: A retrospective register-based total population study

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S194-S194

2017

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Detection of the founder effect in Finnish CADASIL families

European journal of human genetics : EJHG, 2004-10, Vol.12 (10), p.813-819

2004

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Risk of malignancy and death in neurofibromatosis

Archives of pathology & laboratory medicine (1976), 1997-02, Vol.121 (2), p.139

1997

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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

Neurogenetics, 2006-07, Vol.7 (3), p.185-194

2006

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P-025 Adrenomedullin is associated with von Willebrand factor activity in non-pregnant but not in pregnant women

Thrombosis research, 2013, Vol.131, p.S83-S83

2013

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Extensive somatic microsatellite mutations in normal human tissue

Cancer research (Chicago, Ill.), 2001-06, Vol.61 (11), p.4541-4544

2001

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Accelerated splanchnic amino acid uptake after cardiac surgery

Clinical nutrition (Edinburgh, Scotland), 1998-04, Vol.17 (2), p.51-55

1998

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Effects of sympatholytic therapy on postmenopausal symptoms in hypertensive postmenopausal women

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

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

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

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

New Function for NF1 Tumor Suppressor

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

Behavioral and procedural consequences of structural variation in value trees

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

O.06a Nocturnal variability of coagulation in gestational diabetes

POLSSS: surveying stakeholders about acceptability of risks and system changes

008 Congenital anomalies in neurofibromatosis 1: A retrospective register-based total population study

Detection of the founder effect in Finnish CADASIL families

Risk of malignancy and death in neurofibromatosis

Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

P-025 Adrenomedullin is associated with von Willebrand factor activity in non-pregnant but not in pregnant women

Extensive somatic microsatellite mutations in normal human tissue

Accelerated splanchnic amino acid uptake after cardiac surgery

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