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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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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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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

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CADASIL and CARASIL

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

2014

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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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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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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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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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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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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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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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Insulin resistance and sympathetic overactivity in women

Journal of hypertension, 2006-01, Vol.24 (1), p.131-141

2006

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Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description

Annals of neurology, 1994-09, Vol.36 (3), p.362-367

1994

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Increased urinary polyamine excretion after starting a very low calorie diet

Scandinavian journal of clinical and laboratory investigation, 1993, Vol.53 (8), p.811-819

1993

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Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1

American journal of medical genetics, 2000-11, Vol.95 (2), p.108-117

2000

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Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy

Human molecular genetics, 2013-08, Vol.22 (15), p.2975-2983

2013

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Identification of SPRED1 deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR

American journal of medical genetics. Part A, 2011-06, Vol.155 (6), p.1352-1359

2011

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Effects of aquatic resistance training on neuromuscular performance in healthy women

Medicine and science in sports and exercise, 2002-12, Vol.34 (12), p.2103-2109

2002

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Adrenal Pheochromocytoma—Ganglioneuroma Producing Catecholamines and Various Neuropeptides

Acta Medica Scandinavica, 1988-01, Vol.224 (4), p.403-408

1988

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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

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

CADASIL and CARASIL

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

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

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

Arterioles of the lenticular nucleus in CADASIL

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

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

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

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

Detection of the founder effect in Finnish CADASIL families

Insulin resistance and sympathetic overactivity in women

Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description

Increased urinary polyamine excretion after starting a very low calorie diet

Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1

Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy

Identification of SPRED1 deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR

Effects of aquatic resistance training on neuromuscular performance in healthy women

Adrenal Pheochromocytoma—Ganglioneuroma Producing Catecholamines and Various Neuropeptides

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