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Fragile-X syndrome - a 20-year follow-up study of male patients

Clinical genetics, 2016-01, Vol.89 (1), p.55-59

Arvio, M.

2016

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Medicine use in people with intellectual disabilities: a Finnish nationwide register study

Journal of intellectual disability research, 2023-12, Vol.67 (12), p.1291-1305

2023

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Down syndrome in adults: a 27-year follow-up of adaptive skills

Clinical genetics, 2016-11, Vol.90 (5), p.456-460

2016

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Prevalence, aetiology and comorbidity of severe and profound intellectual disability in Finland

Journal of intellectual disability research, 2003-02, Vol.47 (2), p.108-112

2003

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Cardiovascular manifestations in 75 patients with Williams syndrome

Journal of medical genetics, 2002-08, Vol.39 (8), p.554-558

2002

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Need for special units for the management of neuropsychiatric disorders in people with intellectual disabilities

Acta psychiatrica Scandinavica, 2014-08, Vol.130 (2), p.77-79

2014

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Fragile-X syndromeￂ -ￂ a 20-year follow-up study of male patients

Clinical genetics, 2016-01, Vol.89 (1), p.55

Arvio, M

2016

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Consensus guidelines into the management of epilepsy in adults with an intellectual disability

Journal of intellectual disability research, 2009-08, Vol.53 (8), p.687-694

2009

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Vitamin D status and optimal supplementation in institutionalized adults with intellectual disability

Journal of intellectual disability research, 2009-12, Vol.53 (12), p.1014-1023

2009

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Topiramate in long-term treatment of epilepsy in the intellectually disabled

Journal of intellectual disability research, 2005-03, Vol.49 (3), p.183-189

2005

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Cardiolipin and β2 -Glycoprotein I antibodies associate with cognitive impairment and seizure frequency in developmental disorders

Seizure (London, England), 2011-07, Vol.20 (6), p.438-441

2011

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Vitamin D status and optimal supplementation in institutionalized adults with intellectual disability

BONE, 2009, Vol.45, p.S88-S89

2009

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Reduction in head size in patients with aspartylglucosaminuria

Acta neurologica Scandinavica, 2005-11, Vol.112 (5), p.335-337

2005

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Follow-up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions

Acta Paediatrica, 1993-05, Vol.82 (5), p.469-471

Arvio, M

1993

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Follow-up in patients with aspartylglucosaminuria. Part II. Adaptive skills

Acta Paediatrica, 1993-06, Vol.82 (6-7), p.590-594

Arvio, M

1993

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Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria

Journal of medical genetics, 1999-05, Vol.36 (5), p.398-404

1999

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Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritis

Annals of the rheumatic diseases, 2002-02, Vol.61 (2), p.180-181

2002

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Chronic arthritis in patients with aspartylglucosaminuria

Journal of rheumatology, 1998-06, Vol.25 (6), p.1131

1998

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Applicability of a checklist for clinical screening of the fragile X syndrome

Clinical genetics, 1997-10, Vol.52 (4), p.211-215

1997

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A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria

Clinical genetics, 2000-12, Vol.58 (6), p.447-454

2000

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Early clinical symptoms and incidence of aspartylglucosaminuria in Finland

Acta Paediatrica, 1993-06, Vol.82 (6-7), p.587-589

1993

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Prevalence, aetiology, and comorbidity of severe and profound intellectual disability (SPID) in Finland

Journal of intellectual disability research, 2004-06, Vol.48, p.429

2004

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Progressive nature of aspartylglucosaminuria

Acta Paediatrica, 2002-03, Vol.91 (3), p.255-257

2002

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Cardiolipin and β 2-Glycoprotein I antibodies associate with cognitive impairment and seizure frequency in developmental disorders

Seizure (London, England), 2011, Vol.20 (6), p.438-441

2011

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Bone mineral density and sex hormone status in intellectually disabled women on progestin-induced amenorrhea

Acta obstetricia et gynecologica Scandinavica, 2009-01, Vol.88 (4), p.428-433

2009

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Fragile-X syndrome - a 20-year follow-up study of male patients

Medicine use in people with intellectual disabilities: a Finnish nationwide register study

Down syndrome in adults: a 27-year follow-up of adaptive skills

Prevalence, aetiology and comorbidity of severe and profound intellectual disability in Finland

Cardiovascular manifestations in 75 patients with Williams syndrome

Need for special units for the management of neuropsychiatric disorders in people with intellectual disabilities

Fragile-X syndromeￂ -ￂ a 20-year follow-up study of male patients

Consensus guidelines into the management of epilepsy in adults with an intellectual disability

Vitamin D status and optimal supplementation in institutionalized adults with intellectual disability

Topiramate in long-term treatment of epilepsy in the intellectually disabled

Cardiolipin and β2 -Glycoprotein I antibodies associate with cognitive impairment and seizure frequency in developmental disorders

Vitamin D status and optimal supplementation in institutionalized adults with intellectual disability

Reduction in head size in patients with aspartylglucosaminuria

Follow-up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions

Follow-up in patients with aspartylglucosaminuria. Part II. Adaptive skills

Overgrowth of oral mucosa and facial skin, a novel feature of aspartylglucosaminuria

Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritis

Chronic arthritis in patients with aspartylglucosaminuria

Applicability of a checklist for clinical screening of the fragile X syndrome

A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria

Early clinical symptoms and incidence of aspartylglucosaminuria in Finland

Prevalence, aetiology, and comorbidity of severe and profound intellectual disability (SPID) in Finland

Progressive nature of aspartylglucosaminuria

Cardiolipin and β 2-Glycoprotein I antibodies associate with cognitive impairment and seizure frequency in developmental disorders

Bone mineral density and sex hormone status in intellectually disabled women on progestin-induced amenorrhea

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