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Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Neurology, 2000-11, Vol.55 (9), p.1385

2000

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Age and causes of death in adult-onset myotonic dystrophy

Brain (London, England : 1878), 1998-08, Vol.121 (8), p.1557-1563

1998

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Miyoshi-type distal muscular dystrophy : Clinical spectrum in 24 Dutch patients

Brain (London, England : 1878), 1997-11, Vol.120 (11), p.1989-1996

1997

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The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands

Brain (London, England : 1878), 1996-10, Vol.119 (5), p.1471-1480

1996

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Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Neurology, 2007-06, Vol.68 (24), p.2125

2007

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Paternal transmission of congenital myotonic dystrophy

Journal of medical genetics, 1997-11, Vol.34 (11), p.930-933

1997

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Intestinal pseudo-obstruction in myotonic dystrophy

Journal of medical genetics, 1992-11, Vol.29 (11), p.791-793

1992

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ANTICIPATION IN MYOTONIC DYSTROPHY: FACT OR FICTION?

Brain (London, England : 1878), 1989-06, Vol.112 (3), p.779-797

1989

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Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)

American journal of human genetics, 1993-11, Vol.53 (5), p.1016-1023

1993

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Vocational perspectives and neuromuscular disorders

International journal of rehabilitation research, 1997-09, Vol.20 (3), p.255-274

1997

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Gonosomal mosaicism in myotonic dystrophy patients : involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm

American journal of human genetics, 1994-04, Vol.54 (4), p.575-585

1994

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X-linked mental retardation and neurological symptoms: a nosological approach

Genetic counseling, 1995, Vol.6 (1), p.21

1995

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Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis

Journal of medical genetics, 1993-01, Vol.30 (1), p.78-80

1993

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Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family

Journal of medical genetics, 1994-08, Vol.31 (8), p.595-601

1994

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Brief report : reverse mutation in myotonic dystrophy

The New England journal of medicine, 1993-02, Vol.328 (7), p.476-480

1993

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Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo

Annals of neurology, 2002-03, Vol.51 (3), p.369-372

2002

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Two dutch siblings with congenital muscular dystrophy (Fukuyama type)

Clinical neurology and neurosurgery, 1983, Vol.85 (3), p.175-180

1983

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Gonosomal mosaicism in myotonic dystrophy patients: Involvement of mitotic events in (CTG)[sub n] repeat variation and selection against extreme expansion in sperm

American journal of human genetics, 1994-04, Vol.54:4

1994

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MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families

Journal of medical genetics, 1992-03, Vol.29 (3), p.215-215

1992

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Current viewpoints in dystrophia myotonica

Nederlands tijdschrift voor geneeskunde, 1988-06, Vol.132 (23), p.1076

Höweler, C J

1988

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Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports

Archives of disease in childhood, 1979-05, Vol.54 (5), p.331-338

1979

Volltextzugriff (PDF)

Influence of sex of the transmitting parent as well as of parental allele site on the CTG expansion in myotonic dystrophy (DM)

American journal of human genetics, 1993-11, Vol.53 (5), p.1016-1023

1993

Volltextzugriff (PDF)

An unstable mutation as cause of myotonic dystrophy

Nederlands tijdschrift voor geneeskunde, 1993-11, Vol.137 (48), p.2468

1993

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Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families

American journal of medical genetics, 1995-05, Vol.57 (1), p.107-116

1995

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Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study

Brain (London, England : 1878), 1980-09, Vol.103 (3), p.497-513

1980

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Epidemiology of inclusion body myositis in the Netherlands: a nationwide study

Age and causes of death in adult-onset myotonic dystrophy

Miyoshi-type distal muscular dystrophy : Clinical spectrum in 24 Dutch patients

The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands

Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Paternal transmission of congenital myotonic dystrophy

Intestinal pseudo-obstruction in myotonic dystrophy

ANTICIPATION IN MYOTONIC DYSTROPHY: FACT OR FICTION?

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)

Vocational perspectives and neuromuscular disorders

Gonosomal mosaicism in myotonic dystrophy patients : involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm

X-linked mental retardation and neurological symptoms: a nosological approach

Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis

Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family

Brief report : reverse mutation in myotonic dystrophy

Comparison of weakness progression in inclusion body myositis during treatment with methotrexate or placebo

Two dutch siblings with congenital muscular dystrophy (Fukuyama type)

Gonosomal mosaicism in myotonic dystrophy patients: Involvement of mitotic events in (CTG)[sub n] repeat variation and selection against extreme expansion in sperm

MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families

Current viewpoints in dystrophia myotonica

Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports

Influence of sex of the transmitting parent as well as of parental allele site on the CTG expansion in myotonic dystrophy (DM)

An unstable mutation as cause of myotonic dystrophy

Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families

Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study

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