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Items: 20

1.

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

van der Kooi AJ, Frankhuizen WS, Barth PG, Howeler CJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, van Ommen GJ, de Visser M, Bakker E, Ginjaar HB.

Neurology. 2007 Jun 12;68(24):2125-8.

PMID:
17562833
2.

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

Badrising UA, Maat-Schieman ML, Ferrari MD, Zwinderman AH, Wessels JA, Breedveld FC, van Doorn PA, van Engelen BG, Hoogendijk JE, Höweler CJ, de Jager AE, Jennekens FG, Koehler PJ, de Visser M, Viddeleer A, Verschuuren JJ, Wintzen AR.

Ann Neurol. 2002 Mar;51(3):369-72.

PMID:
11891832
3.

Age and causes of death in adult-onset myotonic dystrophy.

de Die-Smulders CE, Höweler CJ, Thijs C, Mirandolle JF, Anten HB, Smeets HJ, Chandler KE, Geraedts JP.

Brain. 1998 Aug;121 ( Pt 8):1557-63.

PMID:
9712016
4.

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

Linssen WH, Notermans NC, Van der Graaf Y, Wokke JH, Van Doorn PA, Höweler CJ, Busch HF, De Jager AE, De Visser M.

Brain. 1997 Nov;120 ( Pt 11):1989-96.

PMID:
9397016
5.

Paternal transmission of congenital myotonic dystrophy.

de Die-Smulders CE, Smeets HJ, Loots W, Anten HB, Mirandolle JF, Geraedts JP, Höweler CJ.

J Med Genet. 1997 Nov;34(11):930-3.

6.

Vocational perspectives and neuromuscular disorders.

Andries F, Wevers CW, Wintzen AR, Busch HF, Höweler CJ, de Jager AE, Padberg GW, de Visser M, Wokke JH.

Int J Rehabil Res. 1997 Sep;20(3):255-73.

PMID:
9331576
7.

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

van der Kooi AJ, Barth PG, Busch HF, de Haan R, Ginjaar HB, van Essen AJ, van Hooff LJ, Höweler CJ, Jennekens FG, Jongen P, Oosterhuis HJ, Padberg GW, Spaans F, Wintzen AR, Wokke JH, Bakker E, van Ommen GJ, Bolhuis PA, de Visser M.

Brain. 1996 Oct;119 ( Pt 5):1471-80.

PMID:
8931572
8.

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

Schrander-Stumpel CT, Höweler CJ, Fryns JP.

Genet Couns. 1995;6(1):21-32. Review.

PMID:
7794558
9.

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

de Die-Smulders CE, Höweler CJ, Mirandolle JF, Brunner HG, Hovers V, Brüggenwirth H, Smeets HJ, Geraedts JP.

J Med Genet. 1994 Aug;31(8):595-601.

10.

[An unstable mutation as cause of myotonic dystrophy].

Brunner HG, Höweler CJ, Smeets HJ, Wieringa B.

Ned Tijdschr Geneeskd. 1993 Nov 27;137(48):2468-72. Review. Dutch. No abstract available.

PMID:
8272119
11.

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

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al.

Am J Hum Genet. 1993 Nov;53(5):1016-23.

12.

Brief report: reverse mutation in myotonic dystrophy.

Brunner HG, Jansen G, Nillesen W, Nelen MR, de Die CE, Höweler CJ, van Oost BA, Wieringa B, Ropers HH, Smeets HJ.

N Engl J Med. 1993 Feb 18;328(7):476-80. No abstract available.

13.

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

Schrander-Stumpel CT, Höweler CJ, Reekers AD, De Smet NM, Hall JG, Fryns JP.

J Med Genet. 1993 Jan;30(1):78-80. Review.

14.

Intestinal pseudo-obstruction in myotonic dystrophy.

Brunner HG, Hamel BC, Rieu P, Höweler CJ, Peters FT.

J Med Genet. 1992 Nov;29(11):791-3.

15.

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

Schrander-Stumpel C, Fryns J, Cassiman JJ, Legius E, Spaepen A, Höweler CJ.

J Med Genet. 1992 Mar;29(3):215. No abstract available.

16.

Anticipation in myotonic dystrophy: fact or fiction?

Höweler CJ, Busch HF, Geraedts JP, Niermeijer MF, Staal A.

Brain. 1989 Jun;112 ( Pt 3):779-97.

PMID:
2731029
17.

[Current viewpoints in dystrophia myotonica].

Höweler CJ.

Ned Tijdschr Geneeskd. 1988 Jun 4;132(23):1076-8. Dutch. No abstract available.

PMID:
3386769
18.

Two Dutch siblings with congenital muscular dystrophy (Fukuyama type).

Vles JS, de Krom MC, Visser R, Höweler CJ.

Clin Neurol Neurosurg. 1983;85(3):175-80.

PMID:
6315292
19.

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

Höweler CJ, Busch HF, Bernini LF, van Loghem E, Meera Khan P, Nijenhuis LE.

Brain. 1980 Sep;103(3):497-513.

PMID:
7417778
20.

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