Matton M - Search Results

1

Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type III.

De Paepe A, Nicholls A, Narcisi P, De Keyser F, Quatacker J, Van Staey M, Matton M, Pope FM. De Paepe A, et al. Among authors: matton m. Br J Dermatol. 1987 Jul;117(1):89-97. doi: 10.1111/j.1365-2133.1987.tb04096.x. Br J Dermatol. 1987. PMID: 3651336

2

Obstetrical problems in patients with Ehlers-Danlos syndrome type IV; a case report.

De Paepe A, Thaler B, Van Gijsegem M, Van Hoecke D, Matton M. De Paepe A, et al. Among authors: matton m. Eur J Obstet Gynecol Reprod Biol. 1989 Nov;33(2):189-93. doi: 10.1016/0028-2243(89)90214-1. Eur J Obstet Gynecol Reprod Biol. 1989. PMID: 2583342

3

Linkage of a polymorphic marker for the type III collagen gene (COL3A1) to atypical autosomal dominant Ehlers-Danlos syndrome type IV in a large Belgian pedigree.

Nicholls AC, De Paepe A, Narcisi P, Dalgleish R, De Keyser F, Matton M, Pope FM. Nicholls AC, et al. Among authors: matton m. Hum Genet. 1988 Mar;78(3):276-81. doi: 10.1007/BF00291676. Hum Genet. 1988. PMID: 3162228

4

[The Ehlers-Danlos and Marfan syndromes in young children].

De Paepe A, Van den Bossche H, Mortier G, Matton M. De Paepe A, et al. Among authors: matton m. J Genet Hum. 1988 Jun;36(3):247-53. J Genet Hum. 1988. PMID: 3411305 French.

5

Pulse wave velocity recordings in a family with ecchymotic Ehlers-Danlos syndrome.

François B, De Paepe A, Matton MT, Clement D. François B, et al. Among authors: matton mt. Int Angiol. 1986 Jan-Mar;5(1):1-5. Int Angiol. 1986. PMID: 3734513

6

Unusual familial manifestation of Ehlers-Danlos syndrome.

Matton MT, De Paepe A, De Keyser F, François B. Matton MT, et al. Prog Clin Biol Res. 1982;104:243-58. Prog Clin Biol Res. 1982. PMID: 7163270

7

Trisomy 3 mosaicism in a patient with Bartter syndrome.

De Keyser F, Matthys E, De Paepe A, Verschraegen-Spae MR, Matton M. De Keyser F, et al. Among authors: matton m. J Med Genet. 1988 May;25(5):358. doi: 10.1136/jmg.25.5.358. J Med Genet. 1988. PMID: 3385747 Free PMC article. No abstract available.

8

Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner families.

De Paepe A, Viljoen D, Matton M, Beighton P, Lenaerts V, Vossaert K, De Bie S, Voet D, De Laey JJ, Kint A. De Paepe A, et al. Among authors: matton m. Am J Med Genet. 1991 Jan;38(1):16-20. doi: 10.1002/ajmg.1320380105. Am J Med Genet. 1991. PMID: 2012127

9

Turner's syndrome: updating on diagnosis and therapy.

De Paepe A, Matton M. De Paepe A, et al. Among authors: matton m. Prog Clin Biol Res. 1985;200:283-300. Prog Clin Biol Res. 1985. PMID: 3841212 No abstract available.

10

Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO).

Meire F, De Laey JJ, de Bie S, van Staey M, Matton MT. Meire F, et al. Among authors: matton mt. Ophthalmic Paediatr Genet. 1985 Feb;5(1-2):91-7. doi: 10.3109/13816818509007861. Ophthalmic Paediatr Genet. 1985. PMID: 4058877

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