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Items: 1 to 20 of 398

1.

Type IV Ehlers-Danlos syndrome with aspirin sensitivity. A family study.

Grenko RT, Burns SL, Golden EA, Byers PH, Bovill EG.

Arch Pathol Lab Med. 1993 Oct;117(10):989-92.

PMID:
8215841
2.

Platelet and coagulation studies in Ehlers-Danlos syndrome.

Anstey A, Mayne K, Winter M, Van de Pette J, Pope FM.

Br J Dermatol. 1991 Aug;125(2):155-63.

PMID:
1911298
3.
4.

Collagen and bleeding diathesis in Ehlers-Danlos syndrome.

Udén A.

Scand J Haematol. 1982 May;28(5):425-30.

PMID:
7123147
5.

Ehlers-Danlos syndrome IV due to a novel defect in type III procollagen.

Pyeritz RE, Stolle CA, Parfrey NA, Myers JC.

Am J Med Genet. 1984 Nov;19(3):607-22.

PMID:
6507506
6.

Ehlers-Danlos syndrome type IV mimicking non-accidental injury in a child.

Roberts DL, Pope FM, Nicholls AC, Narcisi P.

Br J Dermatol. 1984 Sep;111(3):341-5.

PMID:
6477831
7.

Arterial rupture in classic Ehlers-Danlos syndrome with COL5A1 mutation.

Borck G, Beighton P, Wilhelm C, Kohlhase J, Kubisch C.

Am J Med Genet A. 2010 Aug;152A(8):2090-3. doi: 10.1002/ajmg.a.33541.

PMID:
20635400
10.

Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism.

Palmeri S, Mari F, Meloni I, Malandrini A, Ariani F, Villanova M, Pompilio A, Schwarze U, Byers PH, Renieri A.

Clin Genet. 2003 Jun;63(6):510-5.

PMID:
12786757
11.

Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII.

Hartsfield JK Jr, Kousseff BG.

Am J Med Genet. 1990 Dec;37(4):465-70. Review.

PMID:
2260589
12.

Ehlers-Danlos syndrome and type III collagen abnormalities: a variable clinical spectrum.

Hamel BC, Pals G, Engels CH, van den Akker E, Boers GH, van Dongen PW, Steijlen PM.

Clin Genet. 1998 Jun;53(6):440-6.

PMID:
9712532
13.

Familial spastic ataxia associated with Ehlers-Danlos syndrome with platelet dysfunction.

Chouza C, Caamaño JL, De Medina O, Bogacz J, Oehninger C, Vignale R, De Anda G, Novoa E, De Bellis R, Cardozo H, et al.

Can J Neurol Sci. 1984 Nov;11(4 Suppl):541-9.

PMID:
6509400
14.

[Ehlers-Danlos syndrome IV: phenotype variation].

Engels CH, van Dongen PW, Boers GH, Steijlen PM, Hamel BC.

Ned Tijdschr Geneeskd. 1997 Feb 8;141(6):296-8. Dutch.

PMID:
9148166
15.

Death due to Ehlers-Danlos syndrome type IV.

Prahlow JA, Wagner SA.

Am J Forensic Med Pathol. 2005 Mar;26(1):78-82.

PMID:
15725781
16.

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.

Br J Dermatol. 1987 Jul;117(1):89-97.

PMID:
3651336
18.

Alpha2-macroglobulin deficiency in a patient with Ehlers-Danlos syndrome.

Mahour GH, Song MK, Adham NF, Rinderknecht H.

Pediatrics. 1978 Jun;61(6):894-7.

PMID:
79166
20.

Hereditary epidermolytic palmoplantar keratoderma (Vörner type) in a family with Ehlers-Danlos syndrome.

Mofid MZ, Costarangos C, Gruber SB, Koch SE.

J Am Acad Dermatol. 1998 May;38(5 Pt 2):825-30.

PMID:
9591795

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