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Items: 1 to 20 of 131

1.

Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects.

Leoni A, Cetta G, Tenni R, Pasquali-Ronchetti I, Bertolini F, Guerra D, Dyne K, Castellani A.

Arch Dermatol. 1987 Apr;123(4):493-9.

PMID:
3827281
2.

Chronic leg ulcerations resembling vasculitis in two siblings with prolidase deficiency.

Cantatore FP, Papadia F, Giannico G, Simonetti S, Carrozzo M.

Clin Rheumatol. 1993 Sep;12(3):410-4.

PMID:
8258246
3.

[Hereditary prolidase deficiency in 2 sisters with therapy-resistant leg ulcers].

Voigtländer V, Fischer E, Larrègue M.

Hautarzt. 1988 Apr;39(4):247-9. German.

PMID:
3384668
4.

Ulcus cruris associated with prolidase deficiency.

Kavala M, Zindanci I, Sudogan S, Turkoglu Z, Sarigul S.

Dermatol Online J. 2006 Dec 10;12(7):24.

PMID:
17459310
5.

[Hereditary prolidase deficiency. Contribution to differential therapy refractory leg ulcer diagnosis].

Kasten R, Steinmann B, Voigtländer V.

Hautarzt. 2000 Nov;51(11):846-51. German.

PMID:
11116849
6.

Prolidase deficiency: its dermatological manifestations and some additional biochemical studies.

Arata J, Umemura S, Yamamoto Y, Hagiyama M, Nohara N.

Arch Dermatol. 1979 Jan;115(1):62-7.

PMID:
760660
7.

Autosomal recessive prolidase deficiency. Three patients with recalcitrant ulcers.

Ogata A, Tanaka S, Tomoda T, Murayama E, Endo F, Kikuchi I.

Arch Dermatol. 1981 Nov;117(11):689-97.

PMID:
7316526
8.

Ultrastructural studies on dermis from prolidase deficient subjects.

Pasquali Ronchetti I, Quaglino D Jr, Dyne KM, Zanaboni G, Cetta G.

J Submicrosc Cytol Pathol. 1991 Jul;23(3):439-45.

PMID:
1913589
9.

Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients.

Zanaboni G, Dyne KM, Rossi A, Monafo V, Cetta G.

Haematologica. 1994 Jan-Feb;79(1):13-8.

10.

Prolidase deficiency: a multisystemic hereditary disorder.

Bissonnette R, Friedmann D, Giroux JM, Dolenga M, Hechtman P, Der Kaloustian VM, Dubuc R.

J Am Acad Dermatol. 1993 Nov;29(5 Pt 2):818-21.

PMID:
8408817
11.

Clinical and biochemical characteristics of prolidase deficiency in siblings.

Freij BJ, Levy HL, Dudin G, Mutasim D, Deeb M, Der Kaloustian VM.

Am J Med Genet. 1984 Nov;19(3):561-71.

PMID:
6507502
12.

Pathogenesis of ulcerations in deficiency of prolidase. The role of angiopathy and of deposits of amyloid.

Pierard GE, Cornil F, Lapiere CM.

Am J Dermatopathol. 1984 Oct;6(5):491-7.

PMID:
6507815
13.

[Prolidase and manganese deficiency. Apropos of a case: diagnosis and treatment].

Larrèque M, Charpentier C, Laidet B, Lambert M, Bressieux JM, Prigent F, Canuel C, Tanzer J.

Ann Dermatol Venereol. 1982;109(8):667-78. French.

PMID:
7187192
14.
15.

Prolidase deficiency with imidodipeptiduria. A familial case with and without clinical symptoms.

Isemura M, Hanyu T, Gejyo F, Nakazawa R, Igarashi R, Matsuo S, Ikeda K, Sato Y.

Clin Chim Acta. 1979 May 2;93(3):401-7.

PMID:
445856
16.

Prolidase deficiency with iminodipeptiduria: biochemical investigations and first results of attempted therapy.

Charpentier C, Dagbovie K, Lemonnier A, Larregue M, Johnstone RA.

J Inherit Metab Dis. 1981;4(2):77-8.

PMID:
6790856
17.

A case of prolidase deficiency accompanying leg ulcers.

Solak B, Kara RO, Erdem T, Muftuoglu T.

Int J Low Extrem Wounds. 2015 Mar;14(1):92-4. doi: 10.1177/1534734615570360. Epub 2015 Feb 17.

PMID:
25691319
18.

Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes.

Jackson SH, Dennis AW, Greenberg M.

Can Med Assoc J. 1975 Oct 18;113(8):759, 762-3.

19.

Prolidase deficiency: a patient without hydroxyproline-containing iminodipeptides in urine.

Wysocki SJ, Hahnel R, Mahoney T, Wilson RG, Panegyres PK.

J Inherit Metab Dis. 1988;11(2):161-5.

PMID:
3139928
20.

Studies on prolidase deficiency with a possible defect in collagen metabolism.

Isemura M, Hanyu T, Ono T, Igarashi R, Sato Y, Gejyo F, Nakazawa R, Miyakawa T, Takagi T, Kuboki Y, Sasaki S.

Tohoku J Exp Med. 1981 May;134(1):21-8.

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