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Items: 1 to 20 of 280

1.

Prolidase deficiency: an inborn error of metabolism with major dermatological manifestations.

Der Kaloustian VM, Freij BJ, Kurban AK.

Dermatologica. 1982 May;164(5):293-304. No abstract available.

PMID:
7095220
2.

[Prolidase deficiency. Apropos of a peculiar case].

De Rijcke S, De Maubeuge J, Laporte M, Bron D, Hariga C, Ledoux M.

Ann Dermatol Venereol. 1989;116(4):309-12. Review. French. No abstract available.

PMID:
2675733
3.

Prolidase deficiency. A metabolic disorder presenting with dermatologic signs.

Freij BJ, Der Kaloustian VM.

Int J Dermatol. 1986 Sep;25(7):431-3. No abstract available.

PMID:
3771038
4.

Prolidase deficiency.

Pedersen PS, Christensen E, Brandt NJ.

Acta Paediatr Scand. 1983 Sep;72(5):785-8.

PMID:
6637477
5.

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.

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.

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
8.

Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer.

Ikeda K, Tohyama J, Tsujino S, Sato K, Oono T, Arata J, Endo F, Sakuragawa N.

Jpn J Hum Genet. 1997 Sep;42(3):401-8.

PMID:
12503186
9.

Prolidase deficiency associated with pathologic myopia.

Kiratli H, SatilmiƟ M.

Ophthalmic Genet. 1998 Mar;19(1):49-53.

PMID:
9587929
10.

Prolidase deficiency: case reports of two Argentinian brothers.

Cabrera HN, Giovanna PD, Bozzini NF, Forlino A.

Int J Dermatol. 2004 Sep;43(9):684-6. No abstract available.

PMID:
15357754
11.

Topical treatment of skin ulcers in prolidase deficiency.

Jemec GB, Moe AT.

Pediatr Dermatol. 1996 Jan-Feb;13(1):58-60.

PMID:
8919529
12.

Leg ulcers secondary to prolidase deficiency.

Trent JT, Kirsner RS.

Adv Skin Wound Care. 2004 Nov-Dec;17(9):468-72. Review. No abstract available.

PMID:
15632738
13.

Mental retardation in methemoglobinemia due to diaphorase deficiency.

Fialkow PJ, Browder JA, Sparkes RS, Motulsky AG.

N Engl J Med. 1965 Oct 14;273(16):840-5. No abstract available.

PMID:
4378489
14.

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.

15.

Metabolic faults and mental retardation.

Moseley V.

J S C Med Assoc. 1967 Jul;63(7):251-2. No abstract available.

PMID:
5233132
16.

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.

17.

Prolidase deficiency.

Kokturk A, Kaya TI, Ikizoglu G, Koca A.

Int J Dermatol. 2002 Jan;41(1):45-8. No abstract available.

PMID:
11895514
18.

[Screening for hereditary metabolic diseases in a group of children with a severe degree of intellectual defect].

Krasnopol'skaia KD, Draudin VA.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1975;75(4):571-3. Russian. No abstract available.

PMID:
813464
19.

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
20.

In-vitro responses to ascorbate and manganese in fibroblasts from a patient with prolidase deficiency and iminodipeptiduria: cell growth, prolidase activity and collagen metabolism.

Myara I, Charpentier C, Wolfrom C, Gautier M, Lemonnier A, Larregue M, Chamson A, Frey J.

J Inherit Metab Dis. 1983;6(1):27-31.

PMID:
6408304

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