메뉴 건너뛰기




Volumn 62, Issue 6, 2010, Pages 1031-1034

An Amish boy with recurrent ulcerations of the lower extremities, telangiectases of the hands, and chronic lung disease

Author keywords

chronic lung disease; immunodeficiency; leg ulcers; prolidase deficiency; skin; telangiectasia; ulcers

Indexed keywords

IMMUNOGLOBULIN A; IMMUNOGLOBULIN E; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M; OXYGEN; PROLINE DIPEPTIDASE;

EID: 77951891528     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jaad.2009.12.038     Document Type: Article
Times cited : (15)

References (19)
  • 1
    • 33645378758 scopus 로고    scopus 로고
    • A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome
    • Hershkovitz T., Hassoun G., Indelman M., Shlush L.I., Bergman R., Pollack S., et al. A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome. Clin Exp Dermatol 31 (2006) 435-440
    • (2006) Clin Exp Dermatol , vol.31 , pp. 435-440
    • Hershkovitz, T.1    Hassoun, G.2    Indelman, M.3    Shlush, L.I.4    Bergman, R.5    Pollack, S.6
  • 3
    • 0027439867 scopus 로고
    • Proline-dependent structural and biological properties of peptides and proteins
    • Yaron A., and Naider F. Proline-dependent structural and biological properties of peptides and proteins. Crit Rev Biochem Mol Biol 28 (1993) 31-81
    • (1993) Crit Rev Biochem Mol Biol , vol.28 , pp. 31-81
    • Yaron, A.1    Naider, F.2
  • 4
    • 0016258415 scopus 로고
    • A prolidase deficiency in man with iminopeptiduria
    • Powell G.F., Rasco M.A., and Maniscalco R.M. A prolidase deficiency in man with iminopeptiduria. Metabolism 23 (1974) 505-513
    • (1974) Metabolism , vol.23 , pp. 505-513
    • Powell, G.F.1    Rasco, M.A.2    Maniscalco, R.M.3
  • 5
    • 33751086222 scopus 로고    scopus 로고
    • Molecular characterization of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family
    • e58
    • Lupi A., Rossi A., Campari E., Pecora F., Lund A.M., Elcioglu N.H., et al. Molecular characterization of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family. J Med Genet 43 (2006) e58
    • (2006) J Med Genet , vol.43
    • Lupi, A.1    Rossi, A.2    Campari, E.3    Pecora, F.4    Lund, A.M.5    Elcioglu, N.H.6
  • 12
    • 32244437411 scopus 로고    scopus 로고
    • The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach
    • Viglio S., Annovazzi L., Conti B., Genta I., Perugini P., Zanone C., et al. The role of emerging techniques in the investigation of prolidase deficiency: from diagnosis to the development of a possible therapeutical approach. J Chromatogr B Analyt Technol Biomed Life Sci 832 (2006) 1-8
    • (2006) J Chromatogr B Analyt Technol Biomed Life Sci , vol.832 , pp. 1-8
    • Viglio, S.1    Annovazzi, L.2    Conti, B.3    Genta, I.4    Perugini, P.5    Zanone, C.6
  • 13
    • 0018382371 scopus 로고
    • Prolidase deficiency with imidodipeptiduria: a familial case with and without clinical symptoms
    • Isemura M., Hanyu T., Gejyo F., Nakazawa R., Igarashi R., Matsuo S., et al. Prolidase deficiency with imidodipeptiduria: a familial case with and without clinical symptoms. Clin Chim Acta 93 (1979) 401-407
    • (1979) Clin Chim Acta , vol.93 , pp. 401-407
    • Isemura, M.1    Hanyu, T.2    Gejyo, F.3    Nakazawa, R.4    Igarashi, R.5    Matsuo, S.6
  • 14
    • 84943987008 scopus 로고
    • Autosomal recessive prolidase deficiency: three patients with recalcitrant ulcers
    • Ogata A., Tanaka S., Tomoda T., Murayama E., Endo F., and Kikuchi I. Autosomal recessive prolidase deficiency: three patients with recalcitrant ulcers. Arch Dermatol 117 (1981) 689-697
    • (1981) Arch Dermatol , vol.117 , pp. 689-697
    • Ogata, A.1    Tanaka, S.2    Tomoda, T.3    Murayama, E.4    Endo, F.5    Kikuchi, I.6
  • 16
    • 0036886474 scopus 로고    scopus 로고
    • Therapeutic apheresis exchange in two patients with prolidase deficiency
    • Lupi A., Casado B., Soli M., Bertazzoni M., Annovazzi L., Viglio S., et al. Therapeutic apheresis exchange in two patients with prolidase deficiency. Br J Dermatol 147 (2002) 1237-1240
    • (2002) Br J Dermatol , vol.147 , pp. 1237-1240
    • Lupi, A.1    Casado, B.2    Soli, M.3    Bertazzoni, M.4    Annovazzi, L.5    Viglio, S.6
  • 18
    • 0033943005 scopus 로고    scopus 로고
    • Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency
    • Monafo V., Marseglia G.L., Maghnie M., Dyne K.M., and Cetta G. Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. Pediatr Dermatol 17 (2000) 227-230
    • (2000) Pediatr Dermatol , vol.17 , pp. 227-230
    • Monafo, V.1    Marseglia, G.L.2    Maghnie, M.3    Dyne, K.M.4    Cetta, G.5
  • 19
    • 0032738517 scopus 로고    scopus 로고
    • Corticosteroid treatment of prolidase deficiency skin lesions by inhibiting iminodipeptide-primed neutrophil superoxide generation
    • Yasuda K., Ogata K., Kariya K., Kodama H., Zhang J., Sugahara K., et al. Corticosteroid treatment of prolidase deficiency skin lesions by inhibiting iminodipeptide-primed neutrophil superoxide generation. Br J Dermatol 141 (1999) 846-851
    • (1999) Br J Dermatol , vol.141 , pp. 846-851
    • Yasuda, K.1    Ogata, K.2    Kariya, K.3    Kodama, H.4    Zhang, J.5    Sugahara, K.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.