Familial hyperprolinemia with nephropathy
Ortuño Mirete, J.; Guardiola Vicente, J.M.; Botella García, J.
Revista Clinica Espanola 118(2): 141-150
1970
ISSN/ISBN: 0014-2565 PMID: 5486371 Document Number: 20873
Document emailed within 1 workday
Related Documents
Nichifor, E.; Balea, M.; Rusu, G.; Melencu, M.; Ghiordănescu, N.; Cristescu, I.; Dovlete, C.; Sonoc, S. 1985: Studies on the familial character of endemic Balkan nephropathy. Possible role of the toxic hydric factor in the determination of "familial agglomerations" in endemic Balkan nephropathy Medecine Interne 23(3): 229-237Pohorecka-Zagroba, L.; Twardowski, Z. 1974: Familial nephropathy in the light of observed cases Polski Tygodnik Lekarski 29(33): 1433-1435
De la Cueva Martín, R.; Aznar Lucea, J. 1972: Familial hematuric nephropathy with deafness (Alport's syndrome) Revista Clinica Espanola 125(4): 357-360
Oksanen, A.; Sittnikow, K. 1972: Familial nephropathy with secondary hyperparathyroidism in three young dogs Nordisk Veterinaermedicin 24(5): 278-280
Badilla, A.; Rojas, C. 2001: Familial gout and nephropathy in a young woman. Report of one case Revista Medica de Chile 129(6): 666-670
Onenli-Mungan, N.; Yüksel, B.; Elkay, Mürüvet.; Topaloğlu, A.Kemal.; Baykal, T.; Ozer, Güler. 2004: Type II hyperprolinemia: a case report Turkish Journal of Pediatrics 46(2): 167-169
Fillastre, J.P.; Marx, P.; Laumonier, R.; Métayer, J.; Dubois, D.; Mallet, E. 1974: Familial chronic interstitial nephropathy and retinal dystrophy (Senior-Loken syndrome) La Nouvelle Presse Medicale 3(6): 309-312
1987: A 45-year-old man with uremia caused by familial non-filial nephropathy and aortic insufficiency corrected with a prosthesis Revista Clinica Espanola 181(9): 516-526
Koivisto, V.; Groop, P.H.; Huttunen, N.P.; Kivekäs, J.; Pasternack, A.; Uusitupa, M.; Viikari, J. 1997: Diabetic nephropathy--screening, follow-up and treatment. Nephropathy Study Groups of the Finnish Diabetes Organization Nordisk Medicin 112(5): 154-162
Kojima, H.; Ohi, H.; Miyaji, H.; Seki, M.; Fujita, T.; Hatano, M. 1987: Localization of C3d in renal tissues of patients with membranous nephropathy and IgA nephropathy Nihon Jinzo Gakkai Shi 29(9): 1161-1165
Recagno de Rousse, A.; Kaswan, E.; Pinto, J.A. 1978: Tropical parasitic nephropathy: bilharzial nephropathy. Preliminary communication G.E.N 32(4): 381-386
Taube, D.; Brown, Z.; Williams, D.G. 1984: Impaired lymphocyte and suppressor cell function in minimal change nephropathy, membranous nephropathy and focal glomerulosclerosis Clinical Nephrology 22(4): 176-182
Beukhof, J.R.; Kardaun, O.; Ockhuizen, T.; van der Hem, G.K. 1987: Kidney survival in IgA nephropathy: multiple regression analysis of genetically differing subpopulations--is IgA nephropathy a real disease entity? Seminars in Nephrology 7(4): 367-369
Katagiri, M.; Kida, H.; Naitou, T.; Takasawa, K.; Takeda, S.; Yoshimura, M.; Yokoyama, H.; Koshino, Y.; Abe, T.; Hattori, N. 1988: Clinico-pathological characteristics of IgA nephropathy with acute onset: comparative study of IgA nephropathy with cryptogenic onset and purpura nephritis Nihon Jinzo Gakkai Shi 30(1): 1-7
Yoshikawa, N.; Ito, H.; Sakai, T.; Takekoshi, Y.; Honda, M.; Awazu, M.; Ito, K.; Iitaka, K.; Koitabashi, Y.; Yamaoka, K.; Nakagawa, K.; Nakamura, H.; Matsuyama, S.; Seino, Y.; Takeda, N.; Hattori, S.; Ninomiya, M. 1997: A prospective controlled study of sairei-to in childhood IgA nephropathy with focal/minimal mesangial proliferation. Japanese Pediatric IgA Nephropathy Treatment Study Group Nihon Jinzo Gakkai Shi 39(5): 503-506
Krapivner, S.R.; Malyshev, P.P.; Rozhkova, T.A.; Potaraus, A.B.; Kukharchuk, V.V.; Bochkov, V.N. 2000: Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100 Terapevticheskii Arkhiv 72(4): 9-12
Li, N.; Boulay, M. 2010: Individual, familial and extra-familial factors associated with premarital sex among Bangladeshi male adolescents Sexual Health 7(4): 471-477
Akulenko, L.V.; Nikogosian, S.O.; Zhordaniia, K.I.; Kozachenko, V.P. 1991: Clinical course of the disease in familial and non-familial forms of serous cystadenocarcinoma of the ovary Akusherstvo i Ginekologiia 9: 58-60
Glueck, C.J.; Gartside, P.; Fallat, R.W.; Sielski, J.; Steiner, P.M. 1976: Longevity syndromes: familial hypobeta and familial hyperalpha lipoproteinemia Journal of Laboratory and Clinical Medicine 88(6): 941-957
Ganer, A.; Knobel, B.; Fryd, C.H.; Rachmilewitz, E.A. 1981: Dapsone-induced methemoglobinemia and hemolysis in the presence of familial hemoglobinopathy Hasharon and familial methemoglobin reductase deficiency Israel Journal of Medical Sciences 17(8): 703-704