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Artículos sobre la atransferrinemia
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| Molecular characterization of a case of atransferrinemia | ||
| Ernest Beutler, Terri Gelbart, Pauline Lee, Reneé Trevino, Mark A. Fernandez, and Virgil F. Fairbanks | ||
| Blood, 15 December 2000, Vol. 96, No. 13, pp. 4071-4074 | ||
| Molecular characterization of a third case of human atransferrinemia | ||
| A.S. Knisely, Terri Gelbart, and Ernest Beutler | ||
| Blood, 15 October 2004, Vol. 104, No. 8, pp. 2607 | ||
| Congenital atransferrinemia: a case report | ||
| LIN Guozhen, CHEN Le, WANG Wei, et al. | ||
| Chinese Journal of pediatrics, 2002. Volume 40, Number 2 February 16,pag 96 | ||
| Biochemical and genetic defects underlying human congenital hypotransferrinemia. | ||
| Goldwurm S, Casati C, Venturi N, Strada S, Santambrogio P, Indraccolo S, Arosio P, Cazzola M, Piperno A, Masera G, Biondi A. | ||
| Hematol J. 2000;1(6):390-8. | ||
| Congenital atransferrinemia | ||
| Hromec A, Payer J Jr, Killinger Z, Rybar I, Rovensky
J. I Medizinische Klinik, Komensky-Universitat Bratislava. |
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| Dtsch Med Wochenschr. 1994 May 6;119(18):663-6. | ||
| Congenital atransferrinemia in a 11-month-old child | ||
| Cap J, Lehotska V, Mayerova A. |
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| Cesk Pediatr. 1968 Oct;23(11):1020-5. | ||
| A family of congenital atransferrinemia. | ||
| Goya N, Miyazaki S, Kodate S, Ushio B. | ||
| Blood. 1972;40:239-245 | ||
| A case of congenital atransferrinemia | ||
| Sakata T. | ||
| Shonika Shinryo. 1969;32:1523 | ||
| Congenital atransferrinemia. A case report and review of the literature. | ||
| Hamill RL, Woods JC, Cook BA.Dept of Pathology, Tripler Army Medical Center, Honolulu, Hawaii 96859-5000. | ||
| Am J Clin Pathol. 1991 Aug;96(2):215-8. | ||
| Congenital transferrin deficiency |
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| Walbaum R. | ||
| Lille Med. 1971 Oct;16(8):1122-4. | ||
| Hereditary atransferrinemia | ||
| Loperena L, Dorantes S, Medrano E, Berron R, Vega L,
Cuaron A, Rodriguez C, Marquez JL. |
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| Bol Med Hosp Infant Mex. 1974 May-Jun;31(3):519-35 | ||
| Iron overload in hereditary atransferrinemia | ||
| Dorantes-Mesa S, Marquez JL, Valencia-Mayoral P. |
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| Bol Med Hosp Infant Mex. 1986 Feb;43(2):99-101. | ||
| Congenital atransferrinemia | ||
| HEILMEYER L, KELLER W, VIVELL O, BETKE K, WOEHLER F,
KEIDERLING W. |
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| Schweiz Med Wochenschr. 1961 Oct 7;91:1203 | ||
| Congenital atransferrinemia | ||
| Urabe A. Department of Medicine, Teikyo University Mizonokuchi
Hospital. |
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| Nippon Rinsho. 1991 Mar;49(3):634-6. | ||
| Studies on familial hypotransferrinemia: unique
clinical course and molecular pathology. |
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| Hayashi A, Wada Y, Suzuki T, Shimizu A.Osaka Medical
Center and Research Inst Maternal and Child Health |
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| Am J Hum Genet. 1993 Jul;53(1):201-13. | ||
| Replacement therapy for a patient with congenital atransferrinemia--therapeutic effect of apotansferrin | ||
| Kawakami T, Sone Y, Numajiri S, Sakata T. |
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| Rinsho Ketsueki. 1981 Nov;22(11):1708-13. | ||
| A case of atransferrinemia and 35 cases of hypotransferrinemia as determined by radioassay of total iron-binding capacity of the serum |
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| Saito H. |
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| Rinsho Ketsueki. 1975 Nov;16(11):1036-43 | ||
| Atransferrinemia Congénita: Revisión del cuadro clínico | ||
| GASTON MORATA, A. RODRIGUEZ CUARTERO | ||
| Sangre, 27 (4) : 538-541, 1982. | ||
| Sindrome nefrosica atransferrinemica | ||
| GIUSEPPE OLIVA et al. | ||
| Minerva Medica, N. 23 (21 MARZO 1968) | ||