Enzyme induction in hereditary spherocytosis using barbiturate
Tilz, G.P.
Medizinische Klinik 67(6): 193-194
1972
ISSN/ISBN: 0025-8458 PMID: 5027813 Document Number: 56015
Document emailed within 1 workday
Related Documents
Ideguchi, H. 1996: Hereditary spherocytosis Nihon Rinsho. Japanese Journal of Clinical Medicine 54(9): 2478-2483Agarwal, M.B.; Kumud, P.M.; Mehta, B.C. 1979: Hereditary spherocytosis in a neonate Indian Pediatrics 16(4): 359-361
Kwiatkowska, J. 1971: Erythrocyte metabolism in hereditary spherocytosis Acta Haematologica Polonica 2(2): 187-193
Yamada, H.; Ishimoto, M.; Hirayama, E.K.; Negishi, H.; Okuyama, K.; Sagawa, T.; Fujimoto, S. 1996: The management of pregnancy with hereditary spherocytosis Nihon Sanka Fujinka Gakkai Zasshi 48(1): 73-76
Santoso, F.X.; Sukardi; Permono, B.; Netty, R.H.; Untario, S. 1988: Hereditary spherocytosis: a clinical experience Paediatrica Indonesiana 28(1-2): 27-35
Rozier, J.C. 1971: Sporadic cases of hereditary spherocytosis North Carolina Medical Journal 32(4): 136-140
Pekrun, A.; Eiffert, H.; Eber, S.W.; Schröter, W. 1988: Aplastic crises in hereditary spherocytosis Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 136(4): 173-175
Vargas, L.; Messen, S.; Hubach, E.; García, H. 1987: Hereditary spherocytosis in the neonatal period Revista Chilena de Pediatria 58(1): 61-65
Tischendorf, F.W. 1983: Anemia and icterus: hereditary spherocytosis and ovalocytosis Die Medizinische Welt 34(38): 1031
McFetridge, L.; McAloon, J.; Hughes, J. 2006: Neonatal diagnostic difficulty in hereditary spherocytosis Irish Medical Journal 99(6): 189
Güngör, A.; Yaralı, Nşe.; Fettah, A.; Ok-Bozkaya, İkbal.; Özbek, Nık.; Kara, A. 2018: Hereditary spherocytosis: Retrospective evaluation of 65 children Turkish Journal of Pediatrics 60(3): 264-269
Das, M.R.; Ananthakrishnan, S. 2005: Hereditary spherocytosis in a family from Tamil Nadu Indian Pediatrics 42(6): 610-611
Agnifili, A.; Carducci, G.; Gola, P.; Mancini, E.; Marino, M.; Verzaro, R.; Ibi, I. 1998: Juvenile polyposis coli associated with hereditary spherocytosis Minerva Chirurgica 53(10): 811-817
Jonte, F.; Ramírez, A.; Medina, J.; García Gala, J.; Rosón, C.; Corte, J.R.; Vargas, M.; Pérez Lozana, L. 1995: Hereditary spherocytosis: clinical characteristics and treatment with splenectomy Sangre 40(1): 45-48
Fernández Fuertes, I.; Sureda, A.; Villarrubia, J.; Pascual, J.; Navarro, J.L. 1989: The modified "pink test" in the diagnosis of hereditary spherocytosis Sangre 34(6): 509-513
Pavón Morán, V.; Estrada del Cueto, M.; Fernández Delgado, N.; Sánchez Damas, M.; Vergara Rivero, R.; González Otero, A.; Vilorio Barreras, P.; Svarch, E. 2000: Effectiveness of partial splenectomy in the treatment of hereditary spherocytosis Revista de Investigacion Clinica; Organo del Hospital de Enfermedades de la Nutricion 52(3): 229-233
Mamatieva, A.A. 1975: Clinico-laboratory parallels in hereditary spherocytosis in children Pediatriia 6: 60-65
Fjaerli, H.O.; Vogt, H.; Bruu, A.L. 1991: Human parvovirus B19 as the cause of aplastic crisis in hereditary spherocytosis Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 111(22): 2735-2737
Moore, A.; Sherman, M.M.; Strongin, M.J. 1976: Hereditary spherocytosis with hemolytic crisis during pregnancy. Treatment by splenectomy Obstetrics and Gynecology 47(1): 19S-21S
Meyerstein, N.; Yirmiahu, T.; Zmora, E.; Dvilansky, A.; Gabriel, A.; Khoda, J. 1983: The acidified glyceral lysis test for hereditary spherocytosis and other anemias Harefuah 104(5): 165-167