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Results:
1-13
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Results: 13
Authors:
Misgeld, E
Gattermann, N
Wehmeier, A
Weiland, C
Peters, U
Kohne, E
Citation: E. Misgeld et al., Hemoglobinopathy York [beta 146 (HC3] His double right arrow Pro]: first report of a family history, ANN HEMATOL, 80(6), 2001, pp. 365-367
Authors:
Maywald, O
Galm, O
Fabry, U
Kohne, E
Osieka, R
Citation: O. Maywald et al., Uncommon cause of polycythemia in a pregnant female, MED KLIN, 96(1), 2001, pp. 45-49
Authors:
Cario, H
Stahnke, K
Sander, S
Kohne, E
Citation: H. Cario et al., Epidemiological situation and treatment of patients with thalassemia majorin Germany: results of the German multicenter beta-thalassemia study, ANN HEMATOL, 79(1), 2000, pp. 7-12
Authors:
Goldbeck, L
Baving, A
Kohne, E
Citation: L. Goldbeck et al., Psychosocial aspects of beta-thalassemia: Distress, coping and adherence., KLIN PADIAT, 212(5), 2000, pp. 254-259
Authors:
Mockenhaupt, FP
Rong, B
Gunther, M
Beck, S
Till, H
Kohne, E
Thompson, WNA
Bienzle, U
Citation: Fp. Mockenhaupt et al., Anaemia in pregnant Ghanaian women: importance of malaria, iron deficiency, and haemoglobinopathies, T RS TROP M, 94(5), 2000, pp. 477-483
Authors:
Buck, C
Thon, A
Wolf, A
Kohne, E
Holl, RW
Citation: C. Buck et al., Diagnosis of diabetes mellitus in cystic fibrosis (CF) - role of blood sugar, HbA(1c) and oral glucose tolerance test, MONATS KIND, 148(7), 2000, pp. 698-701
Authors:
Vetter, B
Neu-Yilik, G
Kohne, E
Arnold, R
Sinha, P
Gaedicke, G
Ivancevic, V
Kulozik, AE
Citation: B. Vetter et al., Dominant beta-thalassaemia: a highly unstable haemoglobin is caused by a novel 6 bp deletion of the beta-globin gene, BR J HAEM, 108(1), 2000, pp. 176-181
Authors:
Schulz, AS
Urban, J
Gessler, P
Behnisch, W
Kohne, E
Heymer, B
Citation: As. Schulz et al., Anaemia, thrombocytopenia and coagulopathy due to occult diffuse infantilehaemangiomatosis of spleen and pancreas, EUR J PED, 158(5), 1999, pp. 379-383
Authors:
Cario, H
Stahnke, K
Kohne, E
Citation: H. Cario et al., b-thalassemia in Germany - Results of the cooperative beta-thalassemia study, KLIN PADIAT, 211(6), 1999, pp. 431-437
Authors:
Willig, TN
Niemeyer, CM
Leblanc, T
Tiemann, C
Robert, A
Budde, J
Lambiliotte, A
Kohne, E
Souillet, G
Eber, S
Stephan, JL
Girot, R
Bordigoni, P
Cornu, G
Blanche, S
Guillard, JM
Mohandas, N
Tchernia, G
Citation: Tn. Willig et al., Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anemia patients, PEDIAT RES, 46(5), 1999, pp. 553-561
Authors:
Heimpel, H
Maier, K
Kohne, E
Citation: H. Heimpel et al., Congenital dyserythropoietic anemias: clinical manifestations and new observations on epidemiology, pathogenesis and therapy, MONATS KIND, 147(11), 1999, pp. 992-999
Authors:
Cario, H
Bode, H
Gustavsson, P
Dahl, N
Kohne, E
Citation: H. Cario et al., A microdeletion syndrome due to a 3-Mb deletion on 19q13.2 - Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation, CLIN GENET, 55(6), 1999, pp. 487-492
Authors:
Cario, H
Holl, RW
Kohne, E
Citation: H. Cario et al., Glucose intolerance in patients with thalassemia major: Insulin resistanceand hyperproinsulinemia, J PED END M, 11, 1998, pp. 953-955
Risultati:
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