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A Pekrun

Showing results (11-20 of 49) with videos related to

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European Journal of Pediatrics|January 1, 1989
The gamma-chain heterogeneity of haemoglobin F in German infantsA Pekrun, M Scharnetzky, M Gahr, et al.
Haematologica|August 28, 2001
Post-transcriptional effects of interleukin-3, interferon-gamma, erythropoietin and butyrate on in vitro hemoglobin chain synthesis in congenital hemolytic anemiaD Reinhardt, R Ridder, W Kugler, et al.
Deutsche Medizinische Wochenschrift (1946)|September 10, 1993
[Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia]A Pekrun, M Lakomek, W Eng, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1988
[Aplastic crises in hereditary spherocytosis]A Pekrun, H Eiffert, S W Eber, et al.
The Journal of Urology|January 1, 1994
Wilms tumor: the problem of diagnostic accuracy in children undergoing preoperative chemotherapy without histological tumor verificationG Zoeller, A Pekrun, M Lakomek, et al.
Acta Neuropathologica|January 1, 1990
Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiencyA Bardosi, S W Eber, M Hendrys, et al.
Annals of Hematology|August 1, 1993
Combined ankyrin and spectrin deficiency in hereditary spherocytosisA Pekrun, S W Eber, A Kuhlmey, et al.
Annals of Hematology|February 1, 1992
Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis testS W Eber, A Pekrun, A Neufeldt, et al.
British Journal of Urology|October 1, 1995
Staging problems in the pre-operative chemotherapy of Wilms' tumourG Zoeller, A Pekrun, M Lakomek, et al.
Human Mutation|April 11, 2001
Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) geneW Kugler, A Pekrun, P Laspe, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
European Journal of Pediatrics|January 1, 1989
The gamma-chain heterogeneity of haemoglobin F in German infantsA Pekrun, M Scharnetzky, M Gahr, et al.
Haematologica|August 28, 2001
Post-transcriptional effects of interleukin-3, interferon-gamma, erythropoietin and butyrate on in vitro hemoglobin chain synthesis in congenital hemolytic anemiaD Reinhardt, R Ridder, W Kugler, et al.
Deutsche Medizinische Wochenschrift (1946)|September 10, 1993
[Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia]A Pekrun, M Lakomek, W Eng, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|April 1, 1988
[Aplastic crises in hereditary spherocytosis]A Pekrun, H Eiffert, S W Eber, et al.
The Journal of Urology|January 1, 1994
Wilms tumor: the problem of diagnostic accuracy in children undergoing preoperative chemotherapy without histological tumor verificationG Zoeller, A Pekrun, M Lakomek, et al.
Acta Neuropathologica|January 1, 1990
Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiencyA Bardosi, S W Eber, M Hendrys, et al.
Annals of Hematology|August 1, 1993
Combined ankyrin and spectrin deficiency in hereditary spherocytosisA Pekrun, S W Eber, A Kuhlmey, et al.
Annals of Hematology|February 1, 1992
Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis testS W Eber, A Pekrun, A Neufeldt, et al.
British Journal of Urology|October 1, 1995
Staging problems in the pre-operative chemotherapy of Wilms' tumourG Zoeller, A Pekrun, M Lakomek, et al.
Human Mutation|April 11, 2001
Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) geneW Kugler, A Pekrun, P Laspe, et al.
Pageof 5