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A Pekrun

Showing results (41-50 of 49) with videos related to

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European Journal of Pediatrics|September 1, 1991
Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activityS W Eber, A Pekrun, A Bardosi, et al.
Blood|October 15, 1995
Evidence for malignant transformation in acute myeloid leukemia at the level of early hematopoietic stem cells by cytogenetic analysis of CD34+ subpopulationsD Haase, M Feuring-Buske, S Könemann, et al.
Klinische Padiatrie|January 29, 2011
Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID)J S Kühl, K Schwarz, A Münch, et al.
Pediatric Radiology|April 12, 2001
Somatostatin receptor scintigraphy in the management of cerebral malignant ectomesenchymoma: a case reportM Papós, A Pekrun, J W Herms, et al.
Annals of Hematology|June 10, 1998
Hemoglobin F in myelodysplastic syndromeD Reinhardt, D Haase, C Schoch, et al.
Transfusion|September 30, 1999
Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patientsT J Legler, S W Eber, M Lakomek, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Klinische Padiatrie|April 20, 2012
[GATA1-mutation associated leukemia in children with trisomy 21 mosaic]D Reinhardt, K Reinhardt, C Neuhoff, et al.
Nature Genetics|June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosisS W Eber, J M Gonzalez, M L Lux, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
European Journal of Pediatrics|September 1, 1991
Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activityS W Eber, A Pekrun, A Bardosi, et al.
Blood|October 15, 1995
Evidence for malignant transformation in acute myeloid leukemia at the level of early hematopoietic stem cells by cytogenetic analysis of CD34+ subpopulationsD Haase, M Feuring-Buske, S Könemann, et al.
Klinische Padiatrie|January 29, 2011
Hyperbilirubinemia and rapid fatal hepatic failure in severe combined immunodeficiency caused by adenosine deaminase deficiency (ADA-SCID)J S Kühl, K Schwarz, A Münch, et al.
Pediatric Radiology|April 12, 2001
Somatostatin receptor scintigraphy in the management of cerebral malignant ectomesenchymoma: a case reportM Papós, A Pekrun, J W Herms, et al.
Annals of Hematology|June 10, 1998
Hemoglobin F in myelodysplastic syndromeD Reinhardt, D Haase, C Schoch, et al.
Transfusion|September 30, 1999
Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patientsT J Legler, S W Eber, M Lakomek, et al.
Neuropediatrics|March 6, 2004
CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two childrenK Rostasy, R Kolb, D Pohl, et al.
Klinische Padiatrie|April 20, 2012
[GATA1-mutation associated leukemia in children with trisomy 21 mosaic]D Reinhardt, K Reinhardt, C Neuhoff, et al.
Nature Genetics|June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosisS W Eber, J M Gonzalez, M L Lux, et al.
Pageof 5