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M Abramowicz

Showing results (71-80 of 77) with videos related to

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Lancet (London, England)|May 9, 1970
Controlled trial of azathioprine in children with nephrotic syndrome. A report for the international study of kidney disease in childrenM Abramowicz, H L Barnett, C M Edelmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 10, 2025
Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathyR van Heurck, E B Hammar, D Ville, et al.
Human Mutation|January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseasesJ Poncin, R Abs, B Velkeniers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicingL M Messiaen, T Callens, K J Roux, et al.
Clinical Genetics|May 24, 2008
Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasiaK Brakensiek, H Frye-Boukhriss, M Mälzer, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 23, 2009
Thrombophilic factors do not predict outcomes in renal transplant recipients under prophylactic acetylsalicylic acidL Ghisdal, N Broeders, K-M Wissing, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 9, 2016
Genome-Wide Association Study of Acute Renal Graft RejectionL Ghisdal, C Baron, Y Lebranchu, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Lancet (London, England)|May 9, 1970
Controlled trial of azathioprine in children with nephrotic syndrome. A report for the international study of kidney disease in childrenM Abramowicz, H L Barnett, C M Edelmann, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 10, 2025
Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathyR van Heurck, E B Hammar, D Ville, et al.
Human Mutation|January 15, 1999
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseasesJ Poncin, R Abs, B Velkeniers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2001
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicingL M Messiaen, T Callens, K J Roux, et al.
Clinical Genetics|May 24, 2008
Detection of a significant association between mutations in the ACVRL1 gene and hepatic involvement in German patients with hereditary haemorrhagic telangiectasiaK Brakensiek, H Frye-Boukhriss, M Mälzer, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 23, 2009
Thrombophilic factors do not predict outcomes in renal transplant recipients under prophylactic acetylsalicylic acidL Ghisdal, N Broeders, K-M Wissing, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 9, 2016
Genome-Wide Association Study of Acute Renal Graft RejectionL Ghisdal, C Baron, Y Lebranchu, et al.
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