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M De Paepe

Showing results (31-40 of 48) with videos related to

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Archives of Gynecology and Obstetrics|December 29, 2000
Pain relief in labour by transcutaneous electrical nerve stimulation (TENS)J T van der Spank, D C Cambier, H M De Paepe, et al.
Journal of Medical Genetics|April 1, 1991
Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiencyI M Buntinx, P J Willems, S E Spitaels, et al.
Pediatric Radiology|November 3, 1998
Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?G R Mortier, L M Messiaen, M Espeel, et al.
International Journal of Cardiology|December 1, 2005
Primary impairment of left ventricular function in Marfan syndromeJulie F De Backer, Daniel Devos, Patrick Segers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 10, 1981
Plasma vitamin A in haemodialysis patientsV O De Bevere, M De Paepe, A P De Leenheer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1992
Diagnostic criteria of analgesic nephropathy in patients with end-stage renal failure: results of the Belgian studyM M Elseviers, V Bosteels, P Cambier, et al.
Nature Medicine|February 2, 2000
Genetic correction of sickle cell disease: insights using transgenic mouse modelsM J Blouin, H Beauchemin, A Wright, et al.
Kidney International|March 1, 1996
Hepatitis C virus in a hemodialysis unit: molecular evidence for nosocomial transmissionL Stuyver, H Claeys, A Wyseur, et al.
Genesis (New York, N.Y. : 2000)|August 12, 2008
Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutionsB L Callewaert, B L Loeys, C Casteleyn, et al.
Orphanet Journal of Rare Diseases|February 28, 2013
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneitySmail Hadj-Rabia, Bert L Callewaert, Emmanuelle Bourrat, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Archives of Gynecology and Obstetrics|December 29, 2000
Pain relief in labour by transcutaneous electrical nerve stimulation (TENS)J T van der Spank, D C Cambier, H M De Paepe, et al.
Journal of Medical Genetics|April 1, 1991
Neonatal Marfan syndrome with congenital arachnodactyly, flexion contractures, and severe cardiac valve insufficiencyI M Buntinx, P J Willems, S E Spitaels, et al.
Pediatric Radiology|November 3, 1998
Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?G R Mortier, L M Messiaen, M Espeel, et al.
International Journal of Cardiology|December 1, 2005
Primary impairment of left ventricular function in Marfan syndromeJulie F De Backer, Daniel Devos, Patrick Segers, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 10, 1981
Plasma vitamin A in haemodialysis patientsV O De Bevere, M De Paepe, A P De Leenheer, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1992
Diagnostic criteria of analgesic nephropathy in patients with end-stage renal failure: results of the Belgian studyM M Elseviers, V Bosteels, P Cambier, et al.
Nature Medicine|February 2, 2000
Genetic correction of sickle cell disease: insights using transgenic mouse modelsM J Blouin, H Beauchemin, A Wright, et al.
Kidney International|March 1, 1996
Hepatitis C virus in a hemodialysis unit: molecular evidence for nosocomial transmissionL Stuyver, H Claeys, A Wyseur, et al.
Genesis (New York, N.Y. : 2000)|August 12, 2008
Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutionsB L Callewaert, B L Loeys, C Casteleyn, et al.
Orphanet Journal of Rare Diseases|February 28, 2013
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneitySmail Hadj-Rabia, Bert L Callewaert, Emmanuelle Bourrat, et al.
Pageof 5