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W Padberg

Showing results (121-130 of 228) with videos related to

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Journal of Neurology|December 4, 2003
Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaintBarbara M Van Der Sluijs, Lies H Hoefsloot, George W Padberg, et al.
Langenbeck'S Archives of Surgery|January 28, 2019
Intra-abdominal sepsis: new definitions and current clinical standardsA Hecker, M Reichert, C J Reuß, et al.
Muscle & Nerve. Supplement|April 12, 2013
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Muscle & Nerve. Supplement|January 1, 1995
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Transplantation|August 1, 1986
Development of suppressor lymphocytes during acute rejection of rat cardiac allografts and preservation of suppression by anti-IL-2-receptor monoclonal antibodyT M Schneider, J W Kupiec-Weglinski, E Towpik, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|September 8, 2011
[Continuous local wound infusion with local anesthetics : For thoracotomy and major abdominal interventions]V Mann, S Mann, A Hecker, et al.
Genomics|June 15, 2005
Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouseBert van der Zwaag, J Peter H Burbach, Curt Scharfe, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophyHermien E Kan, Tom W J Scheenen, Marielle Wohlgemuth, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Genomics|January 1, 1994
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletionsC Wijmenga, J C van Deutekom, J E Hewitt, et al.
Pageof 23

Showing results (121-130 of 228) with videos related to

Sort By:
Pageof 23
Journal of Neurology|December 4, 2003
Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaintBarbara M Van Der Sluijs, Lies H Hoefsloot, George W Padberg, et al.
Langenbeck'S Archives of Surgery|January 28, 2019
Intra-abdominal sepsis: new definitions and current clinical standardsA Hecker, M Reichert, C J Reuß, et al.
Muscle & Nerve. Supplement|April 12, 2013
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Muscle & Nerve. Supplement|January 1, 1995
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Transplantation|August 1, 1986
Development of suppressor lymphocytes during acute rejection of rat cardiac allografts and preservation of suppression by anti-IL-2-receptor monoclonal antibodyT M Schneider, J W Kupiec-Weglinski, E Towpik, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|September 8, 2011
[Continuous local wound infusion with local anesthetics : For thoracotomy and major abdominal interventions]V Mann, S Mann, A Hecker, et al.
Genomics|June 15, 2005
Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouseBert van der Zwaag, J Peter H Burbach, Curt Scharfe, et al.
Neuromuscular Disorders : NMD|March 31, 2009
Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophyHermien E Kan, Tom W J Scheenen, Marielle Wohlgemuth, et al.
Human Molecular Genetics|November 25, 2000
Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticityP G van Overveld, R J Lemmers, G Deidda, et al.
Genomics|January 1, 1994
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletionsC Wijmenga, J C van Deutekom, J E Hewitt, et al.
Pageof 23