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W Padberg

Showing results (111-120 of 228) with videos related to

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American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
Journal of Neurology|February 25, 2005
Cognitive evaluation in adult patients with Möbius syndromeH T F M Verzijl, N van Es, H J C Berger, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Magnetic Resonance in Medicine|October 13, 2006
Intake of 13C-4 creatine enables simultaneous assessment of creatine and phosphocreatine pools in human skeletal muscle by 13C MR spectroscopyH E Kan, M van der Graaf, D W J Klomp, et al.
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Transplantation Proceedings|September 1, 2009
New-onset diabetes mellitus after renal transplantationM Eckhard, R A Schindler, F C Renner, et al.
Transplantation Proceedings|December 19, 2006
Immunoglobulin induction therapy in renal transplant recipients: Effects on immunoglobulin and regulatory antibody levelsA Staak, F Renner, C Suesal, et al.
The European Respiratory Journal|October 12, 2007
Keratinocyte growth factor prevents intra-alveolar oedema in experimental lung isograftsJ Sadovski, T Kuchenbuch, C Ruppert, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|September 29, 2021
[New WSES-AAST guidelines on trauma of the urogenital tract-Summary and comments]J Noll, F Coccolini, F Catena, et al.
Pageof 23

Showing results (111-120 of 228) with videos related to

Sort By:
Pageof 23
American Journal of Human Genetics|August 12, 1999
A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch familyH T Verzijl, B van den Helm, B Veldman, et al.
Muscle & Nerve. Supplement|April 12, 2013
On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophyG W Padberg, O F Brouwer, R J de Keizer, et al.
Journal of Neurology|February 25, 2005
Cognitive evaluation in adult patients with Möbius syndromeH T F M Verzijl, N van Es, H J C Berger, et al.
Human Genetics|April 1, 1994
Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genomeJ C van Deutekom, R P Bruyn, N van den Boorn, et al.
Magnetic Resonance in Medicine|October 13, 2006
Intake of 13C-4 creatine enables simultaneous assessment of creatine and phosphocreatine pools in human skeletal muscle by 13C MR spectroscopyH E Kan, M van der Graaf, D W J Klomp, et al.
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Transplantation Proceedings|September 1, 2009
New-onset diabetes mellitus after renal transplantationM Eckhard, R A Schindler, F C Renner, et al.
Transplantation Proceedings|December 19, 2006
Immunoglobulin induction therapy in renal transplant recipients: Effects on immunoglobulin and regulatory antibody levelsA Staak, F Renner, C Suesal, et al.
The European Respiratory Journal|October 12, 2007
Keratinocyte growth factor prevents intra-alveolar oedema in experimental lung isograftsJ Sadovski, T Kuchenbuch, C Ruppert, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|September 29, 2021
[New WSES-AAST guidelines on trauma of the urogenital tract-Summary and comments]J Noll, F Coccolini, F Catena, et al.
Pageof 23