Search research articles
Contact Us
Filters
Showing results (41-50 of 173) with videos related to
Page
of 18
Sort By:
Pharmacoeconomics
|
December 14, 2022
Caregiver Burden of Spinal Muscular Atrophy: A Systematic Review
Erik Landfeldt, Sophia Abner, Astrid Pechmann, et al.
Molecular and Cellular Probes
|
November 15, 2013
High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency
Maria de los Angeles Beytía, Gabriele Dekomien, Sabine Hoffjan, et al.
Journal of Neuromuscular Diseases
|
January 11, 2021
Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec -A Single Centre Experience
Johannes Friese, Stephanie Geitmann, Dorothea Holzwarth, et al.
The Patient
|
February 5, 2019
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic Review
Erik Landfeldt, Josefin Edström, Cecilia Jimenez-Moreno, et al.
Arthritis Research & Therapy
|
October 31, 2012
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathy
Nils Venhoff, Dirk Lebrecht, Dietmar Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 14, 2021
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiency
Jan Schönberger, Matthias Eckenweiler, Kerstin Alexandra Klotz, et al.
Developmental Medicine and Child Neurology
|
March 18, 2006
'Why do children with cerebral palsy discontinue therapy with botulinum toxin A?'
Michaela Linder-Lucht, Janbernd Kirschner, Jochen Herrmann, et al.
Antiviral Therapy
|
March 4, 2014
Zidovudine induces visceral mitochondrial toxicity and intra-abdominal fat gain in a rodent model of lipodystrophy
Ulrich A Walker, Dirk Lebrecht, Wilfried Reichard, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseases
Sunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Neuropediatrics
|
June 20, 2017
Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature
David C Schorling, Tobias Dietel, Christina Evers, et al.
Page
of 18
Search research articles
Search
Showing results (41-50 of 173) with videos related to
Sort By:
Page
of 18
Pharmacoeconomics
|
December 14, 2022
Caregiver Burden of Spinal Muscular Atrophy: A Systematic Review
Erik Landfeldt, Sophia Abner, Astrid Pechmann, et al.
Molecular and Cellular Probes
|
November 15, 2013
High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiency
Maria de los Angeles Beytía, Gabriele Dekomien, Sabine Hoffjan, et al.
Journal of Neuromuscular Diseases
|
January 11, 2021
Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec -A Single Centre Experience
Johannes Friese, Stephanie Geitmann, Dorothea Holzwarth, et al.
The Patient
|
February 5, 2019
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic Review
Erik Landfeldt, Josefin Edström, Cecilia Jimenez-Moreno, et al.
Arthritis Research & Therapy
|
October 31, 2012
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathy
Nils Venhoff, Dirk Lebrecht, Dietmar Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 14, 2021
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiency
Jan Schönberger, Matthias Eckenweiler, Kerstin Alexandra Klotz, et al.
Developmental Medicine and Child Neurology
|
March 18, 2006
'Why do children with cerebral palsy discontinue therapy with botulinum toxin A?'
Michaela Linder-Lucht, Janbernd Kirschner, Jochen Herrmann, et al.
Antiviral Therapy
|
March 4, 2014
Zidovudine induces visceral mitochondrial toxicity and intra-abdominal fat gain in a rodent model of lipodystrophy
Ulrich A Walker, Dirk Lebrecht, Wilfried Reichard, et al.
Orphanet Journal of Rare Diseases
|
October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseases
Sunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Neuropediatrics
|
June 20, 2017
Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature
David C Schorling, Tobias Dietel, Christina Evers, et al.
Page
of 18