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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 14, 2023
Anxiety in children with SMA - An underestimated problem
Heike Kölbel
Der Nervenarzt
|
March 30, 2023
[Update on drug treatment of spinal muscular atrophy]
Heike Kölbel, Tim Hagenacker
Frontiers in Neurology
|
May 29, 2019
Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients
Heike Kölbel, Denisa Hathazi, Matthew Jennings, et al.
Neuromuscular Disorders : NMD
|
May 13, 2017
Deep intronic variants introduce DMD pseudoexon in patient with muscular dystrophy
Ann-Kathrin Zaum, Burkhard Stüve, Andrea Gehrig, et al.
Molecular and Cellular Probes
|
January 26, 2019
HADHA and HADHB gene associated phenotypes - Identification of rare variants in a patient cohort by Next Generation Sequencing
Isabel Diebold, Ulrike Schön, Rita Horvath, et al.
Frontiers in Human Neuroscience
|
December 28, 2020
Long Term Follow-Up on Pediatric Cases With Congenital Myasthenic Syndromes-A Retrospective Single Centre Cohort Study
Adela Della Marina, Eva Wibbeler, Angela Abicht, et al.
Plos One
|
March 10, 2017
Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
Heike Kölbel, Berthold P Hauffa, Stefan A Wudy, et al.
Plos One
|
April 7, 2017
Correction: Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
Heike Kölbel, Berthold P Hauffa, Stefan A Wudy, et al.
Klinische Padiatrie
|
December 23, 2025
Chiari Malformation Type I with Compression of the Cervical Myelon as a Cause of Laryngomalacia
Anna Pauly, Mathis Steindor, Adela Della Marina, et al.
Children (Basel, Switzerland)
|
December 23, 2022
Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening
Heike Kölbel, Laura Modler, Astrid Blaschek, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 81) with videos related to
Sort By:
Page
of 9
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 14, 2023
Anxiety in children with SMA - An underestimated problem
Heike Kölbel
Der Nervenarzt
|
March 30, 2023
[Update on drug treatment of spinal muscular atrophy]
Heike Kölbel, Tim Hagenacker
Frontiers in Neurology
|
May 29, 2019
Identification of Candidate Protein Markers in Skeletal Muscle of Laminin-211-Deficient CMD Type 1A-Patients
Heike Kölbel, Denisa Hathazi, Matthew Jennings, et al.
Neuromuscular Disorders : NMD
|
May 13, 2017
Deep intronic variants introduce DMD pseudoexon in patient with muscular dystrophy
Ann-Kathrin Zaum, Burkhard Stüve, Andrea Gehrig, et al.
Molecular and Cellular Probes
|
January 26, 2019
HADHA and HADHB gene associated phenotypes - Identification of rare variants in a patient cohort by Next Generation Sequencing
Isabel Diebold, Ulrike Schön, Rita Horvath, et al.
Frontiers in Human Neuroscience
|
December 28, 2020
Long Term Follow-Up on Pediatric Cases With Congenital Myasthenic Syndromes-A Retrospective Single Centre Cohort Study
Adela Della Marina, Eva Wibbeler, Angela Abicht, et al.
Plos One
|
March 10, 2017
Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
Heike Kölbel, Berthold P Hauffa, Stefan A Wudy, et al.
Plos One
|
April 7, 2017
Correction: Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III
Heike Kölbel, Berthold P Hauffa, Stefan A Wudy, et al.
Klinische Padiatrie
|
December 23, 2025
Chiari Malformation Type I with Compression of the Cervical Myelon as a Cause of Laryngomalacia
Anna Pauly, Mathis Steindor, Adela Della Marina, et al.
Children (Basel, Switzerland)
|
December 23, 2022
Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening
Heike Kölbel, Laura Modler, Astrid Blaschek, et al.
Page
of 9