1. A child with myoclonus-dystonia (DYT11) misdiagnosed as atypical opsoclonus myoclonus syndrome. (November 2015) Authors: Drivenes, Bergitte; Born, Alfred Peter; Ek, Jakob; Dunoe, Morten; Uldall, Peter Vilhelm Journal: European journal of paediatric neurology Issue: Volume 19:Number 6(2015:Nov.) Page Start: 719 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A mitochondrial tRNAMet mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood. (January 2015) Authors: Born, Alfred Peter; Duno, Morten; Rafiq, Jabin; Risom, Lotte; Wibrand, Flemming; Østergaard, Elsebet; Vissing, John Journal: European journal of paediatric neurology Issue: Volume 19:Number 1(2015:Jan.) Page Start: 69 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Basilar Artery Thrombosis in a Child Treated With Intravenous Tissue Plasminogen Activator and Endovascular Mechanical Thrombectomy. (November 2013) Authors: Fink, Jakob; Sonnenborg, Laura; Larsen, Line Lunde; Born, Alfred Peter; Holtmannspötter, Markus; Kondziella, Daniel Journal: Journal of child neurology Issue: Volume 28:Number 11(2013) Page Start: 1521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Children and adolescents previously treated with glucocorticoids display lower verbal intellectual abilities. (23rd April 2015) Authors: Holm, Sara Krøis; Vestergaard, Martin; Madsen, Kathrine Skak; Baaré, William F.C.; Hammer, Trine Bjørg; Born, Alfred Peter; Siebner, Hartwig R.; Paulson, Olaf B.; Uldall, Peter V. Journal: Acta pædiatrica Issue: Volume 104:Number 8(2015:Aug.) Page Start: 784 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. EEG with extreme delta brush in young female with methotrexate neurotoxicity supports NMDA receptor involvement. (September 2017) Authors: Schmidt, Lisbeth Samsø; Kjær, Troels W.; Schmiegelow, Kjeld; Born, Alfred Peter Journal: European journal of paediatric neurology Issue: Volume 21:Number 5(2017:Sep.) Page Start: 795 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Fetal acetylcholine receptor inactivation syndrome: A myopathy due to maternal antibodies. Issue 1 (February 2015) Authors: Hacohen, Yael; Jacobson, Leslie W.; Byrne, Susan; Norwood, Fiona; Lall, Abhimanu; Robb, Stephanie; Dilena, Robertino; Fumagalli, Monica; Born, Alfred Peter; Clarke, Debbie; Lim, Ming; Vincent, Angela; Jungbluth, Heinz Journal: Neurology Issue: Volume 2:Issue 1(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Infections seem to be more frequent before onset of pediatric multiple sclerosis: A Danish nationwide nested case–control study. (May 2019) Authors: Boesen, Magnus Spangsberg; Koch-Henriksen, Nils; Thygesen, Lau Caspar; Eriksson, Frank; Greisen, Gorm; Born, Alfred Peter; Blinkenberg, Morten; Uldall, Peter Vilhelm; Magyari, Melinda Journal: Multiple sclerosis Issue: Volume 25:Number 6(2019) Page Start: 783 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. LAMA2‐related myopathy: Frequency among congenital and limb‐girdle muscular dystrophies. Issue 4 (13th August 2015) Authors: Løkken, Nicoline; Born, Alfred Peter; Duno, Morten; Vissing, John Journal: Muscle & nerve Issue: Volume 52:Issue 4(2015:Oct.) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Metabolic assessment in children with neuromuscular disorders shows risk of liver enlargement, steatosis and fibrosis. (12th January 2023) Authors: Naume, Marie Mostue; Jørgensen, Marianne Hørby; Høi‐Hansen, Christina Engel; Born, Alfred Peter; Vissing, John; Borgwardt, Lise; Stærk, Dorte Marianne Rohde; Ørngreen, Mette Cathrine Journal: Acta pædiatrica Issue: Volume 112:Number 4(2023) Page Start: 846 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature. Issue 3 (20th January 2015) Authors: Ostergaard, Elsebet; Weraarpachai, Woranontee; Ravn, Kirstine; Born, Alfred Peter; Jønson, Lars; Duno, Morten; Wibrand, Flemming; Shoubridge, Eric A; Vissing, John Journal: Journal of medical genetics Issue: Volume 52:Issue 3(2015) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗