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Author/Creator Oldfors, Anders

1. A new muscle glycogen storage disease associated with glycogenin‐1 deficiency. Issue 6 (31st October 2014)

Authors:
Malfatti, Edoardo; Nilsson, Johanna; Hedberg‐Oldfors, Carola; Hernandez‐Lain, Aurelio; Michel, Fabrice; Dominguez‐Gonzalez, Cristina; Viennet, Gabriel; Akman, H. Orhan; Kornblum, Cornelia; Van den Bergh, Peter; Romero, Norma B.; Engel, Andrew G.; DiMauro, Salvatore; Oldfors, Anders
Journal:
Annals of neurology
Issue:
Volume 76:Issue 6(2014:Dec.)
Page Start:
891
Record Type:
Journal Article
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3. Cardiac arrest in Wilson's disease after curative liver transplantation: a life‐threatening complication of myocardial copper excess?. (8th January 2019)

Authors:
Bobbio, Emanuele; Forsgard, Niklas; Oldfors, Anders; Szamlewski, Piotr; Bollano, Entela; Andersson, Bert; Lingbrant, Marie; Bergh, Niklas; Karason, Kristjan; Polte, Christian L.
Journal:
ESC heart failure
Issue:
Volume 6:Number 1(2019)
Page Start:
228
Record Type:
Journal Article
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6. Cardiomyopathy as presenting sign of glycogenin‐1 deficiency—report of three cases and review of the literature. Issue 1 (7th October 2016)

Authors:
Hedberg‐Oldfors, Carola; Glamuzina, Emma; Ruygrok, Peter; Anderson, Lisa J.; Elliott, Perry; Watkinson, Oliver; Occleshaw, Chris; Abernathy, Malcolm; Turner, Clinton; Kingston, Nicola; Murphy, Elaine; Oldfors, Anders
Journal:
Journal of inherited metabolic disease
Issue:
Volume 40:Issue 1(2017)
Page Start:
139
Record Type:
Journal Article
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7. Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24. (1st February 2019)

Authors:
Hedberg-Oldfors, Carola; Abramsson, Alexandra; Osborn, Daniel P S; Danielsson, Olof; Fazlinezhad, Afsoon; Nilipour, Yalda; Hübbert, Laila; Nennesmo, Inger; Visuttijai, Kittichate; Bharj, Jaipreet; Petropoulou, Evmorfia; Shoreim, Azza; Vona, Barbara; Ahangari, Najmeh; López, Marcela Dávila; Doosti...
Journal:
Human molecular genetics
Issue:
Volume 28:Number 11(2019)
Page Start:
1919
Record Type:
Journal Article
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10. Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene. (4th May 2019)

Authors:
Meinert, Monika; Englund, Elisabet; Hedberg-Oldfors, Carola; Oldfors, Anders; Kornhall, Björn; Lundin, Catarina; Wittström, Elisabeth
Journal:
Ophthalmic genetics
Issue:
Volume 40:Number 3(2019)
Page Start:
227
Record Type:
Journal Article
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