Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
|
|
|
4.
|
|
|
|
5.
|
|
|
|
6.
|
|
|
|
7.
|
|
|
|
8.
|
|
|
|
9.
|
|
|
|
10.
|
|
|
|
11.
|
|
|
|
12.
|
|
|
|
13.
|
|
|
|
14.
|
Erratum to: The presence of anaemia negatively influences survival in patients with POLG disease. [electronic resource] by
- Hikmat, Omar
- Tzoulis, Charalampos
- Klingenberg, Claus
- Rasmussen, Magnhild
- Tallaksen, Chantal M E
- Brodtkorb, Eylert
- Fiskerstrand, Torunn
- McFarland, Robert
- Rahman, Shamima
- Bindoff, Laurence A
Publication details: Journal of inherited metabolic disease 01 2018
In:
Journal of inherited metabolic disease vol. 41
Availability: No items available.
|
|
|
15.
|
The presence of anaemia negatively influences survival in patients with POLG disease. [electronic resource] by
- Hikmat, Omar
- Tzoulis, Charalampos
- Klingenberg, Claus
- Rasmussen, Magnhild
- Tallaksen, Chantal M E
- Brodtkorb, Eylert
- Fiskerstrand, Torunn
- McFarland, Robert
- Rahman, Shamima
- Bindoff, Laurence A
Producer: 20180607
In:
Journal of inherited metabolic disease vol. 40
Availability: No items available.
|
|
|
16.
|
Clinical and psychosocial follow-up study of children treated with extracorporeal membrane oxygenation. [electronic resource] by
- Wagner, Kari
- Risnes, Ivar
- Berntsen, Torhild
- Skarbø, Anne-Britt
- Ramberg, Brith
- Vandvik, Inger Helene
- Rasmussen, Magnhild
- Nome, Terje
- Olsen, Ketil Berg
- Svennevig, Jan Ludvig
Producer: 20071221
In:
The Annals of thoracic surgery vol. 84
Availability: No items available.
|
|
|
17.
|
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. [electronic resource] by
- Pedurupillay, Christeen Ramane J
- Amundsen, Silja S
- Barøy, Tuva
- Rasmussen, Magnhild
- Blomhoff, Anne
- Stadheim, Barbro Fossøy
- Ørstavik, Kristin
- Holmgren, Asbjørn
- Iqbal, Tahir
- Frengen, Eirik
- Misceo, Doriana
- Strømme, Petter
Producer: 20180125
In:
Neuromuscular disorders : NMD vol. 26
Availability: No items available.
|
|
|
18.
|
A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13. [electronic resource] by
- Barøy, Tuva
- Pedurupillay, Christeen Ramane J
- Bliksrud, Yngve T
- Rasmussen, Magnhild
- Holmgren, Asbjørn
- Vigeland, Magnus D
- Hughes, Timothy
- Brink, Maaike
- Rodenburg, Richard
- Nedregaard, Bård
- Strømme, Petter
- Frengen, Eirik
- Misceo, Doriana
Producer: 20170210
In:
European journal of medical genetics vol. 59
Availability: No items available.
|
|
|
19.
|
'North Sea' progressive myoclonus epilepsy: phenotype of subjects with GOSR2 mutation. [electronic resource] by
- Boissé Lomax, Lysa
- Bayly, Marta A
- Hjalgrim, Helle
- Møller, Rikke S
- Vlaar, Annemarie M
- Aaberg, Kari M
- Marquardt, Iris
- Gandolfo, Luke C
- Willemsen, Michèl
- Kamsteeg, Erik-Jan
- O'Sullivan, John D
- Korenke, G Christoph
- Bloem, Bastiaan R
- de Coo, Irenaeus F
- Verhagen, Judith M A
- Said, Ines
- Prescott, Trine
- Stray-Pedersen, Asbjørg
- Rasmussen, Magnhild
- Vears, Danya F
- Lehesjoki, Anna-Elina
- Corbett, Mark A
- Bahlo, Melanie
- Gecz, Jozef
- Dibbens, Leanne M
- Berkovic, Samuel F
Producer: 20130530
In:
Brain : a journal of neurology vol. 136
Availability: No items available.
|
|
|
20.
|
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. [electronic resource] by
- Carrozzo, Rosalba
- Verrigni, Daniela
- Rasmussen, Magnhild
- de Coo, Rene
- Amartino, Hernan
- Bianchi, Marzia
- Buhas, Daniela
- Mesli, Samir
- Naess, Karin
- Born, Alfred Peter
- Woldseth, Berit
- Prontera, Paolo
- Batbayli, Mustafa
- Ravn, Kirstine
- Joensen, Fróði
- Cordelli, Duccio M
- Santorelli, Filippo Maria
- Tulinius, Mar
- Darin, Niklas
- Duno, Morten
- Jouvencel, Philippe
- Burlina, Alberto
- Stangoni, Gabriela
- Bertini, Enrico
- Redonnet-Vernhet, Isabelle
- Wibrand, Flemming
- Dionisi-Vici, Carlo
- Uusimaa, Johanna
- Vieira, Paivi
- Osorio, Andrés Nascimento
- McFarland, Robert
- Taylor, Robert W
- Holme, Elisabeth
- Ostergaard, Elsebet
Producer: 20161213
In:
Journal of inherited metabolic disease vol. 39
Availability: No items available.
|