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Kyllerman, Mårten
46
results:
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Online (46)
Mediatypes
Articles (Online) (41)
OpenAccess-fulltext (5)
Sorted by: Relevance
Sorted by: Year
?
1
Bengt Hagberg (1923-2015), Swedish father of child neurolog:
Kyllerman, Mårten
Acta Paediatrica. 105 (2016) 12 - p. 1405-1407 , 2016
Link:
https://doi.org/10.1111/..
?
2
In Memoriam: Bengt Arthur Hagberg, MD, PhD—August 9, 1923–A..:
Percy, Alan
;
Kyllerman, Mårten
Journal of Child Neurology. 32 (2016) 2 - p. 252-254 , 2016
Link:
https://doi.org/10.1177/..
?
3
In Memoriam: Bengt Arthur Hagberg, MD, PhD August 9, 1923-A..:
Percy, Alan
;
Kyllerman, Mårten
Pediatric Neurology. 53 (2015) 2 - p. 105-107 , 2015
Link:
https://doi.org/10.1016/..
?
4
Bengt Hagberg:
Gillberg, Christopher
;
Gillberg, Carina
;
Rasmussen, Peder
...
Acta Paediatrica. 104 (2015) 10 - p. 1064-1064 , 2015
Link:
https://doi.org/10.1111/..
?
5
Old and New Entities with Rett or Angelman‐Like Intellectua..:
Kyllerman, Mårten
Acta Paediatrica. 101 (2012) 10 - p. 1099-1099 , 2012
Link:
https://doi.org/10.1111/..
?
6
Delineation and Diagnostic Criteria of Oral-Facial-Digital ..:
Poretti, Andrea
;
Vitiello, Giuseppina
;
Hennekam, Raoul CM
...
Orphanet Journal of Rare Diseases. 7 (2012) 1 - p. , 2012
Link:
https://doi.org/10.1186/..
?
7
Aetiology of severe mental retardation and further genetic ..:
Lundvall, Mikael
;
Rajaei, Saideh
;
Erlandson, Anna
.
Acta Paediatrica. 101 (2011) 1 - p. 85-91 , 2011
Link:
https://doi.org/10.1111/..
?
8
Diagnosis and management of glutaric aciduria type I – revi..:
Kölker, Stefan
;
Christensen, Ernst
;
Leonard, James V.
...
Journal of Inherited Metabolic Disease. 34 (2011) 3 - p. 677-694 , 2011
Link:
https://doi.org/10.1007/..
?
9
Early Infantile Onset ''Congenital'' Rett Syndrome Variants..:
Rajaei, Saideh
;
Erlandson, Anna
;
Kyllerman, Marten
...
Journal of Child Neurology. 26 (2011) 1 - p. 65-71 , 2011
Link:
https://doi.org/10.1177/..
?
10
Speech, language, and cognitive dysfunction in children wit..:
Rejnö-Habte Selassie, Gunilla
;
Hedström, Anders
;
Viggedal, Gerd
..
Epilepsy & Behavior. 18 (2010) 3 - p. 267-275 , 2010
Link:
https://doi.org/10.1016/..
?
11
SPG11mutations cause Kjellin syndrome, a hereditary spastic..:
Örlén, Hanna
;
Melberg, Atle
;
Raininko, Raili
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 150B (2009) 7 - p. 984-992 , 2009
Link:
https://doi.org/10.1002/..
?
12
Juvenile galactosialidosis with attacks of neuropathic pain..:
Darin, Niklas
;
Kyllerman, Mårten
;
Hård, Anna-Lena
..
European Journal of Paediatric Neurology. 13 (2009) 6 - p. 553-555 , 2009
Link:
https://doi.org/10.1016/..
?
13
tRNA splicing endonuclease mutations cause pontocerebellar ..:
Budde, Birgit S
;
Namavar, Yasmin
;
Barth, Peter G
...
Nature Genetics. 40 (2008) 9 - p. 1113-1118 , 2008
Link:
https://doi.org/10.1038/..
?
14
Cerebral involvement in axonal Charcot-Marie-Tooth neuropat..:
Brockmann, Knut
;
Dreha-Kulaczewski, Steffi
;
Dechent, Peter
...
Journal of Neurology. 255 (2008) 7 - p. , 2008
Link:
https://doi.org/10.1007/..
?
15
Beckung and Kyllerman reply:
Beckung, Eva
;
Kyllerman, Mårten
Developmental Medicine & Child Neurology. 47 (2005) 2 - p. 143-143 , 2005
Link:
https://doi.org/10.1017/..
1-15