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Mårten Kyllerman

Reader

Mårten Kyllerman
Reader
marten.kyllerman@gu.se
+46 31-343 47 25

Postal Address: Rondvägen 10, 41685 Göteborg
Visiting Address: Rondvägen 10 , 41685 Göteborg


Department of Pediatrics at Institute of Clinical Sciences (More Information)
Drottning Silvias Barn O ungdomsjukh
416 85 Göteborg
Visiting Address: Drottning Silvias Barn O ungdomsjukh , 416 85 Göteborg

Latest publications

Bengt Hagberg.
Christopher Gillberg, I Carina Gillberg, Peder Rasmussen, Mårten Kyllerman, Elisabeth Fernell et al.
Acta paediatrica (Oslo, Norway : 1992), Magazine article 2015
Magazine article

In Memoriam: Bengt Arthur Hagberg, MD, PhD August 9, 1923-April 12, 2015.
Alan Percy, Mårten Kyllerman
Pediatric neurology, Magazine article 2015
Magazine article

Angelman syndrome.
Mårten Kyllerman
Handbook of clinical neurology, Journal article 2013
Journal article

Belly dancer syndrome.
Marta Coelho, Mårten Kyllerman
Acta Paediatrica, Journal article 2012
Journal article

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.
Andrea Poretti, Giuseppina Vitiello, Raoul C M Hennekam, Filippo Arrigoni, Enrico Bertini et al.
Orphanet journal of rare diseases, Journal article 2012
Journal article

Huvudvärk
Mårten Kyllerman
Barnmedicin, (red) K.Hanseus, H.Lagercrantz, T. Lindberg., Lund, Studentlitteratur, Chapter in book 2012
Chapter in book

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.
Yasmin Namavar, Peter G Barth, Paul R Kasher, Fred van Ruissen, Knut Brockmann et al.
Brain : a journal of neurology, Journal article 2011
Journal article

Showing 11 - 20 of 40

2011

Diagnosis and management of glutaric aciduria type I--revised recommendations.
Stefan Kölker, Ernst Christensen, James V Leonard, Cheryl R Greenberg, Avihu Boneh et al.
Journal of inherited metabolic disease, Journal article 2011
Journal article

2010

2009

SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration.
Hanna Orlén, Atle Melberg, Raili Raininko, Eva Kumlien, Miriam Entesarian et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics , Journal article 2009
Journal article

2008

Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations
Knut Brockmann, Steffi Dreha-Kulaczewski, Peter Dechent, Carsten Boennemann, Gunther Helms et al.
Journal of Neurology, Journal article 2008
Journal article

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
Gregor D. Gilfillan, Kaja K. Selmer, Ingrid Roxrud, Raffaella Smith, Mårten Kyllerman et al.
American Journal of Human Genetics, Journal article 2008
Journal article

2007

Aicardi Symdrome: Follow-Up Investigation of Swedish Children born in 1975-2002
L Palmér L, B Zetterlund, Anna-Lena Hård, Karin Sterneryd, Mårten Kyllerman
Neuropediatrics, Journal article 2007
Journal article

2006

Alexander disease - Ventricular garlands and abnormalities of the medulla and spinal cord
M.S. Van Der Knaap, V. Ramesh, R. Schiffmann, S. Blaser, Mårten Kyllerman et al.
NEUROLOGY, Journal article 2006
Journal article

Showing 11 - 20 of 40

Page Manager: Katarina Olinder Eriksson|Last update: 10/1/2013
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