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	1.	Angelman syndrome. [electronic resource] by Kyllerman, Mårten Producer: 20140401 In: Handbook of clinical neurology vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Bengt Hagberg (1923-2015), Swedish father of child neurology. [electronic resource] by Kyllerman, Mårten Producer: 20170328 In: Acta paediatrica (Oslo, Norway : 1992) vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	In Memoriam: Bengt Arthur Hagberg, MD, PhD August 9, 1923-April 12, 2015. [electronic resource] by Percy, Alan Kyllerman, Mårten Producer: 20160422 In: Pediatric neurology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Motor impairments, neurological signs, and developmental level in individuals with Angelman syndrome. [electronic resource] by Beckung, Eva Steffenburg, Suzanne Kyllerman, Mårten Producer: 20040503 In: Developmental medicine and child neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Odd MECP2-mutated Rett variant-long-term follow-up profile to age 25. [electronic resource] by Hagberg, Bengt Erlandsson, Anna Kyllerman, Mårten Larsson, Gunillla Producer: 20040203 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Aetiology of severe mental retardation and further genetic analysis by high-resolution microarray in a population-based series of 6- to 17-year-old children. [electronic resource] by Lundvall, Mikael Rajaei, Saideh Erlandson, Anna Kyllerman, Mårten Producer: 20120302 In: Acta paediatrica (Oslo, Norway : 1992) vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Pain, balance, activity, and participation in children with hypermobility syndrome. [electronic resource] by Schubert-Hjalmarsson, Elke Öhman, Anna Kyllerman, Mårten Beckung, Eva Producer: 20130206 In: Pediatric physical therapy : the official publication of the Section on Pediatrics of the American Physical Therapy Association vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Induced shift in myosin heavy chain expression in myosin myopathy by endurance training. [electronic resource] by Tajsharghi, Homa Sunnerhagen, Katharina Stibrant Darin, Niklas Kyllerman, Mårten Oldfors, Anders Producer: 20040525 In: Journal of neurology vol. 251 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Juvenile galactosialidosis with attacks of neuropathic pain and absence of sialyloligosacchariduria. [electronic resource] by Darin, Niklas Kyllerman, Mårten Hård, Anna-Lena Nordborg, Claes Månsson, Jan-Eric Producer: 20100114 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Comorbidity in severe developmental language disorders: neuropediatric and psychological considerations. [electronic resource] by Selassie, Gunilla Rejnö-Habte Jennische, Mårgareta Kyllerman, Mårten Viggedal, Gerd Hartelius, Lena Producer: 20050826 In: Acta paediatrica (Oslo, Norway : 1992) vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patients. [electronic resource] by Erlandson, Anna Samuelsson, Lena Hagberg, Bengt Kyllerman, Mårten Vujic, Mihailo Wahlström, Jan Producer: 20041021 In: Genetic testing vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Speech, language, and cognitive dysfunction in children with focal epileptiform activity: A follow-up study. [electronic resource] by Rejnö-Habte Selassie, Gunilla Hedström, Anders Viggedal, Gerd Jennische, Margareta Kyllerman, Mårten Producer: 20101020 In: Epilepsy & behavior : E&B vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2). [electronic resource] by Tajsharghi, Homa Darin, Niklas Rekabdar, Elham Kyllerman, Mårten Wahlström, Jan Martinsson, Tommy Oldfors, Anders Producer: 20050816 In: European journal of human genetics : EJHG vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis. [electronic resource] by Rajaei, Saideh Erlandson, Anna Kyllerman, Marten Albage, Margareta Lundstrom, Isa Karrstedt, Ewa-Lotta Hagberg, Bengt Producer: 20110525 In: Journal of child neurology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Subtelomeric rearrangements detected in patients with idiopathic mental retardation. [electronic resource] by Anderlid, Britt-Marie Schoumans, Jacqueline Annerén, Göran Sahlén, Sigrid Kyllerman, Mårten Vujic, Mihailo Hagberg, Bengt Blennow, Elisabeth Nordenskjöld, Magnus Producer: 20020626 In: American journal of medical genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Long-term follow-up, neurological outcome and survival rate in 28 Nordic patients with glutaric aciduria type 1. [electronic resource] by Kyllerman, Mårten Skjeldal, Ola Christensen, Ernst Hagberg, Gudrun Holme, Elisabeth Lönnquist, Tuula Skov, Liselotte Rotwelt, Terje von Döbeln, Ulrika Producer: 20040928 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations. [electronic resource] by Brockmann, Knut Dreha-Kulaczewski, Steffi Dechent, Peter Bönnemann, Carsten Helms, Gunther Kyllerman, Marten Brück, Wolfgang Frahm, Jens Huehne, Kathrin Gärtner, Jutta Rautenstrauss, Bernd Producer: 20081212 In: Journal of neurology vol. 255 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Bengt Hagberg. [electronic resource] by Gillberg, Christopher Gillberg, Carina Rasmussen, Peder Kyllerman, Mårten Fernell, Elisabeth Olsson, Ingrid Uvebrant, Paul Westerberg, Barbro Tulinius, Mar Himmelmann, Kate Bax, Martin Neville, Brian Producer: 20160629 In: Acta paediatrica (Oslo, Norway : 1992) vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration. [electronic resource] by Orlén, Hanna Melberg, Atle Raininko, Raili Kumlien, Eva Entesarian, Miriam Söderberg, Per Påhlman, Magnus Darin, Niklas Kyllerman, Mårten Holmberg, Eva Engler, Henry Eriksson, Urban Dahl, Niklas Producer: 20091228 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 150B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Pontine tegmental cap dysplasia: a novel brain malformation with a defect in axonal guidance. [electronic resource] by Barth, Peter G Majoie, Charles B Caan, Matthan W A Weterman, Marian A J Kyllerman, Marten Smit, Leo M E Kaplan, Richard A Haas, Richard H Baas, Frank Cobben, Jan-Maarten Poll-The, Bwee Tien Producer: 20071101 In: Brain : a journal of neurology vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 24 results.