Publications by authors named "Margareta Albage"

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Paediatric haematohidrosis: an overview of a rare but clinically distinct condition.
Karl Hansson, Emma K Johansson, Margareta Albåge, Natalia Ballardini

Acta Paediatr· June 2019

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A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9.
Emma Tham, Erik A Eklund, Anna Hammarsjö, Per Bengtson, Stefan Geiberger

Eur J Hum Genet· February 2016

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Novel alterations in the epigenetic signature of MeCP2-targeted promoters in lymphocytes of Rett syndrome patients.
Tobias Lilja, Karolina Wallenborg, Karin Björkman, Margareta Albåge, Maud Eriksson

Epigenetics· March 2013

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Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.
Saideh Rajaei, Anna Erlandson, Marten Kyllerman, Margareta Albage, Isa Lundstrom

J Child Neurol· January 2011

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Disturbances in cardiorespiratory function during day and night in Rett syndrome.
Malin Rohdin, Elisabeth Fernell, Maud Eriksson, Margareta Albåge, Hugo Lagercrantz

Pediatr Neurol· November 2007

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