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Orphanet Journal of Rare Diseases|December 2, 2016
Aspartylglycosaminuria: a reviewMaria Arvio, Ilkka Mononen
American Journal of Medical Genetics. Part A|November 17, 2020
Adult phenotype of the homozygous missense mutation c.655G>A, p.Gly219Arg in SLC13A5: A case reportMaria Arvio, Jaana Lähdetie
American Journal of Medical Genetics. Part A|May 4, 2021
Natural history of alpha-thalassemia X-linked intellectual disability syndrome: A case report of a 45-year-old manMaria Arvio, Jaana Lähdetie
Journal of Inherited Metabolic Disease|July 8, 2010
Early initiation of enzyme replacement therapy improves metabolic correction in the brain tissue of aspartylglycosaminuria miceUlla Dunder, Pirjo Valtonen, Eira Kelo, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|May 1, 2021
Screening of dementia indicating signs in adults with intellectual disabilitiesMaria Arvio, Nina Bjelogrlic-Laakso
Acta Paediatrica (Oslo, Norway : 1992)|December 9, 2015
Discrepancies between plasma procalcitonin and C-reactive protein levels are common in acute illnessLauri Ivaska, Varpu Elenius, Ilkka Mononen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|July 6, 2010
[Modified Atkins diet brought back the joy of life to a developmentally severely disabled youth]Maria Arvio, Liisa Kuisma, Mervi Pöntinen
FEBS Letters|September 26, 2002
Beta-aspartylpeptides as substrates of L-asparaginases from Escherichia coli and Erwinia chrysanthemiEira Kelo, Tiina Noronkoski, Ivanka B Stoineva, et al.
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