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Orphanet Journal of Rare Diseases|December 2, 2016
Aspartylglycosaminuria: a reviewMaria Arvio, Ilkka MononenTherapeutic Drug Monitoring|July 27, 2002
Serious neutropenia in ALL patients treated with L-asparaginase may be avoided by therapeutic monitoring of the enzyme activity in the circulationPäivi Ylikangas, Ilkka MononenGlycobiology|September 3, 2004
Massive accumulation of Man2GlcNAc2-Asn in nonneuronal tissues of glycosylasparaginase-deficient mice and its removal by enzyme replacement therapyEira Kelo, Ulla Dunder, Ilkka MononenAmerican 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 LähdetieAmerican 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 LähdetieJournal 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-LaaksoActa 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 PöntinenFEBS 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.Pageof 4