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Acta Paediatrica (Oslo, Norway : 1992)|June 1, 1993
Early clinical symptoms and incidence of aspartylglucosaminuria in FinlandM Arvio, S Autio, P LouhialaClinical Genetics|November 1, 1988
Clinical features in a de novo interstitial deletion 15q13 to q15S Autio, H Pihko, C TengströmActa Neuropathologica|January 1, 1975
Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studiesM Haltia, J Palo, S AutioBirth Defects Original Article Series|January 1, 1974
Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritanceS Autio, J Palo, J PerheentupaAnnals of Clinical Research|April 1, 1982
The clinical course of mannosidosisS Autio, T Louhimo, M HeleniusEuropean Journal of Cardiology|March 1, 1978
Extracardiac malformations associated with congenital heart diseaseE I Wallgren, B Landtman, J RapolaJournal of Ocular Pharmacology|January 1, 1988
Timolol binding to bovine ocular melanin in vitroP Aula, T Kaila, R Huupponen, et al.Archives of Disease in Childhood|July 1, 1982
Long-term outcome of primary nephrotic syndromeO Koskimies, J Vilska, J Rapola, et al.Neuropediatrics|August 1, 1982
A variant of Jansky-Bielschowsky diseaseP Santavuori, J Rapola, K Sainio, et al.The Journal of Pediatrics|December 24, 1997
Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Palotie, et al.Pageof 27