Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|May 6, 1999
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyT Tyni, H Pihko
Current Eye Research|July 15, 1998
Ophthalmic pathology in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutationT Tyni, H Pihko, T Kivelä
American Journal of Obstetrics and Gynecology|April 16, 1998
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyT Tyni, E Ekholm, H Pihko
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.
Neuromuscular Disorders : NMD|October 1, 1996
Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutationT Tyni, A Majander, H Kalimo, et al.
Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|May 1, 1997
Pathology of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutationT Tyni, J Rapola, A Paetau, et al.
Ophthalmology|May 21, 1998
Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathyT Tyni, T Kivelä, M Lappi, et al.
The Journal of Pediatrics|November 1, 1993
Transient ischemic cerebral lesions during induction chemotherapy for acute lymphoblastic leukemiaH Pihko, T Tyni, K Virkola, et al.
Neuromuscular Disorders : NMD|April 24, 2017
Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapyM Auranen, A Paetau, P Piirilä, et al.
The Journal of Pediatrics|January 1, 1997
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patientsT Tyni, A Palotie, L Viinikka, et al.
Pageof 1