Inverse medium problem for a singular contrast von Serov, V., Tyni, T.

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Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy von Auranen, M, MD PhD, Paetau, A, MD PhD, Piirilä, P, MD PhD, Pohju, A, RD MSc, Salmi, T, MD PhD, Lamminen, A, MD PhD, Löfberg, M, MD PhD, Mosegaard, S, MSc, Olsen, RK, MSc PhD, Tyni, T, MD PhD

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Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency von Tyni, Tiina, Ekholm, Eeva, Pihko, Helena

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Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase 1 deficiency von ROOMETS, E, LUNDBOM, N, PIHKO, H, HEIKKINEN, S, TYNI, T

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Mitochondrial Fatty Acid beta-Oxidation in the Retinal Pigment Epithelium von TYNI, T.

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Moyamoya angiopathy: radiological follow-up findings in Finnish patients von Savolainen, Marika, Pekkola, Johanna, Mustanoja, Satu, Tyni, Tiina, Hernesniemi, Juha, Kivipelto, Leena, Tatlisumak, Turgut

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Long-chain 3-hydroxyacyl–coenzyme A dehydrogenase deficiency with the G1528C mutation: Clinical presentation of thirteen patients von Tyni, Tiina, Palotie, Aarno, Viinikka, Lasse, Valanne, Leena, Salo, Matti K., von Döbeln, Ulrika, Jackson, Sandra, Wanders, Ronald, Venizelos, Nikolaos, Pihko, Helena

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Moyamoya angiopathy: long-term follow-up study in a Finnish population von Savolainen, Marika, Mustanoja, Satu, Pekkola, Johanna, Tyni, Tiina, Uusitalo, Anna-Maria, Ruotsalainen, Sanni, Poutiainen, Erja, Hernesniemi, Juha, Kivipelto, Leena, Tatlisumak, Turgut

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MLP032 LCHAD deficiency: follow-up of patients with pigmentary retinopathy von Tyni, T, Immonen, T, Lindahl, P, Kivelä, T

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Evolutionary bi-objective optimisation in the elevator car routing problem von Tyni, Tapio, Ylinen, Jari

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Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutation von Tyni, Tiina, Rapola, Juhani, Palotie, Aarno, Pihko, Helena

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Early dietary therapy in preventing progression of retinopathy in long‐chain 3‐hydroxyacyl‐CoA dehydrogenase (LCHAD) deficiency caused by the homozygous G1528C mutation von ROOMETS, E, KIVELÄ, T, TYNI, T

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Morphological and molecular identification of the freshwater crab, Barytelphusa cunicularis from Kanniyakumari, India von Raj, T G Teeni Janet, Suganthi, A Shyla, Raj, T G Tyni Joice, Anilkumar, G

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Mitochondrial fatty acid β-oxidation in the human eye and brain: Implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency von TYNI, Tiina, PAETAU, Anders, STRAUSS, Arnold W, MIDDLETON, Bruce, KIVELÄ, Tero

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Morphological and molecular identification of the freshwater crab, Barytelphusa cunicularis from Kanniyakumari, India von Teeni Janet Raj, T.G., Shyla Suganthi, A., Tyni Joice Raj, T.G., Anilkumar, G.

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Serious pregnancy complications in a patient with previously undiagnosed carnitine palmitoyltransferase 1 deficiency von Ylitalo, Kati, Vänttinen, Tuomo, Halmesmäki, Erja, Tyni, Tiina

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Expanding screening for rare metabolic disease in the newborn : An analysis of costs, effect and ethical consequences for decision-making in Finland von AUTTI-RÄMÖ, Ilona, MÄKELÄ, Marjukka, RENLUND, Martin, SALO, Matti, TYNI, Tiina, SINTONEN, Harri, KOSKINEN, Hanna, LAAJALAHTI, Liisa, HALILA, Ritva, KÄÄRIÄINEN, Helena, LAPATTO, Risto, NÄNTÖ-SALONEN, Kirsti, PULKXI, Kari

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Evolutionary Bi-objective Controlled Elevator Group Regulates Passenger Service Level and Minimises Energy Consumption von Tyni, Tapio, Ylinen, Jari

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Ophthalmologic findings in long-chain 3-hydroxyacyl-Coa dehydrogenase deficiency caused by the G1528C mutation: A new type of hereditary metabolic chorioretinopathy von Tyni, Tiina, Kivelä, Tero, Lappi, Marjatta, Summanen, Paula, Nikoskelainen, Eeva, Pihko, Helena

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Analysis of mitochondrial fatty acid oxidation intermediates by tandem mass spectrometry from intact mitochondria prepared from homogenates of cultured fibroblasts, skeletal muscle... von TYNI, Tiina, POURFARZAM, Morteza, TURNBULL, Douglass M

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