Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in Sweden von Thilen, Astrid, Nordenstrom, Anna, Hagenfeldt, Lars, von Dobeln, Ulrika, Guthenberg, Claes, Larsson, Agne

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Evolution of an influenza pandemic in 13 countries from 5 continents monitored by protein microarray from neonatal screening bloodspots von de Bruin, E, Loeber, J.G, Meijer, A, Castillo, G. Martinez, Cepeda, M.L. Granados, Torres-Sepúlveda, M. Rosario, Borrajo, G.J.C, Caggana, M, Giguere, Y, Meyer, M, Fukushi, M, Devi, A.R. Rama, Khneisser, I, Vilarinho, L, von Döbeln, U, Torresani, T, Mackenzie, J, Zutt, I, Schipper, M, Elvers, L.H, Koopmans, M.P.G

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Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast von Haglind, C. Bieneck, Nordenström, A., Ask, S., von Döbeln, U., Gustafsson, J., Stenlid, M. Halldin

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Identification of new mutations in the ETHE1 gene in a cohort of 14 patients presenting with ethylmalonic encephalopathy von Mineri, R, Rimoldi, M, Burlina, A B, Koskull, S, Perletti, C, Heese, B, von Döbeln, U, Mereghetti, P, Di Meo, I, Invernizzi, F, Zeviani, M, Uziel, G, Tiranti, V

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Measurement of ATP production and respiratory chain enzyme activities in mitochondria isolated from small muscle biopsy samples von Wibom, Rolf, Hagenfeldt, Lars, von Döbeln, Ulrika

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Erratum to: Increased and early lipolysis in children with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency during fast von Haglind, C. Bieneck, Nordenström, A., Ask, S., von Döbeln, U., Gustafsson, J., Stenlid, M. Halldin

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Carbohydrate-deficient transferrin in galactosaemia von Stibler, H., von Döbeln, U., Kristiansson, B., Guthenberg, C.

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Population Structure in Contemporary Sweden—A Y‐Chromosomal and Mitochondrial DNA Analysis von Lappalainen, T., Hannelius, U., Salmela, E., Von Döbeln, U., Lindgren, C. M., Huoponen, K., Savontaus, M.‐L., Kere, J., Lahermo, P.

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Neuropsychological Development in Patients with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency von Strandqvist, A., Haglind, C. Bieneck, Zetterström, R. H., Nemeth, A., von Döbeln, U., Stenlid, M. Halldin, Nordenström, A.

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Pregnancy and lactation in a woman with classical galactosaemia heterozygous for p.Q188R and p.R333W von Ohlsson, A., Nasiell, J., Döbeln, U.

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Increased neonatal thyrotropin in Down syndrome von Myrelid, Å, Jonsson, B, Guthenberg, C, Von Döbeln, U, Annerén, G, Gustafsson, J

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Fatty acid oxidation in fibroblasts from patients with defects in β‐oxidation and in the respiratory chain von Venizelos, N., Döbeln, U., Hagenfeldt, L.

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Increased lipolysis in LCHAD deficiency von Halldin, M. U., Forslund, A., Döbeln, U., Eklund, C., Gustafsson, J.

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Secondary metabolic effects in complex I deficiency von Esteitie, Nayla, Hinttala, Reetta, Wibom, Rolf, Nilsson, Helene, Hance, Nicole, Naess, Karin, Teär-Fahnehjelm, Kristina, Von Döbeln, Ulrika, Majamaa, Kari, Larsson, Nils-Göran

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Alterations of mitochondrial function and correlations with personality traits in selected major depressive disorder patients von Gardner, Ann, Johansson, Anna, Wibom, Rolf, Nennesmo, Inger, von Döbeln, Ulrika, Hagenfeldt, Lars, Hällström, Tore

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Clinical and biochemical presentation of long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency von Hagenfeldt, L., Venizelos, N., Döbeln, U.

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Serum amino acid profile in patients with acute pancreatitis von Sandstrom, P, Trulsson, L, Gasslander, T, Sundqvist, T, von Dobeln, U, Svanvik, J

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Placental transfer of maternally-derived IgA precludes the use of guthrie card eluates as a screening tool for primary immunodeficiency diseases von Borte, Stephan, Janzi, Magdalena, Pan-Hammarström, Qiang, von Döbeln, Ulrika, Nordvall, Lennart, Winiarski, Jacek, Fasth, Anders, Hammarström, Lennart

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Heat differentiated complement factor profiling von Hamsten, Carl, Skattum, Lillemor, Truedsson, Lennart, von Döbeln, Ulrika, Uhlén, Mathias, Schwenk, Jochen M., Hammarström, Lennart, Nilsson, Peter, Neiman, Maja

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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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