Growth charts for monitoring postnatal growth at NICU of extreme preterm-born infants von Horemuzova, E, Söder, O, Hagenäs, L

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Retarded head growth and neurocognitive development in infants of mothers with a history of eating disorders: longitudinal cohort study von Koubaa, S, Hällström, T, Hagenäs, L, Hirschberg, AL

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SLC26A2 disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED) von Mäkitie, O., Geiberger, S., Horemuzova, E., Hagenäs, L., Moström, E., Nordenskjöld, M., Grigelioniene, G., Nordgren, A.

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Dose-Dependent Effect of Growth Hormone on Final Height in Children with Short Stature without Growth Hormone Deficiency von Albertsson-Wikland, Kerstin, Aronson, A. Stefan, Gustafsson, Jan, Hagenäs, Lars, Ivarsson, Sten A., Jonsson, Björn, Kriström, Berit, Marcus, Claude, Nilsson, Karl Olof, Ritzén, E. Martin, Tuvemo, Torsten, Westphal, Otto, Åman, Jan

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Placental IGF-I, Estrogen Receptor, and Progesterone Receptor Expression, and Maternal Anthropometry in Growth-Restricted Pregnancies in the Swedish Population von Akram, S.K., Sahlin, L., Östlund, E., Hagenäs, L., Fried, G., Söder, O.

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Plasma Leptin in Infants: Relations to Birth Weight and Weight Loss von Marchini, Giovanna, Fried, Gabriel, Ostlund, Eva, Hagenas, Lars

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Growth hormone treatment of children with Prader-Willi syndrome affects linear growth and body composition favourably von Lindgren, AC, Hagenas, L, Muller, J, Blichfeldt, S, Rosenborg, M, Brismar, T, Ritzen, EM

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OR11-6 Long-term mortality in patients with isolated GHD, ISS, and SGA treated with recombinant GH during childhood in Sweden: Application of a mortality model developed from the g... von Wikland, K. Albertsson, Sävendahl, L, Märtensson, A, Borgström, B, Niklasson, A, Pehrson, N.G, Bang, P, Dahlgren, J, Gustafson, J, Hagenäs, L, Kriström, B, Norgren, S, Odén, A

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Skeletal Dysplasia, Growth Hormone Treatment and Body Proportion: Comparison with Other Syndromic and Non-Syndromic Short Children von Hagenäs, Lars, Hertel, Thomas

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Insulin-like growth factor I in fetal serum obtained by cordocentesis is correlated with intrauterine growth retardation von Ostlund, E, Bang, P, Hagenäs, L, Fried, G

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Growth hormone treatment of short children born small-for-gestational-age: the Nordic Multicentre Trial von Boguszewski, M, Albertsson-Wikland, K, Aronsson, S, Gustafsson, J, Hagenas, L, Westgren, U, Westphal, O, Lipsanen-Nyman, M, Sipila, I, Gellert, P, Muller, J, Madsen, B

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Prevalence of coeliac disease in Turner syndrome von IVARSSON, S.-A, CARLSSON, A, MOËLL, C, NILSSON, K. O, TUVEMO, T, WESTPHAL, O, ALBERTSSON-WIKLAND, K, AMAN, J, BREDBERG, A, ALM, J, ARONSSON, S, GUSTAFSSON, J, HAGENÄS, L, HÄGER, A, KRISTRÖM, B, MARCUS, C

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Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity von GRIGELIONIENE, Giedre, SCHOUMANS, Jacqueline, NILSSON, Nils Östen, ELFVING, Maria, ELLIS, Ian, ANDERLID, Britt-Marie, FRANSSON, Ingegerd, TAPIA-PAEZ, Isabel, NORDENSKJÖLD, Magnus, HAGENÄS, Lars, DUMANSKI, Jan P, NEUMEYER, Lo, IVARSSON, Sten Anders, EKLÖF, Ole, ENKVIST, Ove, TORDAI, Paul, FOSDAL, Inger, MYHRE, Anne Grethe, WESTPHAL, Otto

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Metacarpophalangeal Pattern Profile Analysis in Leri-Weill Dyschondrosteosis von Laurencikas, E., Söderman, E., Grigelioniene, G., Hagenäs, L., Jorulf, H.

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Clinical charts for surveillance of growth and body proportion development in achondroplasia and examples of their use von Neumeyer, Luitgard, Merker, Andrea, Hagenäs, Lars

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Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia von GRIGELIONIENE, Giedre, EKLÖF, Ole, IVARSSON, Sten Anders, WESTPHAL, Otto, NEUMEYER, Lo, KEDRA, Darek, DUMANSKI, Jan, HAGENÄS, Lars

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Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort von Merker, Andrea, Neumeyer, Luitgard, Hertel, Niels Thomas, Grigelioniene, Giedre, Mäkitie, Outi, Mohnike, Klaus, Hagenäs, Lars

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Asn540Lys mutation in fibroblast growth factor receptor 3 and phenotype in hypochondroplasia von Grigelioniené, G, Eklöf, O, Laurencikas, E, Ollars, B, Hertel, NT, Dumanski, JP, Hagenäs, L

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The role of luteinizing hormone-β gene polymorphism in the onset and progression of puberty in healthy boys von RAIVIO, T, HUHTANIEMI, I, ANTTILA, R, SIIMES, M. A, HAGENÄS, L, NILSSON, C, PETTERSSON, K, DUNKEL, L

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Improved final height in girls with Turner's syndrome treated with growth hormone and oxandrolone von Nilsson, K O, Albertsson-Wikland, K, Alm, J, Aronson, S, Gustafsson, J, Hagenäs, L, Häger, A, Ivarsson, S A, Karlberg, J, Kriström, B, Marcus, C, Moell, C, Ritzen, M, Tuvemo, T, Wattsgård, C, Westgren, U, Westphal, O, Aman, J

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