Analysis of short stature homeobox-containing gene (SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity
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
Published in Human genetics (01.11.2001)
Published in Human genetics (01.11.2001)
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Growth hormone treatment in 35 prepubertal children with achondroplasia : A five-year dose-response trial
HERTEL, Niels Thomas, EKLÖF, Ole, MOHNIKE, Klaus, NEUMEYER, Lo, RITZEN, Martin, HAGENAS, Lars, IVARSSON, Sten, ARONSON, Stefan, WESTPHAL, Otto, SIPILÄ, Ilkka, KAITILA, Ilkka, BLAND, Jon, VEIMO, Dag, MÜLLER, Jørn
Published in Acta pædiatrica (Oslo) (01.10.2005)
Published in Acta pædiatrica (Oslo) (01.10.2005)
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Growth Hormone Treatment in Achondroplasia: 2 Year Results of a Dose-Response Study
Hagenäs, Lars, Aagenaes, Øystein, Eklöf, Ole, Hertel, Thomas, Kaitila, Ilkka, Mohnike, Klaus, Perhentuupa, Jaako, Ritzén, Martin, Sipilä, Ilkka, Müller, Jørn
Published in Clinical Pediatric Endocrinology (1997)
Published in Clinical Pediatric Endocrinology (1997)
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Mutations in short stature homeobox containing gene (SHOX) in dyschondrosteosis but not in hypochondroplasia
GRIGELIONIENE, Giedre, EKLÖF, Ole, IVARSSON, Sten Anders, WESTPHAL, Otto, NEUMEYER, Lo, KEDRA, Darek, DUMANSKI, Jan, HAGENÄS, Lars
Published in Human genetics (01.08.2000)
Published in Human genetics (01.08.2000)
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Growth hormone treatment in 35 prepubertal children with achondroplasia: A five-year dose-response trial
Thomas Hertel, Niels, Eklöf, Ole, Ivarsson, Sten, Aronson, Stefan, Westphal, Otto, Sipilä, Ilkka, Kaitila, Ilkka, Bland, Jon, Veimo, Dag, Müller, Jørn, Mohnike, Klaus, Neumeyer, Lo, Ritzen, Martin, Hagenäs, Lars
Published in Acta Paediatrica (01.10.2005)
Published in Acta Paediatrica (01.10.2005)
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A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome
Tentler, Dmitry, Gustavsson, Peter, Elinder, Göran, Eklöf, Ole, Gordon, Laurie, Mandel, Ariane, Dahl, Niklas
Published in Journal of medical genetics (01.02.2000)
Published in Journal of medical genetics (01.02.2000)
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Development of hypertension and uraemia after pyelonephritis in childhood: 27 year follow up
Jacobson, S. H., Eklöf, O., Eriksson, C. G., Lins, L. E., Tidgren, B., Winberg, J.
Published in BMJ (16.09.1989)
Published in BMJ (16.09.1989)
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