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Journal of Learning Disabilities|October 21, 2004
The Swedish WAIS-R factor structure and cognitive profiles for adults with dyslexiaJan Alm, Alan S KaufmanJournal of Inherited Metabolic Disease|February 13, 2010
Fructose 1,6-bisphosphatase deficiency: enzyme and mutation analysis performed on calcitriol-stimulated monocytes with a note on long-term prognosisCristine Åsberg, Ola Hjalmarson, Jan Alm, et al.Lakartidningen|April 19, 2002
[Cooperation reduces the risks of thyroid disease in pregnancy. Also mild maternal hypothyroidism can threaten the neurological development of the fetus]Annika Janson, Jan Alm, Katarina Bremme, et al.Nordic Journal of Psychiatry|April 5, 2008
The Adolescent Adjustment Profile (AAP) in comparisons of patients with obesity, phenylketonuria or neurobehavioural disordersGunilla Maria Olsson, Staffan Mårild, Jan Alm, et al.Acta Ophthalmologica|December 29, 2007
Ocular characteristics in 10 children with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: a cross-sectional study with long-term follow-upKristina Teär Fahnehjelm, Gerd Holmström, Liu Ying, et al.JIMD Reports|March 31, 2015
The Kuvan(®) Adult Maternal Paediatric European Registry (KAMPER) Multinational Observational Study: Baseline and 1-Year Data in Phenylketonuria Patients Responsive to SapropterinFriedrich K Trefz, Ania C Muntau, Florian B Lagler, et al.Hormone Research|November 23, 2006
Rapid genetic analysis in congenital hyperinsulinismHenrik B T Christesen, Klaus Brusgaard, Jan Alm, et al.European Journal of Endocrinology|May 3, 2008
Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutationHenrik B T Christesen, Nicholas D Tribble, Anders Molven, et al.Pageof 1