Insight of autonomic dysfunction in CLN3 disease: a study on episodes resembling paroxysmal sympathetic hyperactivity (PSH) von Baekmann, C, Handrup, M M, Molgaard, H, Ejerskov, C, Jensen, H K, Ostergaard, J R

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Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing von Labrum, R W, Rajakulendran, S, Graves, T D, Eunson, L H, Bevan, R, Sweeney, M G, Hammans, S R, Tubridy, N, Britton, T, Carr, L J, Ostergaard, J R, Kennedy, C R, Al-Memar, A, Kullmann, D M, Schorge, S, Temple, K, Davis, M B, Hanna, M G

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Spinal manifestations of CLN1 disease start during the early postnatal period von Nelvagal, H. R., Dearborn, J. T., Ostergaard, J. R., Sands, M. S., Cooper, J. D.

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Cardiac involvement in juvenile neuronal ceroid lipofuscinosis (Batten disease) von ØSTERGAARD, J. R, RASMUSSEN, T. B, MØLGAARD, H

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Corrigendum to “Development of hypomelanotic macules is associated with constitutive activated mTORC1 in tuberous sclerosis complex” [Mol. Genet. Metab. 120(4) (Apr 2017) 384–391]... von Møller, L.B., Schönewolf-Greulich, B., Rosengren, T., Larsen, L.J., Ostergaard, J.R., Sommerlund, M., Ostenfeldt, C., Stausbøl-Grøn, B., Linnet, K.M., Gregersen, P.A., Jensen, U.B.

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Neuropsychology and brain morphology in Klinefelter syndrome – the impact of genetics von Skakkebæk, A., Bojesen, A., Kristensen, M. K., Cohen, A., Hougaard, D. M., Hertz, J. M., Fedder, J., Laurberg, P., Wallentin, M., Østergaard, J. R., Pedersen, A. D., Gravholt, C. H.

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Are cerebral aneurysms atherosclerotic ? von ADAMSON, J, HUMPHRIES, S. E, OSTERGAARD, J. R, VOLDBY, B, RICHARDS, P, POWELL, J. T

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PS-030 Congenital Heart Disease And Microcephaly At Birth: A Danish Population-based Cohort Study Of Children With Down Syndrome von Matthiesen, NB, Gaynor, JW, Henriksen, TB, Hjortdal, VE, Agergaard, P, Ostergaard, JR

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Recurrent Ophthalmoplegia in Childhood: Diagnostic and Etiologic Considerations von Østergaard, JR, Møller, HU, Christensen, T

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A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations von MUNOT, Pinki, SAUNDERS, Dawn E, JACQUES, Thomas S, COX, Timothy C, GANESAN, Vijeya, MILEWICZ, Dianna M, REGALADO, Ellen S, OSTERGAARD, John R, BRAUN, Kees P, KERR, Timothy, LICHTENBELT, Klaske D, PHILIP, Sunny, RITTEY, Christopher

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Smoking During Pregnancy and Hospitalization of the Child von Wisborg, Kirsten, Henriksen, Tine Brink, Obel, Carsten, Skajaa, Elisabet, Ostergaard, John R

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PS-030Congenital Heart Disease And Microcephaly At Birth: A Danish Population-based Cohort Study Of Children With Down Syndrome von Matthiesen, N B, Gaynor, J W, Henriksen, T B, Hjortdal, V E, Agergaard, P, Ostergaard, J R

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Developmental enamel defects in children prenatally exposed to anti-epileptic drugs von Jacobsen, Pernille E, Henriksen, Tine B, Haubek, Dorte, Ostergaard, John R

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Epilepsy and pregnancy: effect of antiepileptic drugs and lifestyle on birthweight von Hvas, Christian Lodberg, Henriksen, Tine Brink, østergaard, John R., Dam, Mogens

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A Distinct Difference in Clinical Expression of Two Siblings with Aicardi-Goutières Syndrome von Østergaard, J. R., Christensen, T., Nehen, Anne Marie

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Normal Cortisol Response to High-Dose Synacthen and Insulin Tolerance Test in Children and Adults with Prader-Willi Syndrome von Farholt, Stense, Sode-Carlsen, Rasmus, Christiansen, Jens Sandahl, Østergaard, John R, Høybye, Charlotte

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Efficacy of different antiepileptic drugs in children with Angelman syndrome associated with 15q11-13 deletion: the Danish experience von Østergaard, John R, Balslev, Thomas

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The Central Nervous System in Tay Syndrome von Østergaard, J. R., Christensen, T.

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PO-0416 2nd Trimester Head Size In Fetuses With Congenital Heart Disease: A Cohort Study von Lauridsen, MH, Petersen, OB, Vestergaard, EM, Henriksen, TB, Østergaard, JR, Matthiesen, NB, Hjortdal, VE

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Headache as a Warning Symptom of Impending Aneurysmal Subarachnoid Haemorrhage von OSTERGAARD, J. R

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