Psychiatric symptoms of children and adolescents with juvenile neuronal ceroid lipofuscinosis von Bäckman, M. L., Santavuori, P. R., Åberg, L. E., Aronen, E. T.

Volltext

Oral dihydroergotamine for therapy-resistant migraine attacks in children von Hämäläinen, Mirja L., Hoppu, Kalle, Santavuori, Pirkko R.

Volltext

Effect of age on the fulfilment of the IHS criteria for migraine in children at a headache clinic von HÄMÄLÄINEN, M. L, HOPPU, K, SANTAVUORI, P. R

Volltext

New antidepressive and antipsychotic drugs in juvenile neuronal ceroid lipofuscinoses — a pilot study von Bäckman, Maria L., berg, Laura E., Aronen, Eeva T., Santavuori, Pirkko R.

Volltext

Transdermal fentanyl therapy for pains in children with infantile neuronal ceroid lipofuscinosis von Mannerkoski, M K, Heiskala, H J, Santavuori, P R, Pouttu, J A

Volltext

Effect of Age on The Fulfilment of the IHS Criteria for Migraine in Children at a Headache Clinic von Hämäläinen, ML, Hoppu, K, Santavuori, PR

Volltext

Psychiatric symptoms of children and adolescents with juvenile neuronal ceroid lipofuscinosis: Mental Health and Intellectual Disability: XVI von BÄCKMAN, M. L, SANTAVUORI, P. R, ABERG, L. E, ARONEN, E. T

Volltext

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease von CORMAND, B, PIHKO, H, VOIT, T, TOPALOGLU, H, DOBYNS, W. B, LEHESJOKI, A.-E, BAYES, M, VALANNE, L, SANTAVUORI, P, TALIM, B, GERSHONI-BARUCH, R, AHMAD, A, VAN BOKHOVEN, H, BRUNNER, H. G

Volltext

Rapid and simple assay for the determination of tripeptidyl peptidase and palmitoyl protein thioesterase activities in dried blood spots von Lukacs, Zoltan, Santavuori, Pirkko, Keil, Angelika, Steinfeld, Robert, Kohlschütter, Alfried

Volltext

Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency von Kälviäinen, R., Eriksson, K., Losekoot, M., Sorri, I., Harvima, I., Santavuori, P., Järvelä, I., Autti, T., Vanninen, R., Salmenperä, T., Van Diggelen, O. P.

Volltext

Clinical and magnetic resonance imaging findings in batten disease: Analysis of the major mutation (1.02-kb deletion) von Järvelä, Irma, Autti, Taina, Lamminranta, Sirkka, Åberg, Laura, Raininko, Raili, Santavuori, Pirkko

Volltext

MRI of neuronal ceroid lipofuscinosis. II. Postmortem MRI and histopathological study of the brain in 16 cases of neuronal ceroid lipofuscinosis of juvenile or late infantile type von AUTTI, T, RAININKO, R, SANTAVUORI, P, VANHANEN, S. L, POUTANEN, V. P, HALTIA, M

Volltext

Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses von SAVUKOSKI, M, KESTILÄ, M, WILLIAMS, R, JÄRVELÄ, I, SHARP, J, HARRIS, J, SANTAVUORI, P, GARDINER, M, PELTONEN, L

Volltext

CSF insulin-like growth factor-1 in infantile neuronal ceroid lipofuscinosis von RIIKONEN, R, VANHANEN, S.-L, TYYNELÄ, J, SANTAVUORI, P, TURPEINEN, U

Volltext

Neuroradiological Findings (MRS, MRI, SPECT) in Infantile Neuronal Ceroid-Lipofuscinosis (Infantile CLN1) at Different Stages of the Disease von Vanhanen, S.-L., Puranen, J., Autti, T., Raininko, R., Liewendahl, K., Nikkinen, P., Santavuori, P., Suominen, P., Vuori, K., Häkkinen, A.-M.

Volltext

Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis von LAURONEN, L, MUNROE, P. B, KIRVESKARI, E, SANTAVUORI, P, JÄRVELÄ, I, AUTTI, T, MITCHISON, H. M, O'RAWE, A. M, GARDINER, R. M, MOLE, S. E, PURANEN, J, HÄKKINEN, A.-M

Volltext

The age of human mutation : Genealogical and linkage disequilibrium analysis of the CLN5 mutation in the finnish population von VARILO, T, SAVUKOSKI, M, NORIO, R, SANTAVUORI, P, PELTONEN, L, JÄRVELÄ, I

Volltext

MRI of neuronal ceroid lipofuscinosis : I. Cranial MRI of 30 patients with juvenile neuronal ceroid lipofuscinosis von AUTTI, T, RAININKO, R, VANHANEN, S. L, SANTAVUORI, P

Volltext

Hereditary and Acquired Risk Factors for Childhood Stroke von Riikonen, R., Santavuori, P.

Volltext

Neuropsychological test battery in the follow-up of patients with juvenile neuronal ceroid lipofuscinosis von LAMMINRANTA, S, ABERG, L. E, AUTTI, T, MOREN, R, LAINE, T, KAUKORANTA, J, SANTAVUORI, P

Volltext