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Application of a new monoclonal antibody for time-resolved fluoroimmunoassay of human pancreatic phospholipase A2

European journal of clinical chemistry and clinical biochemistry, 1991-12, Vol.29 (12), p.819

1991

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TOISENLAISIA NAISIA JA ENTISIÄ HETEROITA – vuoropuhelu seksuaalisen identiteetin kertomisen keinoista ja ongelmista

SQS, 2020-01, Vol.13 (1-2), p.80-87

2020

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Ibuprofen or acetaminophen for the acute treatment of migraine in children: a double-blind, randomized, placebo-controlled, crossover study

Neurology, 1997-01, Vol.48 (1), p.103-107

1997

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Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

Nature (London), 1995-08, Vol.376 (6541), p.584-587

1995

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Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

Neurology, 2001-04, Vol.56 (8), p.1059-1069

2001

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Psychiatric symptoms of children and adolescents with juvenile neuronal ceroid lipofuscinosis

Journal of intellectual disability research, 2005-01, Vol.49 (1), p.25-32

2005

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CLN5 , a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis

Nature genetics, 1998-07, Vol.19 (3), p.286-288

1998

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Rapid and simple assay for the determination of tripeptidyl peptidase and palmitoyl protein thioesterase activities in dried blood spots

Clinical chemistry (Baltimore, Md.), 2003-03, Vol.49 (3), p.509-511

2003

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Neuronal ceroid-lipofuscinoses in childhood

Brain & development (Tokyo. 1979), 1988, Vol.10 (2), p.80-83

Santavuori, Pirkko

1988

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Sumatriptan for migraine attacks in children: a randomized placebo-controlled study. Do children with migraine respond to oral sumatriptan differently from adults?

Neurology, 1997-04, Vol.48 (4), p.1100-1103

1997

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Phenotype-genotype correlation in eight patients with Finnish variant late infantile NCL (CLN5)

Neurology, 2000-08, Vol.55 (4), p.579-581

2000

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Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping

American journal of human genetics, 1999, Vol.64 (1), p.126-135

1999

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Epilepsy and Antiepileptic Drug Therapy in Juvenile Neuronal Ceroid Lipofuscinosis

Epilepsia (Copenhagen), 2000-10, Vol.41 (10), p.1296-1302

2000

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Muscle-eye-brain disease: A neuropathological study

Annals of neurology, 1997-02, Vol.41 (2), p.173-180

1997

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Clinical and magnetic resonance imaging findings in batten disease: Analysis of the major mutation (1.02-kb deletion)

Annals of neurology, 1997-11, Vol.42 (5), p.799-802

1997

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Neuronal ceroid lipofuscinoses in childhood

Neurological sciences, 2000-01, Vol.21 (3 Suppl), p.S35-S41

2000

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Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency

European journal of neurology, 2007-04, Vol.14 (4), p.369-372

2007

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Lamotrigine Therapy in Juvenile Neuronal Ceroid Lipofuscinosis

Epilepsia (Copenhagen), 1999-06, Vol.40 (6), p.796-799

1999

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Clinical and neuroradiological diagnostic aspects of neuronal ceroid lipofuscinoses disorders

European journal of paediatric neurology, 2001, Vol.5, p.157-161

2001

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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

Neuroradiology, 1997-05, Vol.39 (5), p.371-377

1997

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Oral dihydroergotamine for therapy-resistant migraine attacks in children

Pediatric neurology, 1997-02, Vol.16 (2), p.114-117

1997

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Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis

Neurology, 2001-10, Vol.57 (8), p.1411-1416

2001

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Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses

American journal of human genetics, 1994-10, Vol.55 (4), p.695-701

1994

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A Rapid Fluorogenic Palmitoyl-Protein Thioesterase Assay: Pre- and Postnatal Diagnosis of INCL

Molecular genetics and metabolism, 1999-04, Vol.66 (4), p.240-244

1999

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Decreased striatal dopamine transporter density in JNCL patients with parkinsonian symptoms

Neurology, 2000-03, Vol.54 (5), p.1069-1074

2000

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Application of a new monoclonal antibody for time-resolved fluoroimmunoassay of human pancreatic phospholipase A2

TOISENLAISIA NAISIA JA ENTISIÄ HETEROITA – vuoropuhelu seksuaalisen identiteetin kertomisen keinoista ja ongelmista

Ibuprofen or acetaminophen for the acute treatment of migraine in children: a double-blind, randomized, placebo-controlled, crossover study

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

Psychiatric symptoms of children and adolescents with juvenile neuronal ceroid lipofuscinosis

CLN5 , a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis

Rapid and simple assay for the determination of tripeptidyl peptidase and palmitoyl protein thioesterase activities in dried blood spots

Neuronal ceroid-lipofuscinoses in childhood

Sumatriptan for migraine attacks in children: a randomized placebo-controlled study. Do children with migraine respond to oral sumatriptan differently from adults?

Phenotype-genotype correlation in eight patients with Finnish variant late infantile NCL (CLN5)

Assignment of the Muscle-Eye-Brain Disease Gene to 1p32-p34 by Linkage Analysis and Homozygosity Mapping

Epilepsy and Antiepileptic Drug Therapy in Juvenile Neuronal Ceroid Lipofuscinosis

Muscle-eye-brain disease: A neuropathological study

Clinical and magnetic resonance imaging findings in batten disease: Analysis of the major mutation (1.02-kb deletion)

Neuronal ceroid lipofuscinoses in childhood

Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency

Lamotrigine Therapy in Juvenile Neuronal Ceroid Lipofuscinosis

Clinical and neuroradiological diagnostic aspects of neuronal ceroid lipofuscinoses disorders

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

Oral dihydroergotamine for therapy-resistant migraine attacks in children

Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis

Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses

A Rapid Fluorogenic Palmitoyl-Protein Thioesterase Assay: Pre- and Postnatal Diagnosis of INCL

Decreased striatal dopamine transporter density in JNCL patients with parkinsonian symptoms

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