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Neurology
|
May 22, 1998
Bright light suppresses melatonin in blind patients with neuronal ceroid-lipofuscinoses
T Hätönen, M L Laakso, H Heiskala, et al.
Acta Radiologica (Stockholm, Sweden : 1987)
|
March 10, 2009
Brain magnetic resonance imaging of siblings from families with two or more children with learning or intellectual disabilities and need for full-time special education
M Mannerkoski, H Heiskala, R Raininko, et al.
Brain & Development
|
November 1, 1996
West syndrome: individualized ACTH therapy
H Heiskala, R Riikonen, P Santavuori, et al.
American Journal of Medical Genetics
|
December 18, 2001
Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?
P Nokelainen, H Heiskala, R Raininko, et al.
Journal of Sleep Research
|
March 21, 2002
Neurological impairments and sleep-wake behaviour among the mentally retarded
N Lindblom, H Heiskala, M Kaski, et al.
Neuropediatrics
|
February 1, 1997
Brain perfusion SPECT abnormalities in neuronal ceroid lipofuscinoses
K Liewendahl, S L Vanhanen, H Heiskala, et al.
Neuropediatrics
|
February 1, 1997
Lamotrigine therapy in infantile neuronal ceroid lipofuscinosis (INCL)
L Aberg, H Heiskala, S L Vanhanen, et al.
Neuroreport
|
April 11, 2000
No evidence for extraocular light induced phase shifting of human melatonin, cortisol and thyrotropin rhythms
N Lindblom, H Heiskala, T Hätönen, et al.
American Journal of Medical Genetics
|
June 5, 1995
Circadian rhythm studies in neuronal ceroid-lipofuscinosis (NCL)
E Heikkilä, T H Hàtònen, T Telakivi, et al.
Annals of Neurology
|
June 9, 1999
Extensive cerebral white matter abnormality without clinical symptoms: a new hereditary condition?
T Autti, M Muttilainen, R Raininko, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Neurology
|
May 22, 1998
Bright light suppresses melatonin in blind patients with neuronal ceroid-lipofuscinoses
T Hätönen, M L Laakso, H Heiskala, et al.
Acta Radiologica (Stockholm, Sweden : 1987)
|
March 10, 2009
Brain magnetic resonance imaging of siblings from families with two or more children with learning or intellectual disabilities and need for full-time special education
M Mannerkoski, H Heiskala, R Raininko, et al.
Brain & Development
|
November 1, 1996
West syndrome: individualized ACTH therapy
H Heiskala, R Riikonen, P Santavuori, et al.
American Journal of Medical Genetics
|
December 18, 2001
Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?
P Nokelainen, H Heiskala, R Raininko, et al.
Journal of Sleep Research
|
March 21, 2002
Neurological impairments and sleep-wake behaviour among the mentally retarded
N Lindblom, H Heiskala, M Kaski, et al.
Neuropediatrics
|
February 1, 1997
Brain perfusion SPECT abnormalities in neuronal ceroid lipofuscinoses
K Liewendahl, S L Vanhanen, H Heiskala, et al.
Neuropediatrics
|
February 1, 1997
Lamotrigine therapy in infantile neuronal ceroid lipofuscinosis (INCL)
L Aberg, H Heiskala, S L Vanhanen, et al.
Neuroreport
|
April 11, 2000
No evidence for extraocular light induced phase shifting of human melatonin, cortisol and thyrotropin rhythms
N Lindblom, H Heiskala, T Hätönen, et al.
American Journal of Medical Genetics
|
June 5, 1995
Circadian rhythm studies in neuronal ceroid-lipofuscinosis (NCL)
E Heikkilä, T H Hàtònen, T Telakivi, et al.
Annals of Neurology
|
June 9, 1999
Extensive cerebral white matter abnormality without clinical symptoms: a new hereditary condition?
T Autti, M Muttilainen, R Raininko, et al.
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of 3