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Movement Disorders : Official Journal of the Movement Disorder Society
|
March 29, 2002
Myoclonic status epilepticus: video presentation
Aman Badhwar, Auli Siren, Eva Andermann, et al.
Molecular Genetics & Genomic Medicine
|
July 5, 2018
Signs indicating dementia in Down, Williams and Fragile X syndromes
Oili Sauna-Aho, Nina Bjelogrlic-Laakso, Auli Siren, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
November 26, 2002
Idiopathic generalised epilepsies with 3 Hz and faster spike wave discharges: a population-based study with evaluation and long-term follow-up in 71 patients
Auli Siren, Kai Eriksson, Heli Jalava, et al.
Epilepsy Research
|
September 12, 2013
A new locus for familial temporal lobe epilepsy on chromosome 3q
Lyne Chahine, Bassel Abou-Khalil, Auli Siren, et al.
Molecular Genetics & Genomic Medicine
|
May 13, 2021
Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders
Hannaleena Kokkonen, Auli Siren, Tuomo Määttä, et al.
Scientific Reports
|
May 16, 2024
Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders
Isabelle Schrauwen, Yasmin Rajendran, Anushree Acharya, et al.
Cephalalgia : an International Journal of Headache
|
February 15, 2022
<i>NCOR2</i> is a novel candidate gene for migraine-epilepsy phenotype
Marjo Eveliina Nuottamo, Paavo Häppölä, Ville Artto, et al.
Epilepsy Research
|
March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q
Robert Robinson, Nichole Taske, Thomas Sander, et al.
Human Genetics
|
March 12, 2021
Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland
Irma Järvelä, Tuomo Määttä, Anushree Acharya, et al.
Epilepsia
|
January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
, Costin Leu, Carolien G F de Kovel, et al.
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of 2
Search research articles
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Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 29, 2002
Myoclonic status epilepticus: video presentation
Aman Badhwar, Auli Siren, Eva Andermann, et al.
Molecular Genetics & Genomic Medicine
|
July 5, 2018
Signs indicating dementia in Down, Williams and Fragile X syndromes
Oili Sauna-Aho, Nina Bjelogrlic-Laakso, Auli Siren, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
November 26, 2002
Idiopathic generalised epilepsies with 3 Hz and faster spike wave discharges: a population-based study with evaluation and long-term follow-up in 71 patients
Auli Siren, Kai Eriksson, Heli Jalava, et al.
Epilepsy Research
|
September 12, 2013
A new locus for familial temporal lobe epilepsy on chromosome 3q
Lyne Chahine, Bassel Abou-Khalil, Auli Siren, et al.
Molecular Genetics & Genomic Medicine
|
May 13, 2021
Identification of microduplications at Xp21.2 and Xq13.1 in neurodevelopmental disorders
Hannaleena Kokkonen, Auli Siren, Tuomo Määttä, et al.
Scientific Reports
|
May 16, 2024
Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders
Isabelle Schrauwen, Yasmin Rajendran, Anushree Acharya, et al.
Cephalalgia : an International Journal of Headache
|
February 15, 2022
<i>NCOR2</i> is a novel candidate gene for migraine-epilepsy phenotype
Marjo Eveliina Nuottamo, Paavo Häppölä, Ville Artto, et al.
Epilepsy Research
|
March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q
Robert Robinson, Nichole Taske, Thomas Sander, et al.
Human Genetics
|
March 12, 2021
Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland
Irma Järvelä, Tuomo Määttä, Anushree Acharya, et al.
Epilepsia
|
January 17, 2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
, Costin Leu, Carolien G F de Kovel, et al.
Page
of 2