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G Karadima

Showing results (11-20 of 33) with videos related to

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Journal of the Neurological Sciences|May 28, 2019
Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek populationD Katsimpouris, C Kartanou, M Breza, et al.
American Journal of Medical Genetics|August 22, 2000
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndromeM B Petersen, G Karadima, M Samaritaki, et al.
American Journal of Medical Genetics|April 5, 2000
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotypeG Barbi, I Kennerknecht, G Wöhr, et al.
Neurology|February 21, 2007
APOE epsilon4 is associated with impaired verbal learning in patients with MSG Koutsis, M Panas, E Giogkaraki, et al.
Clinical Genetics|December 21, 2010
Huntington's disease in Greece: the experience of 14 yearsM Panas, G Karadima, E Vassos, et al.
Neuropsychobiology|April 5, 2001
Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onsetG Papadimitriou, D Dikeos, E Daskalopoulou, et al.
American Journal of Medical Genetics|May 30, 2001
GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: a genetic association studyG N Papadimitriou, D G Dikeos, G Karadima, et al.
Occupational and Environmental Medicine|November 15, 2000
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, IrelandG Dean, N C Nevin, M Mikkelsen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2026
Correction to: SCA27B: a treatable ataxia-from falls to independenceA Metridis, M Makrygianni, A Naka, et al.
American Journal of Medical Genetics|April 5, 2000
Molecular cytogenetic characterization and origin of two de novo duplication 9p casesA Tsezou, S Kitsiou, A Galla, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Journal of the Neurological Sciences|May 28, 2019
Screening for spinocerebellar ataxia type 36 (SCA36) in the Greek populationD Katsimpouris, C Kartanou, M Breza, et al.
American Journal of Medical Genetics|August 22, 2000
Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndromeM B Petersen, G Karadima, M Samaritaki, et al.
American Journal of Medical Genetics|April 5, 2000
Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotypeG Barbi, I Kennerknecht, G Wöhr, et al.
Neurology|February 21, 2007
APOE epsilon4 is associated with impaired verbal learning in patients with MSG Koutsis, M Panas, E Giogkaraki, et al.
Clinical Genetics|December 21, 2010
Huntington's disease in Greece: the experience of 14 yearsM Panas, G Karadima, E Vassos, et al.
Neuropsychobiology|April 5, 2001
Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onsetG Papadimitriou, D Dikeos, E Daskalopoulou, et al.
American Journal of Medical Genetics|May 30, 2001
GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: a genetic association studyG N Papadimitriou, D G Dikeos, G Karadima, et al.
Occupational and Environmental Medicine|November 15, 2000
Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, IrelandG Dean, N C Nevin, M Mikkelsen, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 9, 2026
Correction to: SCA27B: a treatable ataxia-from falls to independenceA Metridis, M Makrygianni, A Naka, et al.
American Journal of Medical Genetics|April 5, 2000
Molecular cytogenetic characterization and origin of two de novo duplication 9p casesA Tsezou, S Kitsiou, A Galla, et al.
Pageof 4