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V Anastasiadou

Showing results (1-10 of 15) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Ineffectiveness of captopril in reducing cystine excretion in cystinuric childrenH Michelakakis, D Delis, V Anastasiadou, et al.
Clinical Genetics|January 26, 2007
Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in CyprusM Loizidou, Y Marcou, V Anastasiadou, et al.
Human Genetics|August 1, 1994
Mutation analysis of a Sandhoff disease patient in the Maronite community in CyprusY Hara, P Ioannou, A Drousiotou, et al.
Human Mutation|January 15, 1999
Novel splice site mutation at IVS8 nt 5 of HEXB responsible for a Greek-Cypriot case of Sandhoff diseaseK Furihata, A Drousiotou, Y Hara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 29, 2015
Genetic findings of Cypriot spinal muscular atrophy patientsL Theodorou, P Nicolaou, P Koutsou, et al.
Hormones (Athens, Greece)|October 15, 2013
Sex steroids and sex hormone-binding globulin in postmenopausal women with nonalcoholic fatty liver diseaseStergios A Polyzos, Jannis Kountouras, Agathocles Tsatsoulis, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiologyP C Patsalis, C Sismani, M I Hadjimarcou, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Genetic predisposition and IDDM in GreeceC Karayanni, V Anastasiadou, M Spyropoulou, et al.
Journal of Endocrinological Investigation|March 23, 2011
RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2V Neocleous, N Skordis, G Portides, et al.
Human Mutation|March 29, 2000
Geographical clustering of low density lipoprotein receptor gene mutations (C292X; Q363X; D365E & C660X) in CyprusS L Xenophontos, A Pierides, K Demetriou, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|January 1, 1993
Ineffectiveness of captopril in reducing cystine excretion in cystinuric childrenH Michelakakis, D Delis, V Anastasiadou, et al.
Clinical Genetics|January 26, 2007
Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in CyprusM Loizidou, Y Marcou, V Anastasiadou, et al.
Human Genetics|August 1, 1994
Mutation analysis of a Sandhoff disease patient in the Maronite community in CyprusY Hara, P Ioannou, A Drousiotou, et al.
Human Mutation|January 15, 1999
Novel splice site mutation at IVS8 nt 5 of HEXB responsible for a Greek-Cypriot case of Sandhoff diseaseK Furihata, A Drousiotou, Y Hara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 29, 2015
Genetic findings of Cypriot spinal muscular atrophy patientsL Theodorou, P Nicolaou, P Koutsou, et al.
Hormones (Athens, Greece)|October 15, 2013
Sex steroids and sex hormone-binding globulin in postmenopausal women with nonalcoholic fatty liver diseaseStergios A Polyzos, Jannis Kountouras, Agathocles Tsatsoulis, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiologyP C Patsalis, C Sismani, M I Hadjimarcou, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Genetic predisposition and IDDM in GreeceC Karayanni, V Anastasiadou, M Spyropoulou, et al.
Journal of Endocrinological Investigation|March 23, 2011
RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2V Neocleous, N Skordis, G Portides, et al.
Human Mutation|March 29, 2000
Geographical clustering of low density lipoprotein receptor gene mutations (C292X; Q363X; D365E & C660X) in CyprusS L Xenophontos, A Pierides, K Demetriou, et al.
Pageof 2