Publications by authors named "Vida Culic"

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Three Cases of Joubert Syndrome in a Consanguineous Syrian Family and a Interesting Case of Multinational Collaboration.
Davor Petrović, Vida Čulić, Zofia Swinderek-Alsayed

J Pediatr Genet· June 2023

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Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay.
Stanislav A Vasilyev, Nikolay A Skryabin, Anna A Kashevarova, Ekaterina N Tolmacheva, Renata R Savchenko

Cytogenet Genome Res· August 2021

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A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss.
Vida Čulić, Ruzica Lasan-Trcić, Thomas Liehr, Igor N Lebedev, Maja Pivić

Cytogenet Genome Res· February 2019

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Distal arthrogryposis with variable clinical expression caused by mutation.
Vida Čulić, Noriko Miyake, Sunčana Janković, Davor Petrović, Marko Šimunović

Hum Genome Var· October 2016

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Complete trisomy 10p resulting from an extra stable telocentric chromosome.
Bernarda Lozić, Vida Culić, Ružica Lasan, Maja Tomasović, Radenka Kuzmanić Samija

Am J Med Genet A· July 2012

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Positive reproductive family history for spontaneous abortion: predictor for recurrent miscarriage in young couples.
Silvana Miskovic, Vida Culic, Pasko Konjevoda, Jasminka Pavelic

Eur J Obstet Gynecol Reprod Biol· April 2012

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Down syndrome: parental origin, recombination, and maternal age.
Jadranka Vraneković, Ivana Babić Božović, Zorana Grubić, Jasenka Wagner, Dinko Pavlinić

Genet Test Mol Biomarkers· January 2012

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Angiomyomatous hamartoma of the popliteal lymph nodes in a patient with Klippel-Trenaunay syndrome: case report.
Ivana Kuzmic Prusac, Ivo Juric, Janez Lamovec, Vida Culic

Fetal Pediatr Pathol· December 2011

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The ophthalmic anomalies in children with Down syndrome in Split-Dalmatian County.
Dobrila Karlica, Sinisa Skelin, Vida Culic, Davor Galetović, Ljubo Znaor

Coll Antropol· December 2011

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Full trisomy 5 in a sample of spontaneous abortion and Arias Stella reaction.
Vida Čulić, Bernarda Lozic, Ivana Kuzmić-Prusac, Goran Mijaljica, Jasminka Pavelić

Med Sci Monit· October 2011

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Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene.
Vida Culic, Regina C Betz, Melanie Refke, Ksenija Fumic, Jasminka Pavelic

Eur J Med Genet· September 2011

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[Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge].
Karin Juras, Ksenija Fumić, Senka Izaković, Silvija Puseljić, Vida Culić

Lijec Vjesn· June 2011

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Common acute lymphoblastic leukemia Ph+ following Langerhans cell histiocytosis in a multi-malformed child with INV (9) (p12;q13) (mat): case report.
Jasminka Pavelić, Srdjana Culić, Vida Culić

Acta Med Okayama· August 2010

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Genitourinary diseases prior spontaneous abortion as a risk factor for recurrent pregnancy loss.
Vida Culić, Pasko Konjevoda, Kornelija Mise, Goran Kardum, Tanja Matijević

Coll Antropol· March 2009

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De novo NEMO gene deletion (delta4-10)--a cause of incontinentia pigmenti in a female infant: a case report.
Vida Culić, Dragana Gabrić, Neira Puizina-Ivić, Katja Rozman, Borut Peterlin

Coll Antropol· December 2008

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The MECP2 gene mutation screening in Rett syndrome patients from Croatia.
Tanja Matijević, Jelena Knezević, Ingeborg Barisić, Biserka Resić, Vida Culić

Ann N Y Acad Sci· December 2006

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Treatment of post-traumatic trabecular mashwork thrombosis and secondary glaucoma with intracameral tissue plasminogen activator in previously unrecognized sickle cell anemia.
Ksenija Karaman, Srdjana Culić, Ivana Erceg, Vida Culić, Alen Siniilć

Coll Antropol· October 2005

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Disseminated BCG infection resembling langerhans cell histiocytosis in an infant with severe combined immunodeficiency: a case report.
Srdjana Culic, Ivana Kuzmic, Vida Culic, Roko Martinic, Dubravka Kuljis

Pediatr Hematol Oncol· September 2004

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Anti-CD20 monoclonal antibody (Rituximab) for therapy of mediastinal CD20-positive large B-cell non-Hodgkin lymphoma with a local tumor extension into the lung of a 10-year-old girl.
Srdjana Culić, Vida Culić, Visnja Armanda, Dubravka Kuljis, Valdi Pesutić-Pisac

Pediatr Hematol Oncol· June 2003

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"Two hits" in utero?
Vida Culic, Srdjana Culic, Biserka Reisic

Med Pediatr Oncol· April 2003

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Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient.
Vida Culic, Srdjana Culic, Visnja Armanda, Biserka Resic, Ruzica Lasan

Med Pediatr Oncol· March 2002

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