V. Čulić

发表

Platelet function analysis in children with Schönlein-Henoch syndrome.

D. Primorac, R. Jakl, S. Culić, 2001, Archives of medical research.

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

S. Janković, V. Pešutić-Pisac, S. Culić, 2003, Pediatric hematology and oncology.

Down syndrome: parental origin, recombination, and maternal age.

F. Béna, Z. Grubic, D. Pavlinić, 2012, Genetic testing and molecular biomarkers.

Single signal of the Williams syndrome chromosome region 1 gene in hyperploidic bone marrow cells of acute lymphoblastic leukemia in a Williams syndrome patient.

B. Peterlin, R. Lasan, S. Culić, 2002, Medical and pediatric oncology.

Complete trisomy 10p resulting from an extra stable telocentric chromosome

T. Zemunik, B. Lozić, R. Lasan, 2012, American journal of medical genetics. Part A.

Pneumococcal associated haemolytic uremic syndrome following invasive pneumococcal disease in a 2-year-old girl

S. Čulić, V. Čulić, D. Kuljiš, 2008 .

Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia.

N. Bošnjak, N. Barišić, J. Sertić, 1997, Collegium antropologicum.

Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice

B Peterlin, B. Peterlin, A. Maver, 2018, Clinical genetics.

The ophthalmic anomalies in children with Down syndrome in Split-Dalmatian County.

J. Pavelić, D. Karlica, Davor Galetović, 2011, Collegium antropologicum.

Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay

V. Fishman, I. Lebedev, E. Belyaeva, 2021, Cytogenetic and Genome Research.

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

T. Liehr, J. Pavelić, I. Lebedev, 2018, Cytogenetic and Genome Research.

Positive reproductive family history for spontaneous abortion: predictor for recurrent miscarriage in young couples.

J. Pavelić, P. Konjevoda, V. Čulić, 2012, European journal of obstetrics, gynecology, and reproductive biology.

Full trisomy 5 in a sample of spontaneous abortion and arias stella reaction

J. Pavelić, B. Lozić, V. Čulić, 2011, Medical science monitor : international medical journal of experimental and clinical research.

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

J. Pavelić, S. Culić, V. Čulić, 2010, Acta medica Okayama.

Identification of eight novel NSD1 mutations in Sotos syndrome

N. Niikawa, K. Yoshiura, N. Matsumoto, 2003, Journal of medical genetics.

DISSEMINATED BCG INFECTION RESEMBLING LANGERHANS CELL HISTIOCYTOSIS IN AN INFANT WITH SEVERE COMBINED IMMUNODEFICIENCY: A Case Report

S. Janković, R. Martinić, S. Culić, 2004, Pediatric hematology and oncology.

ETOPOSIDE AS THE BASIC AND INTERFERON-a AS THE MAINTENANCE THERAPY FOR LANGERHANS CELL HISTIOCYTOSIS: A RTC

D. Primorac, S. Čulić, M. Ščukanec-Špoljar, 2001, Pediatric hematology and oncology.

A Simple and Rapid Analysis of Triplet Repeat Diseases by Expand Long PCR

K. Pavelić, I. Barišić, V. Čulić, 2001, Clinical chemistry and laboratory medicine.

Fatal hepatic veno-occlusive disease with fibrinolysis as the cause of death during preoperative chemotherapy for nephroblastoma.

D. Primorac, J. de Kraker, S. Culić, 1998, Medical and pediatric oncology.

[Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge].

M. Baumgartner, S. Puseljic, I. Barić, 2011, Lijecnicki vjesnik.

The MECP2 Gene Mutation Screening in Rett Syndrome Patients from Croatia

J. Pavelić, J. Knežević, I. Barišić, 2006, Annals of the New York Academy of Sciences.

Treatment of post-traumatic trabecular mashwork thrombosis and secondary glaucoma with intracameral tissue plasminogen activator in previously unrecognized sickle cell anemia.

I. Salamunić, L. Znaor, I. Erceg, 2005, Collegium antropologicum.

Angiomyomatous Hamartoma of the Popliteal Lymph Nodes in a Patient with Klippel-Trenaunay Syndrome: Case Report

I. Jurić, J. Lamovec, I. K. Prusac, 2011, Fetal and pediatric pathology.

Three Cases of Joubert Syndrome in a Consanguineous Syrian Family and a Interesting Case of Multinational Collaboration

D. Petrović, V. Čulić, Zofia Swinderek-Alsayed, 2021, Journal of Pediatric Genetics.

Tyrosinemia type II (Richner-Hanhart syndrome): a new mutation in the TAT gene.

J. Pavelić, R. Betz, M. Refke, 2011, European journal of medical genetics.

Practical aspects of genetic counseling

P. Korošec, M. Cossée, N. Jokić-begić, 2007 .

A Croatian case of the Schinzel-Giedion syndrome.

R. Hennekam, J. Oorthuys, B. Rešić, 1996, Genetic Counseling.

Genitourinary diseases prior spontaneous abortion as a risk factor for recurrent pregnancy loss.

J. Pavelić, P. Konjevoda, G. Kardum, 2009, Collegium antropologicum.

Haplotype and AGG Interspersion Analysis of FMR1 Alleles in a Croatian Population: No Founder Effect Detected in Patients with Fragile X Syndrome

B. Lozić, I. Barišić, V. Čulić, 2008, Human biology.

PRENATAL DIAGNOSIS WITH GENETIC COUNSELING IN UHC SPLIT, CROATIA

J. Pavelić, D. Roje, I. Gunjača, 2017 .

Osteogenesis imperfecta - pamidronate treatment in Split Clinical Hospital Centre

J. Pavelić, Zdravka Rakuljić, V. Čulić, 2013 .