The first case of benign familial neonatal epilepsy diagnosed in Serbia

Autor: Marko Kojic, Katarina Nikolic, Milos M Jesic, D Maja Jesic

Publikováno v: Vojnosanitetski Pregled, Vol 78, Iss 9, Pp 1005-1008 (2021)

Introduction. The exact prevalence of Benign Familial Neonatal Epilepsy (BFNE) is unknown due to the likelyhood of overlooking the disease and not diagnosing affected patients correctly. The rare autosomal dominant inherited disorder occurs usually w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::822fe8500997de675ad1b891ab016e73
http://www.doiserbia.nb.rs/img/doi/0042-8450/2021/0042-84502000018N.pdf

Lipids on the Second Day in Ischemic and Normoxemic Term Neonates

Autor: Milos M Jesic, Svetlana J Milenkovic, Petar Ivanovski, Violeta V Bankovic, Tatjana V Nikolic, Biljana S Otaševic, Miljana Z. Jovandaric

Publikováno v: Fetal and Pediatric Pathology. 36:276-281

In hypoxic newborns requiring oxygen, lipid peroxidation affects the peripheral blood lipids.Determine the influence of perinatal oxygen therapy for hypoxia on serum lipid concentrations on the second day of life.Our study included 50 newborns with p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dbfe6ee3cd997e80d2a2f3570a0219c
https://doi.org/10.1080/15513815.2017.1313914

Neonatal Outcome in Pregnancies with Autoimmune Myasthenia Gravis

Autor: Maja Jesic, Miljana Z Jovandaric, Milos M Jesic, Dina J Despotovic

Publikováno v: Fetal and pediatric pathology. 35(3)

Introduction: Acquired autoimmune myasthenia gravis (MG) is an autoimmune process in which antibodies (AB) directed against the acetylcholine nicotinic receptor (AChR) cause weakness and fatigue of striated muscles. Objectives: The objective of this

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1e356494fe1582f0300e86dc771971d
https://pubmed.ncbi.nlm.nih.gov/27100475

Early onset of abdominal venous thrombosis in a newborn with homozygous type II heparin-binding site antithrombin deficiency.

Autor: Kovac M; aFaculty of Medicine, University of Belgrade bHemostasis Department, Blood Transfusion Institute of Serbia, Belgrade cMedical Faculty Novi Sad, University of Novi Sad Institute of Laboratory Medicine, Clinical Center of Vojvodina, Novi Sad dUniversity Children's Hospital, Belgrade eInstitute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Siberia fFaculty of Medicine, Division of Clinical Laboratory Research, Department of Laboratory Medicine, University of Debrecen, Debrecen, Hungary., Mitic G, Jesic M, Djordjevic V, Muszbek L, Bereczky Z

Publikováno v: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis [Blood Coagul Fibrinolysis] 2017 Apr; Vol. 28 (3), pp. 264-266.

Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity.

Autor: Daniel PB; Department of Women's and Children's Health, Dunedin School of Medicine, Otago University, Dunedin, New Zealand., Morgan T, Alanay Y, Bijlsma E, Cho TJ, Cole T, Collins F, David A, Devriendt K, Faivre L, Ikegawa S, Jacquemont S, Jesic M, Krakow D, Liebrecht D, Maitz S, Marlin S, Morin G, Nishikubo T, Nishimura G, Prescott T, Scarano G, Shafeghati Y, Skovby F, Tsutsumi S, Whiteford M, Zenker M, Robertson SP

Publikováno v: Human mutation [Hum Mutat] 2012 Apr; Vol. 33 (4), pp. 665-73. Date of Electronic Publication: 2012 Jan 23.