Search Results - "PASIC, Srdjan"

Safety and efficacy of an oral histone deacetylase inhibitor in systemic‐onset juvenile idiopathic arthritis by Vojinovic, Jelena, Damjanov, Nemanja, D'Urzo, Carmine, Furlan, Antonio, Susic, Gordana, Pasic, Srdjan, Iagaru, Nicola, Stefan, Mariana, Dinarello, Charles A.

“…Objective The current treatment options for systemic‐onset juvenile idiopathic arthritis (JIA) are methotrexate, steroids, and biologic agents. This study was…”
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Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome by Minegishi, Yoshiyuki, Saito, Masako, Tsuchiya, Shigeru, Tsuge, Ikuya, Takada, Hidetoshi, Hara, Toshiro, Kawamura, Nobuaki, Ariga, Tadashi, Pasic, Srdjan, Stojkovic, Oliver, Metin, Ayse, Karasuyama, Hajime

“…Hyper-immunoglobulin E syndrome (HIES) is a compound primary immunodeficiency characterized by a highly elevated serum IgE, recurrent staphylococcal skin…”
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Mechanisms of redox balance and inflammatory response after the use of methylprednisolone in children with multisystem inflammatory syndrome associated with COVID-19 by Krasic, Stasa, Vukomanovic, Vladislav, Ninic, Sanja, Pasic, Srdjan, Samardzija, Gordana, Mitrovic, Nemanja, Cehic, Maja, Nesic, Dejan, Bajcetic, Milica

“…BackgroundMultisystem inflammatory syndrome in children (MIS-C) associated with being infected with coronavirus-19 (COVID-19) is a life-threatening condition…”
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Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity by Minegishi, Yoshiyuki, Saito, Masako, Morio, Tomohiro, Watanabe, Ken, Agematsu, Kazunaga, Tsuchiya, Shigeru, Takada, Hidetoshi, Hara, Toshiro, Kawamura, Nobuaki, Ariga, Tadashi, Kaneko, Hideo, Kondo, Naomi, Tsuge, Ikuya, Yachie, Akihiro, Sakiyama, Yukio, Iwata, Tsutomu, Bessho, Fumio, Ohishi, Tsutomu, Joh, Kosuke, Imai, Kohsuke, Kogawa, Kazuhiro, Shinohara, Miwa, Fujieda, Mikiya, Wakiguchi, Hiroshi, Pasic, Srdjan, Abinun, Mario, Ochs, Hans D., Renner, Eleonore D., Jansson, Annette, Belohradsky, Bernd H., Metin, Ayse, Shimizu, Norio, Mizutani, Shuki, Miyawaki, Toshio, Nonoyama, Shigeaki, Karasuyama, Hajime

“…Tyrosine kinase 2 (Tyk2) is a nonreceptor tyrosine kinase that belongs to the Janus kinase (Jak) family. Here we identified a homozygous Tyk2 mutation in a…”
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Case Report: Early Onset Systemic Lupus Erythematosus Due to Hereditary C1q Deficiency Treated With Fresh Frozen Plasma by Zecevic, Milica, Minic, Aleksandra, Pasic, Srdjan, Perovic, Vladimir, Prohászka, Zoltán

“…Hereditary C1q deficiency is associated with early-onset autoimmunity causing SLE or SLE-like disease as well as increased risk for infections with…”
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Analysis of cardiac manifestation and treatment of multisystem inflammatory syndrome in children related to SARS-CoV-2 by Krasic, Stasa, Ninic, Sanja, Prijic, Sergej, Popovic, Sasa, Pasic, Srdjan, Petrovic, Gordana, Zec, Boris, Ristic, Snezana, Nesic, Dejan, Nikolic, Luka, Vukomanovic, Vladislav

“…Cardiovascular manifestations are common (35-100%) in the multisystem inflammatory syndrome in children. Our study aimed to analyze treatment impact and…”
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Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency by Walter, Jolan E, Rucci, Francesca, Patrizi, Laura, Recher, Mike, Regenass, Stephan, Paganini, Tiziana, Keszei, Marton, Pessach, Itai, Lang, Philipp A, Poliani, Pietro Luigi, Giliani, Silvia, Al-Herz, Waleed, Cowan, Morton J, Puck, Jennifer M, Bleesing, Jack, Niehues, Tim, Schuetz, Catharina, Malech, Harry, DeRavin, Suk See, Facchetti, Fabio, Gennery, Andrew R, Andersson, Emma, Kamani, Naynesh R, Sekiguchi, JoAnn, Alenezi, Hamid M, Chinen, Javier, Dbaibo, Ghassan, ElGhazali, Gehad, Fontana, Adriano, Pasic, Srdjan, Detre, Cynthia, Terhorst, Cox, Alt, Frederick W, Notarangelo, Luigi D

“…The contribution of B cells to the pathology of Omenn syndrome and leaky severe combined immunodeficiency (SCID) has not been previously investigated. We have…”
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Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles by Kamae, Chikako, MD, Nakagawa, Noriko, MD, PhD, Sato, Hiroki, MS, Honma, Kenichi, MD, Mitsuiki, Noriko, MD, Ohara, Osamu, PhD, Kanegane, Hirokazu, MD, PhD, Pasic, Srdjan, MD, PhD, Pan-Hammarström, Qiang, MD, PhD, van Zelm, Menno C., PhD, Morio, Tomohiro, MD, PhD, Imai, Kohsuke, MD, PhD, Nonoyama, Shigeaki, MD, PhD

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Recombinase-activating gene 1 immunodeficiency: different immunological phenotypes in three siblings by Pasic, Srdjan, Djuricic, Slavisa, Ristic, Goran, Slavkovic, Bojana

“…We report different immunological phenotypes in three siblings from consanguineous family with recombinase‐activating gene 1 (RAG1) gene mutations. Null…”
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Treatment of the X-linked lymphoproliferative, Griscelli and Chédiak-Higashi syndromes by HLH directed therapy by Trottestam, Helena, Beutel, Karin, Meeths, Marie, Carlsen, Niels, Heilmann, Carsten, Pašić, Srdjan, Webb, David, Hasle, Henrik, Henter, Jan-Inge

“…Background Griscelli syndrome type 2 (GS2), the X‐linked lymphoproliferative (XLP) and the Chédiak–Higashi (CHS) syndromes are diseases that all may develop…”
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Therapeutic approaches for the treatment of renal disease in juvenile systemic lupus erythematosus: an international multicentre PRINTO study by Miettunen, Paivi M, Pistorio, Angela, Palmisani, Elena, Ravelli, Angelo, Silverman, Earl, Oliveira, Sheila, Alessio, Maria, Cuttica, Ruben, Mihaylova, Dimitrina, Espada, Graciela, Pasic, Srdjan, Insalaco, Antonella, Ozen, Seza, Porras, Oscar, Sztajnbok, Flavio, Lazarevic, Dragana, Martini, Alberto, Ruperto, Nicolino

“…To evaluate therapeutic approaches and response to therapy in juvenile systemic lupus erythematosus (SLE) with renal involvement in a large prospective…”
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Severe Combined Immunodeficiency in Serbia and Montenegro Between Years 1986 and 2010: A Single-Center Experience by Pasic, Srdjan, Vujic, Dragana, Veljković, Dobrila, Slavkovic, Bojana, Mostarica-Stojkovic, Marija, Minic, Predrag, Minic, Aleksandra, Ristic, Goran, Giliani, Silvia, Villa, Anna, Sobacchi, Cristina, Lilić, Desa, Abinun, Mario

“…Severe combined immunodeficiency (SCID), including the ‘variant’ Omenn syndrome (OS), represent a heterogeneous group of monogenic disorders characterized by…”
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Central Nervous System Involvement in Hemophagocytic Lymphohistiocytosis: A Single-Center Experience by Jovanovic, Ankica, MD, Kuzmanovic, Milos, MD, Kravljanac, Ruzica, MD, Micic, Dragan, MD, Jovic, Milena, MD, Gazikalovic, Slobodan, MD, Pasic, Srdjan, MD

“…Abstract Background Hemophagocytic lymphohistiocytosis is a rare multisystem disorder characterized by proliferation and diffuse infiltration multiple organs…”
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Pancreatitis and atypical Kawasaki disease by Prokic, Dragan, Ristic, Goran, Paunovic, Zoran, Pasic, Srdjan

“…We report on pediatric patient with clinical and laboratory evidence of pancreatitis at onset of atypical Kawasaki disease (KD). In KD pancreatic inflammation…”
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Disseminated neonatal herpes caused by herpes simplex virus types 1 and 2 by Knezevic, Aleksandra, Martic, Jelena, Stanojevic, Maja, Jankovic, Sasa, Nedeljkovic, Jasminka, Nikolic, Ljubica, Pasic, Srdjan, Jankovic, Borisav, Jovanovic, Tanja

“…Disseminated neonatal herpes simplex virus (HSV) infection is characterized by progressive multiple organ failure and high mortality rates. It can result from…”
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The use of tocilizumab in a child with systemic onset juvenile idiopathic arthritis and ganglioneuroblastoma by Goran, Ristic, Dragutin, Djokic, Srdjan, Pasic

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Atypical Strain of Toxoplasma gondii Causing Fatal Reactivation after Hematopoietic Stem Cell Transplantion in a Patient with an Underlying Immunological Deficiency by Stajner, Tijana, Vasiljevic, Zorica, Vujic, Dragana, Markovic, Marija, Ristic, Goran, Micic, Dragan, Pasic, Srdjan, Ivovic, Vladimir, Ajzenberg, Daniel, Djurkovic-Djakovic, Olgica

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N-Terminal RAG1 Frameshift Mutations in Omenn's Syndrome: Internal Methionine Usage Leads to Partial V(D)J Recombination Activity and Reveals a Fundamental Role In vivo for the N-Terminal Domains by Santagata, S, Gomez, C A, Sobacchi, C, Bozzi, F, Abinun, M, Pasic, S, Cortes, P, Vezzoni, P, Villa, A

“…Omenn's syndrome is an autosomal recessive primary immunodeficiency characterized by variable numbers of T lymphocytes of limited clonality, hypereosinophilia,…”
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Association of Antiphospholipid Antibodies with Clinical Manifestations in Children with Systemic Lupus Erythematosus by Petrovic, Gordana, Pasic, Srdjan, Soldatovic, Ivan

“…The aim of the study is to evaluate the effect of the presence of antiphospholipid antibodies on the clinical and laboratory manifestations, disease activity…”
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Fulminant subacute sclerosing panencephalitis:two cases with atypical presentation by Marjanović, Borivoj D, Stojanov, Ljubomir M, Zamurović, Dragan R, Pasić, Srdjan S, Kravljanac, Ružica M, Djordjevi, Maja S

“…From 1972 to 2002, we diagnosed and treated 22 cases of subacute sclerosing panencephalitis. We report on two pediatric patients with fulminant subacute…”
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