Search Results - "Švojgr, K"

Therapy for Vitreous Seeding Caused by Retinoblastoma. A Review by Kodetová, M, Švojgr, K, Širc, J, Vaněček, J, Pochop, P

“…Retinoblastoma is the most common primary malignant intraocular tumor in children. Seeding, specifically the dispersion of the tumor into the adjacent…”
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Therapy for Vitreous Seeding Caused by Retinoblastoma. A Review by Kodetová, M, Švojgr, K, Širc, J, Vaněček, J, Pochop, P

“…Retinoblastoma is the most common primary malignant intraocular tumor in children. Seeding, specifically the dispersion of the tumor into the adjacent…”
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1411 Chemoreduction failure in D-E intraocular retinoblastoma, single center experience by Svojgr, K, Darsova, D, Kyncl, M, Malinova, B, Smelhaus, V, Stary, J, Pochop, P, Malis, J

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Is There a Higher Incidence of Sporadic Renal Angiomyolipoma in Childhood Cancer Survivors? by Kruseová, Jarmila, Gottfriedová, Barbora, Zichová, Andrea, Švojgr, Karel, Hošek, Petr, Lukš, Aleš, Kynčl, Martin, Eckschlager, Tomáš

“…Background: Cancer treatment can cause various long-term side effects, including those that impact ultrasound findings. During follow-up of childhood cancer…”
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Fanconi Anemia, Complementation Group D1 Caused by Biallelic Mutations of BRCA2 Gene--Case Report by Puchmajerová, A, Švojgr, K, Novotná, D, Macháčková, E, Sumerauer, D, Smíšek, P, Kodet, R, Kynčl, M, Křepelová, A, Foretová, L

“…Fanconi anemia is a rare autosomal recessive disorder, clinically and genetically heterogeneous, characterized by typical clinical features, such as short…”
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Hepatoblastoma, Etiology, Case Reports by Puchmajerová, A, Křepelová, A, Indráková, J, Sítková, R, Balaščak, I, Kruseová, J, Švojgr, K, Kodet, R, Kynčl, M, Vícha, A, Macek, Jr, M

“…Hepatoblastoma is an uncommon malignant neoplasm in general, yet, it is the most common liver malignancy in children with the incidence about one per milion…”
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Constitutively active Lyn kinase causes a cutaneous small vessel vasculitis and liver fibrosis syndrome by de Jesus, Adriana A., Chen, Guibin, Yang, Dan, Brdicka, Tomas, Ruth, Natasha M., Bennin, David, Cebecauerova, Dita, Malcova, Hana, Freeman, Helen, Martin, Neil, Svojgr, Karel, Passo, Murray H., Bhuyan, Farzana, Alehashemi, Sara, Rastegar, Andre T., Uss, Katsiaryna, Kardava, Lela, Marrero, Bernadette, Duric, Iris, Omoyinmi, Ebun, Peldova, Petra, Lee, Chyi-Chia Richard, Kleiner, David E., Hadigan, Colleen M., Hewitt, Stephen M., Pittaluga, Stefania, Carmona-Rivera, Carmelo, Calvo, Katherine R., Shah, Nirali, Balascakova, Miroslava, Fink, Danielle L., Kotalova, Radana, Parackova, Zuzana, Peterkova, Lucie, Kuzilkova, Daniela, Campr, Vit, Sramkova, Lucie, Biancotto, Angelique, Brooks, Stephen R., Manes, Cameron, Meffre, Eric, Harper, Rebecca L., Kuehn, Hyesun, Kaplan, Mariana J., Brogan, Paul, Rosenzweig, Sergio D., Merchant, Melinda, Deng, Zuoming, Huttenlocher, Anna, Moir, Susan L., Kuhns, Douglas B., Boehm, Manfred, Skvarova Kramarzova, Karolina, Goldbach-Mansky, Raphaela

“…Neutrophilic inflammation is a hallmark of many monogenic autoinflammatory diseases; pathomechanisms that regulate extravasation of damaging immune cells into…”
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The ECHO recommendations for dealing with vinblastine shortage affecting standard treatment of systemic Langerhans cell histiocytosis by Papadakis, Vassilios, Astigarraga, Itziar, den Bos, Cor, Donadieu, Jean, Henter, Jan‐Inge, Jacobs, Sandra, Lehrnbecher, Thomas, Munthe‐Kaas, Monica Cheng, Naeije, Leonie, Nanduri, Vasanta, Nguyen, Trung, Nysom, Karsten, Pears, Jane, Raciborska, Anna, Sieni, Elena, Svojgr, Karel, Tzotzola, Vasiliki, Minkov, Milen

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Nephroblastoma -  30-years period of its treatment in the University Hospital Motol, Prague by Mališ, J, Švojgr, K, Pýcha, K, Jeřábková, V, Cyprová, S, Churáčková, M, Šmelhaus, V, Radvanský, J, Zítková, M, Kodet, R, Kodetová, D, Malinová, B, Koutecký, J, Šnajdauf, J, Starý, J

“…Nephroblastoma (Wilms tumor - WT) is the most common solid tumor of kidney in children. We present treatment development of WT at the Department of Pediatric…”
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Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study by Kemps, Paul G., Zondag, Timo C. E., Arnardóttir, Helga B., Solleveld-Westerink, Nienke, Borst, Jelske, Steenwijk, Eline C., van Egmond, Demi, Swennenhuis, Joost F., Stelloo, Ellen, Trambusti, Irene, Verdijk, Robert M., van Noesel, Carel J. M., Cleven, Arjen H. G., Scheijde-Vermeulen, Marijn A., Koudijs, Marco J., Krsková, Lenka, Hawkins, Cynthia, Egeler, R. Maarten, Brok, Jesper, von Bahr Greenwood, Tatiana, Svojgr, Karel, Beishuizen, Auke, van Laar, Jan A. M., Pötschger, Ulrike, Hutter, Caroline, Sieni, Elena, Minkov, Milen, Abla, Oussama, van Wezel, Tom, van den Bos, Cor, van Halteren, Astrid G. S.

“…•Oncogenic mutation subtype appears an important driver of heterogeneity in clinical presentation of pediatric LCH.•Lesional BRAFV600E status is not a…”
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MAPK INHIBITORS IN CHILDREN WITH REFRACTORY HISTIOCYTOSIS: AN INTERNATIONAL STUDY OF 199 CASES by Donadieu, J, Evseev, D, Sieni, E, Slater, O, Hutter, C, van den Bos, C, Astigarraga, I, Lehrnbecher, T, Barkaoui, M, Holzhauer, S, Beutel, K, Garcia-Obregon, S, Kabbara, N, Milne, P, Helias, Z, Kolenova, A, Renard, C, Salmon, A, Hessissen, L, Golan, M, Elitzur, S, Ben Arush, M, Lustig, DA, Raciborska, A, Pagnier, A, Aladjidi, N, Malebranche, C, Plat, G, Ferster, A, Efremova, V, Blanc, L, Munthe-Kaas, MC, Henter, JI, Greenwood, TV, Felizzia, G, Braier, J, Lambilliote, A, Boudiaf, H, Svojgr, K, Zdenka, K, Bernard, F, Adam, C, Larabi, IA, Maschan, M, Bronin, G, Idbaih, A, Alvarez, JC, Novosad, O, Collin, M, Emile, JF, Minkov, M, Heritier, S

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Adaptor molecules expression in normal lymphopoiesis and in childhood leukemia by Svojgr, Karel, Burjanivova, Tatiana, Vaskova, Martina, Kalina, Tomas, Stary, Jan, Trka, Jan, Zuna, Jan

“…Abstract Transmembrane adaptor proteins are key mediators of antigen receptor signaling in lymphocytes. By influencing proliferation and differentiation, these…”
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Effets indésirables cutanés du vémurafénib dans la cohorte européenne d’enfants traités pour histiocytose langerhansienne réfractaire mutée B-RAF (V600E) by Tardieu, M., Néron, A., Duvert-Lehembre, S., Larbi, I.A., Visser, J., Hutter, C., Sieni, E., Kabbara, N., Barkaoui, M., Milne, P., Haroche, J., Hélias-Rodzewicz, Z., Jehanne, M., Kolenova, S., Pagnier, A., Templier, I., Charles, J., Leccia, M.-T., Plat, G., Lutun, A., Heisig, A., Ferster, A., Efremova, V., Blanc, L., Nicholson, J., Lambilliote, A., Lissat, A., Svojgr, K., Bernard, F., Aladjidi, N., Marie-Cardine, A., Idbaih, A., Slater, O., Minkov, M., Taly, V., Collin, M., Alvarez, J.-C., Emile, J.-F., Héritier, S., Donadieu, J.

“…L’histiocytose langerhansienne (HCL) est une pathologie essentiellement pédiatrique au pronostic très variable. La mutation somatique BRAF (V600E), identifiée…”
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