Evaluation of antithrombotic prophylaxis and thrombotic events in children with COVID-19 or MIS-C: A tertiary pediatric center experience von Guner Ozenen, G., Akaslan Kara, A., Boncuoglu, E., Kiymet, E., Cem, E., Sahinkaya, S., Yilmaz Celebi, M., Gulderen, M., Kacar, P., Uras, M., Hilkay Karapinar, T., Oymak, Y., Bayram, N., Devrim, I.

Volltext

Evaluating the Efficacy of Chemical Disinfectants on Contaminated Dental Materials Contaminated by An Airborne Disease Tuberculosis Similar to COVID-19 von Karaman, B, Balık, A, Cifter, E D, Balıkcı, A, Ozenen, G, Ozdemir-Ozenen, D, Ozdemir-Karatas, M

Volltext

Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphalocele von Arslan, S.Yildirim, Bal, Z.Sahbudak, Ozenen, G.Guner, Bilen, N.M., Naghiyev, J., Sakul, G., Ozkinay, F., Ergun, O., Ozarslan, A., Kurugol, Z.

Volltext

Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphalocele von Arslan, S Yildirim, Bal, Z Sahbudak, Ozenen, G Guner, Bilen, N M, Naghiyev, J, Sakul, G, Ozkinay, F, Ergun, O, Ozarslan, A, Kurugol, Z

Volltext

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta von Hart, PS, Becerik, S, Cogulu, D, Emingil, G, Ozdemir-Ozenen, D, Han, ST, Sulima, PP, Firatli, E, Hart, TC

Volltext

Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations von Jaureguiberry, G, De la Dure-Molla, M, Parry, D, Quentric, M, Himmerkus, N, Koike, T, Poulter, J, Klootwijk, E, Robinette, SL, Howie, AJ, Patel, V, Figueres, M-L, Stanescu, HC, Issler, N, Nicholson, JK, Bockenhauer, D, Laing, C, Walsh, SB, McCredie, DA, Povey, S, Asselin, A, Picard, A, Coulomb, A, Medlar, AJ, Bailleul-Forestier, I, Verloes, A, Le Caignec, C, Roussey, G, Guiol, J, Isidor, B, Logan, C, Shore, R, Johnson, C, Inglehearn, C, Al-Bahlani, S, Schmittbuhl, M, Clauss, F, Huckert, M, Laugel, V, Ginglinger, E, Pajarola, S, Spartà, G, Bartholdi, D, Rauch, A, Addor, M-C, Yamaguti, PM, Safatle, HP, Acevedo, AC, Martelli-Júnior, H, dos Santos Netos, PE, Coletta, RD, Gruessel, S, Sandmann, C, Ruehmann, D, Langman, CB, Scheinman, SJ, Ozdemir-Ozenen, D, Hart, TC, Hart, PS, Neugebauer, U, Schlatter, E, Houillier, P, Gahl, WA, Vikkula, M, Bloch-Zupan, A, Bleich, M, Kitagawa, H, Unwin, RJ, Mighell, A, Berdal, A, Kleta, R

Volltext bestellen

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations von Jaureguiberry, G, De la Dure-Molla, M, Parry, D, Quentric, M, Himmerkus, N, Koike, T, Poulter, J, Klootwijk, E, Robinette, SL, Howie, AJ, Patel, V, Figueres, ML, Stanescu, HC, Issler, N, Nicholson, JK, Bockenhauer, D, Laing, C, Walsh, SB, McCredie, DA, Povey, S, Asselin, A, Picard, A, Coulomb, A, Medlar, AJ, Bailleul-Forestier, I, Verloes, A, Le Caignec, C, Roussey, G, Guiol, J, Isidor, B, Logan, C, Shore, R, Johnson, C, Inglehearn, C, Al-Bahlani, S, Schmittbuhl, M, Clauss, F, Huckert, M, Laugel, V, Ginglinger, E, Pajarola, S, Spartà, G, Bartholdi, D, Rauch, A, Addor, MC, Yamaguti, PM, Safatle, HP, Acevedo, AC, Martelli-Júnior, H, dos Santos Netos, PE, Coletta, RD, Gruessel, S, Sandmann, C, Ruehmann, D, Langman, CB, Scheinman, SJ, Ozdemir-Ozenen, D, Hart, TC, Hart, PS, Neugebauer, U, Schlatter, E, Houillier, P, Gahl, WA, Vikkula, M, Bloch-Zupan, A, Bleich, M, Kitagawa, H, Unwin, RJ, Mighell, A, Berdal, A, Kleta, R

Volltext bestellen