Time from ictal subdural EEG seizure onset to clinical seizure onset: Prognostic value for selecting temporal lobectomy candidates by Weinand, Martin E., Kester, Monica M., Labiner, David M., Ahern, Geoffrey L.

Get full text

Multisystem Inflammatory Syndrome in Children — Initial Therapy and Outcomes by Son, Mary Beth F, Murray, Nancy, Friedman, Kevin, Young, Cameron C, Newhams, Margaret M, Feldstein, Leora R, Loftis, Laura L, Tarquinio, Keiko M, Singh, Aalok R, Heidemann, Sabrina M, Soma, Vijaya L, Riggs, Becky J, Fitzgerald, Julie C, Kong, Michele, Doymaz, Sule, Giuliano, John S, Keenaghan, Michael A, Hume, Janet R, Hobbs, Charlotte V, Schuster, Jennifer E, Clouser, Katharine N, Hall, Mark W, Smith, Lincoln S, Horwitz, Steven M, Schwartz, Stephanie P, Irby, Katherine, Bradford, Tamara T, Maddux, Aline B, Babbitt, Christopher J, Rowan, Courtney M, McLaughlin, Gwenn E, Yager, Phoebe H, Maamari, Mia, Mack, Elizabeth H, Carroll, Christopher L, Montgomery, Vicki L, Halasa, Natasha B, Cvijanovich, Natalie Z, Coates, Bria M, Rose, Charles E, Newburger, Jane W, Patel, Manish M, Randolph, Adrienne G

Request full text

The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children by Benamar, Mehdi, Chen, Qian, Chou, Janet, Julé, Amélie M, Boudra, Rafik, Contini, Paola, Crestani, Elena, Lai, Peggy S, Wang, Muyun, Fong, Jason, Rockwitz, Shira, Lee, Pui, Chan, Tsz Man Fion, Altun, Ekin Zeynep, Kepenekli, Eda, Karakoc-Aydiner, Elif, Ozen, Ahmet, Boran, Perran, Aygun, Fatih, Onal, Pinar, Sakalli, Ayse Ayzit Kilinc, Cokugras, Haluk, Gelmez, Metin Yusuf, Oktelik, Fatma Betul, Cetin, Esin Aktas, Zhong, Yuelin, Taylor, Maria Lucia, Irby, Katherine, Halasa, Natasha B, Mack, Elizabeth H, Signa, Sara, Prigione, Ignazia, Gattorno, Marco, Cotugno, Nicola, Amodio, Donato, Geha, Raif S, Son, Mary Beth, Newburger, Jane, Agrawal, Pankaj B, Volpi, Stefano, Palma, Paolo, Kiykim, Ayca, Randolph, Adrienne G, Deniz, Gunnur, Baris, Safa, De Palma, Raffaele, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Henderson, Lauren A, Chatila, Talal A

Get full text

Germline Mutations of the MEN1 Gene in Familial Multiple Endocrine Neoplasia Type 1 and Related States by Agarwal, Sunita K., Beth Kester, Mary, Debelenko, Larisa V., Heppner, Christina, Emmert-Buck, Michael R., Skarulis, Monica C., Doppman, John L., Kim, Young S., Lubensky, Irina A., Zhuang, Zhengping, Green, Jane S., Guru, Sirandanahalli C., Manickam, Pachiappan, Olufemi, Shodimu-Emmanuel, Liotta, Lance A., Chandrasekharappa, Settara C., Collins, Francis S., Spiegel, Allen M., Lee Burns, A., Marx, Stephen J.

Get full text

Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas by ZHUANG, Z, VORTMEYER, A. O, GURU, S. C, MANICKAM, P, OLUFEMI, S.-E, YU, F, HEPPNER, C, CRABTREE, J. S, SKARULIS, M. C, VENZON, D. J, EMMERT-BUCK, M. R, SPIEGEL, A. M, PACK, S, CHANDRASEKHARAPPA, S. C, COLLINS, F. S, BURNS, A. L, MARX, S. J, JENSEN, R. T, LIOTTA, L. A, LUBENSKY, I. A, HUANG, S, PHAM, T. A, WANG, C, PARK, W.-S, AGARWAL, S. K, DEBELENKO, L. V, KESTER, M

Get full text

Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families by Agarwal, Sunita K., Debelenko, Larisa V., Kester, Mary Beth, Guru, Siradanahalli C., Manickam, Pachiappan, Olufemi, Shodimu-Emmanuel, Skarulis, Monica C., Heppner, Christina, Crabtree, Judy S., Lubensky, Irina A., Zhuang, Zhengping, Kim, Young S., Chandrasekharappa, Settara C., Collins, Francis S., Liotta, Lance A., Spiegel, Allen M., Burns, A. Lee, Emmert-Buck, Michael R., Marx, Stephen J.

Get full text

11q13 Allelotype Analysis in 27 Northern American MEN1 Kindreds Identifies Two Distinct Founder Chromosomes by Emmert-Buck, Michael R., Debelenko, Larisa V., Agarwal, Sunita, Kester, Mary Beth, Manickam, Pachiappan, Zhuang, Zhengping, Guru, Siradanahalli C., Olufemi, Shodimu-Emmanuel, Burns, A.Lee, Chandrasekharappa, Settara C., Lubensky, Irina A., Liotta, Lance A., Skarulis, Monica C., Spiegel, Allen M., Marx, Stephen J., Collins, Francis S.

Get full text

Analysis of recurrent germline mutations in theMEN1 gene encountered in apparently unrelated families by Agarwal, Sunita K., Debelenko, Larisa V., Kester, Mary Beth, Guru, Siradanahalli C., Manickam, Pachiappan, Olufemi, Shodimu-Emmanuel, Skarulis, Monica C., Heppner, Christina, Crabtree, Judy S., Lubensky, Irina A., Zhuang, Zhengping, Kim, Young S., Chandrasekharappa, Settara C., Collins, Francis S., Liotta, Lance A., Spiegel, Allen M., Burns, A. Lee, Emmert-Buck, Michael R., Marx, Stephen J.

Get full text