CNS Malformations in the Newborn

por Barañano, Kristin, Burd, Irina
Publicado 2022

Using a smartphone on the move: do visual constraints explain why we slow walking speed?

por Rubio Barañano, Alejandro, Faisal, Muhammad, Barrett, Brendan T., Buckley, John G.
Publicado 2021

A neurodevelopmental disorder caused by a dysfunctional CACNA1A allele

por Kramer, Audra A., Bennett, Daniel F., Barañano, Kristin W., Bannister, Roger A.
Publicado 2023

Shock séptico y empiema por Pasteurella multocida

por Fernández Vecilla, Domingo, Unzaga, Miren Josebe, Barañano, Aspichueta, Cristina, de Tuesta, José Luis Díaz
Publicado 2021

Relapsing–remitting clinical course expands the phenotype of Aicardi–Goutières syndrome

por Lambe, Jeffrey, Murphy, Olwen C., Mu, Weiyi, Sondergaard Schatz, Krista, Barañano, Kristin W., Venkatesan, Arun
Publicado 2020

Serratia marcescens como causa de endoftalmitis tardía

por Vecilla, Domingo Fernández, Palacio, Paula Belén Blasco, Barañano, Miren Josebe Unzaga, de Tuesta, José Luis Díaz
Publicado 2020

Novel loss of function mutation in TUBA1A gene compromises tubulin stability and proteostasis causing spastic paraplegia and ataxia

por Zocchi, Riccardo, Bellacchio, Emanuele, Piccione, Michela, Scardigli, Raffaella, D’Oria, Valentina, Petrini, Stefania, Baranano, Kristin, Bertini, Enrico, Sferra, Antonella
Publicado 2023

Otomastoiditis tuberculosa: a propósito de un caso

por Ramos, Iris Sharon Pérez, Barañano, Miren Josebe Unzaga, Ruiz-Ogarrio, María Carmen Espallargas, Arco, José Luis Diaz De Tuesta Del
Publicado 2023

Neumonía asociada a derrame parapneumónico en paciente inmunocompetente causado por Bordetella bronchiseptica

por Vecilla, Domingo Fernández, Matheus, Mary Paz Roche, Hidalgo, Gotzon Iglesias, Barañano, Miren Josebe Unzaga, de Tuesta del Arco, José Luis Díaz
Publicado 2023

Two cases of Prevotella oris causing serious pleuropulmonary infections

por Vecilla, Domingo Fernández, Matheus, Mary Paz Roche, Hidalgo, Gotzon Iglesias, Zárraga, Estíbaliz Ugalde, Barañano, Miren Josebe Unzaga, del Arco, José Luis Díaz de Tuesta
Publicado 2023

MALDI Spectra Database for Rapid Discrimination and Subtyping of Mycobacterium kansasii

por Murugaiyan, Jayaseelan, Lewin, Astrid, Kamal, Elisabeth, Bakuła, Zofia, van Ingen, Jakko, Ulmann, Vit, Unzaga Barañano, Miren J., Humięcka, Joanna, Safianowska, Aleksandra, Roesler, Uwe H., Jagielski, Tomasz
Publicado 2018

VEGF Secreted by Hypoxic Müller Cells Induces MMP-2 Expression and Activity in Endothelial Cells to Promote Retinal Neovascularization in Proliferative Diabetic Retinopathy

por Rodrigues, Murilo, Xin, Xiaoban, Jee, Kathleen, Babapoor-Farrokhran, Savalan, Kashiwabuchi, Fabiana, Ma, Tao, Bhutto, Imran, Hassan, Syed Junaid, Daoud, Yassine, Baranano, David, Solomon, Sharon, Lutty, Gerard, Semenza, Gregg L., Montaner, Silvia, Sodhi, Akrit
Publicado 2013

Randomized Placebo-Controlled Trial Evaluating the Ophthalmic Safety of Single-Dose Tafenoquine in Healthy Volunteers

por Ackert, Jessica, Mohamed, Khadeeja, Slakter, Jason S., El-Harazi, Sherif, Berni, Alessandro, Gevorkyan, Hakop, Hardaker, Elizabeth, Hussaini, Azra, Jones, Siôn W., Koh, Gavin C. K. W., Patel, Jyoti, Rasmussen, Scott, Kelly, Deborah S., Barañano, David E., Thompson, John T., Warren, Keith A., Sergott, Robert C., Tonkyn, John, Wolstenholme, Allen, Coleman, Hanna, Yuan, Alex, Duparc, Stephan, Green, Justin A.
Publicado 2019

A genome-wide DNA methylation signature for SETD1B-related syndrome

por Krzyzewska, I. M., Maas, S. M., Henneman, P., Lip, K. v. d., Venema, A., Baranano, K., Chassevent, A., Aref-Eshghi, E., van Essen, A. J., Fukuda, T., Ikeda, H., Jacquemont, M., Kim, H.-G., Labalme, A., Lewis, S. M. E., Lesca, G., Madrigal, I., Mahida, S., Matsumoto, N., Rabionet, R., Rajcan-Separovic, E., Qiao, Y., Sadikovic, B., Saitsu, H., Sweetser, D. A., Alders, M., Mannens, M. M. A. M.
Publicado 2019

Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity

por Asselin, Laure, Rivera Alvarez, José, Heide, Solveig, Bonnet, Camille S., Tilly, Peggy, Vitet, Hélène, Weber, Chantal, Bacino, Carlos A., Baranaño, Kristin, Chassevent, Anna, Dameron, Amy, Faivre, Laurence, Hanchard, Neil A., Mahida, Sonal, McWalter, Kirsty, Mignot, Cyril, Nava, Caroline, Rastetter, Agnès, Streff, Haley, Thauvin-Robinet, Christel, Weiss, Marjan M., Zapata, Gladys, Zwijnenburg, Petra J. G., Saudou, Frédéric, Depienne, Christel, Golzio, Christelle, Héron, Delphine, Godin, Juliette D.
Publicado 2020

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

por Beck, David B., Basar, Mohammed A., Asmar, Anthony J., Thompson, Joyce J., Oda, Hirotsugu, Uehara, Daniela T., Saida, Ken, Pajusalu, Sander, Talvik, Inga, D’Souza, Precilla, Bodurtha, Joann, Mu, Weiyi, Barañano, Kristin W., Miyake, Noriko, Wang, Raymond, Kempers, Marlies, Tamada, Tomoko, Nishimura, Yutaka, Okada, Satoshi, Kosho, Tomoki, Dale, Ryan, Mitra, Apratim, Macnamara, Ellen, Matsumoto, Naomichi, Inazawa, Johji, Walkiewicz, Magdalena, Õunap, Katrin, Tifft, Cynthia J., Aksentijevich, Ivona, Kastner, Daniel L., Rocha, Pedro P., Werner, Achim
Publicado 2021

Pandemic intake questionnaire to improve quality, effectiveness, and efficiency of outpatient neurologic and developmental care at the Kennedy Krieger institute during the COVID-19...

por Vedmurthy, Pooja, Murray, Connor, Chen, Belinda, Asiedu, Akua, Baranano, Kristin, Bay, Mihee, Belcher, Harolyn, Burton, Vera, Conlon, Charles, Fine, Amena, Gill, Ryan, Harris, Jacqueline, Hart, Khaylynn, Inches, Shannon, Johnson, Jennifer, Lance, Eboni, Lipkin, Paul H., Menon, Deepa U., McIntyre, Tiffany, Rajaprakash, Meghna, Recio, Albert, Singer, Harvey S., Smegal, Lindsay, Smith-Hicks, Constance L., Vernon, Hilary, Wilms Floet, Anna Maria, Wong, Joyce, Yelin, Karina, Leppert, Mary L. O’Connor, Zabel, T. Andrew, Comi, Anne M.
Publicado 2022

TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development

por van Woerden, Geeske M., Bos, Melanie, de Konink, Charlotte, Distel, Ben, Avagliano Trezza, Rossella, Shur, Natasha E., Barañano, Kristin, Mahida, Sonal, Chassevent, Anna, Schreiber, Allison, Erwin, Angelika L., Gripp, Karen W., Rehman, Fatima, Brulleman, Saskia, McCormack, Róisín, de Geus, Gwynna, Kalsner, Louisa, Sorlin, Arthur, Bruel, Ange‐Line, Koolen, David A., Gabriel, Melissa K., Rossi, Mari, Fitzpatrick, David R., Wilkie, Andrew O.M., Calpena, Eduardo, Johnson, David, Brooks, Alice, van Slegtenhorst, Marjon, Fleischer, Julie, Groepper, Daniel, Lindstrom, Kristin, Innes, A. Micheil, Goodwin, Allison, Humberson, Jennifer, Noyes, Amanda, Langley, Katherine G., Telegrafi, Aida, Blevins, Amy, Hoffman, Jessica, Guillen Sacoto, Maria J., Juusola, Jane, Monaghan, Kristin G., Punj, Sumit, Simon, Marleen, Pfundt, Rolph, Elgersma, Ype, Kleefstra, Tjitske
Publicado 2021

Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms

por Yabumoto, Megan, Kianmahd, Jessica, Singh, Meghna, Palafox, Maria F., Wei, Angela, Elliott, Kathryn, Goodloe, Dana H., Dean, S. Joy, Gooch, Catherine, Murray, Brianna K., Swartz, Erin, Schrier Vergano, Samantha A., Towne, Meghan C., Nugent, Kimberly, Roeder, Elizabeth R., Kresge, Christina, Pletcher, Beth A., Grand, Katheryn, Graham, John M., Gates, Ryan, Gomez‐Ospina, Natalia, Ramanathan, Subhadra, Clark, Robin Dawn, Glaser, Kimberly, Benke, Paul J., Cohen, Julie S., Fatemi, Ali, Mu, Weiyi, Baranano, Kristin W., Madden, Jill A., Gubbels, Cynthia S., Yu, Timothy W., Agrawal, Pankaj B., Chambers, Mary‐Kathryn, Phornphutkul, Chanika, Pugh, John A., Tauber, Kate A., Azova, Svetlana, Smith, Jessica R., O’Donnell‐Luria, Anne, Medsker, Hannah, Srivastava, Siddharth, Krakow, Deborah, Schweitzer, Daniela N., Arboleda, Valerie A.
Publicado 2021