Mucosal Scalping of a Subepithelial Lesion: A Naked Colonic Lymphangioma

por Zimmer, Vincent, Eltze, Elke
Publicado 2019

A Curious Case of Coil-Angitis

por Beard, Jasna I., Murphy, Sharif, Philips, George
Publicado 2019

Rare Co-occurrence of Eosinophilic Esophagitis and Type 2B von Willebrand Disease: Implications for Endoscopic Surveillance and Esophageal Dilation

por Corder, S. Ryanne, Weston, Brent W., Dellon, Evan S.
Publicado 2019

Cloacogenic Polyps

por Marcos, Pedro, Eliseu, Liliana, Cunha, Maria Fernanda, Vasconcelos, Helena
Publicado 2019

Combined Immunodeficiency With Inflammatory Bowel Disease in a Patient With TTC7A Deficiency

por Broome, David T., Young, Andrew, Torbic, Heather, Krishnan, Sudhir, Gordon, Ilyssa, Lai, Keith, Rizk, Maged, Rieder, Florian
Publicado 2019

Hepatoid Adenocarcinoma of the Rectum With Liver Metastasis in a Patient With Ulcerative Colitis

por Levy, Alexander N., Ackerman, Rachel, Yilmaz, Osman, Jouhourian, Caroline, Tandon, Manish, Winter, Michael W.
Publicado 2019

Cryptogenic Multifocal Ulcerative Sclerosing Enteritis: A Curious Case of Intestinal Obstruction in the Setting of Human Immunodeficiency Virus

por Hathorn, Kelly, Qazi, Taha, Caton, Michael Travis, Allegretti, Jessica R.
Publicado 2019

Intussusception After Pancreaticoduodenectomy

por Patel, Kishan, Luthra, Anjuli, Aberra, Fasika, Lara, Luis F., Gray, Darrell
Publicado 2019

Protein-Losing Enteropathy as the Initial Presentation of Gastrointestinal Kaposi's Sarcoma in Previously Undiagnosed HIV Disease

por Curras-Martin, Diana, Campbell, Natasha, Copca-Alvarez, Albino, Casey, Kathleen, Lerner, William A., Hossain, Mohammad A.
Publicado 2019

Sigmoid Volvulus as the Initial Presentation of Chronic Intestinal Schistosomiasis

por Ilyas, Ghulam, Alawad, Mouyed, Baqir, Agha Wajdan, Oza, Twisha
Publicado 2019

Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencing

por Krenn, Martin, Milenkovic, Ivan, Eckstein, Gertrud, Zimprich, Fritz, Meitinger, Thomas, Foki, Thomas, Wagner, Matias
Publicado 2019

Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series

por Andréasson, Mattias, Lagerstedt-Robinson, Kristina, Samuelsson, Kristin, Solders, Göran, Blennow, Kaj, Paucar, Martin, Svenningsson, Per
Publicado 2019

New family with HSPB8-associated autosomal dominant rimmed vacuolar myopathy

por Al-Tahan, Sejad, Weiss, Lan, Yu, Howard, Tang, Sha, Saporta, Mario, Vihola, Anna, Mozaffar, Tahseen, Udd, Bjarne, Kimonis, Virginia
Publicado 2019

MAPT p.V363I mutation: A rare cause of corticobasal degeneration

por Ahmed, Sarah, Fairen, Monica Diez, Sabir, Marya S., Pastor, Pau, Ding, Jinhui, Ispierto, Lourdes, Butala, Ankur, Morris, Christopher M., Schulte, Claudia, Gasser, Thomas, Jabbari, Edwin, Pletnikova, Olga, Morris, Huw R., Troncoso, Juan, Gelpi, Ellen, Pantelyat, Alexander, Scholz, Sonja W.
Publicado 2019

Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features

por Ziaei, Amin, Xu, Xiaohong, Dehghani, Leila, Bonnard, Carine, Zellner, Andreas, Jin Ng, Alvin Yu, Tohari, Sumanty, Venkatesh, Byrappa, Haffner, Christof, Reversade, Bruno, Shaygannejad, Vahid, Pouladi, Mahmoud A.
Publicado 2019

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts

por Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Liu, Ganqiang, Maple-Grødem, Jodi, Corvol, Jean-Christophe, Pihlstrøm, Lasse, van Nimwegen, Marlies, Hutten, Samantha J., Nguyen, Khanh-Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Day-Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole-Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams-Gray, Caroline H., van de Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.
Publicado 2019

Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease

por Young, Juan I., Sivasankaran, Sathesh K., Wang, Lily, Ali, Aleena, Mehta, Arpit, Davis, David A., Dykxhoorn, Derek M., Petito, Carol K., Beecham, Gary W., Martin, Eden R., Mash, Deborah C., Pericak-Vance, Margaret, Scott, William K., Montine, Thomas J., Vance, Jeffery M.
Publicado 2019

Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy

por Quadir, Asfia, Pontifex, Carly Sabine, Lee Robertson, Helen, Labos, Christopher, Pfeffer, Gerald
Publicado 2019

Opportunities and challenges for junior investigators conducting pain clinical trials

por Adams, Meredith C.B., Bicket, Mark C., Murphy, Jamie D., Wu, Christopher L., Hurley, Robert W.
Publicado 2018

The need for diversity in research on facial expressions of pain

por Dildine, Troy C., Atlas, Lauren Y.
Publicado 2019