Acute Liver Failure in a Patient With Dengue Shock Syndrome

por Lewis, Justin, Mitra, Arnab, Chang, Michael
Publicado 2020

Pediatric Patient With Ulcerative Colitis-Associated Bronchiectasis

por Russi, Abigail, Gurbani, Neepa, Rosen, Michael J., Mallon, Daniel, LeBlanc, Francis R.
Publicado 2020

Obliterative Muscularization of the Small Bowel Submucosa in Fibrostenotic Crohn's Disease

por McNeill, Matthew B., Suarez, Yvelisse, Axelrad, Jordan
Publicado 2020

Perforated Hemocholecyst: An Unintended Consequence of Endoscopic Variceal Ligation?

por Gasser, Mary C., Sadowski, Brett W., Baird, Dean E., Kwok, Ryan M.
Publicado 2020

2019 PEER REVIEWER RECOGNITION

Publicado 2020

Pathophysiology, Diagnosis, and Treatment of Colonic Gallstone Ileus in an Elderly Patient

por Laxague, Francisco, Ramos, Paula M., Zanfardini, Andrés, Schlottmann, Francisco
Publicado 2020

Dysphagia as a Presentation of Celiac Disease

por Lee, Ada, Tobin, Michelle, Cherian, Julie, Chawla, Anupama
Publicado 2020

Russell Body Barrett's Esophagus

por Dhorajiya, Pooja, Mannan, Rifat
Publicado 2020

Esophageal Bronchial Artery Fistulaization: A Complication of an Endobronchial Ultrasound

por Jadeja, Sonal, Green, Kevin, Shuja, Asim, Malespin, Miguel, De Melo, Silvio
Publicado 2020

Use of Fecal Microbial Transplantation for Immune Checkpoint Inhibitor Colitis

por Fasanello, Micaela K., Robillard, Kevin T., Boland, Patrick M., Bain, Andrew J., Kanehira, Kazunori
Publicado 2020

Bleeding From Buried Cholecystogastrostomy Lumen-Apposing Metal Stent: The Double Pigtail Catheter Rescue Treatment

por Sánchez-Luna, Sergio A., Wong, Morgan, Rustagi, Tarun
Publicado 2020

Ulcerative Proctitis in a Patient With a History of Fecal Microbiota Transplant for Clostridioides difficile Infection

por Massaro, Michael, Vansia, Jhanvi, McGill, Sarah
Publicado 2020

HSV-1 Ulcers as an Infrequent Cause of Hematochezia

por Ahmed, Zarir, Narayanan, Mechu, Hachem, Christine
Publicado 2020

Hepatic Steatosis Resulting From LMNA-Associated Familial Lipodystrophy

por Mahdi, Layth, Kahn, Allon, Dhamija, Radhika, Vargas, Hugo E.
Publicado 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy revisited: Genotype-phenotype correlations of all published cases

por Xiromerisiou, Georgia, Marogianni, Chrysoula, Dadouli, Katerina, Zompola, Christina, Georgouli, Despoina, Provatas, Antonios, Theodorou, Aikaterini, Zervas, Paschalis, Nikolaidou, Christina, Stergiou, Stergios, Ntellas, Panagiotis, Sokratous, Maria, Stathis, Pantelis, Paraskevas, Georgios P., Bonakis, Anastasios, Voumvourakis, Konstantinos, Hadjichristodoulou, Christos, Hadjigeorgiou, Georgios M., Tsivgoulis, Georgios
Publicado 2020

Expanding the phenotypic and molecular spectrum of RNA polymerase III–related leukodystrophy

por Perrier, Stefanie, Gauquelin, Laurence, Fallet-Bianco, Catherine, Dishop, Megan K., Michell-Robinson, Mackenzie A., Tran, Luan T., Guerrero, Kether, Darbelli, Lama, Srour, Myriam, Petrecca, Kevin, Renaud, Deborah L., Saito, Michael, Cohen, Seth, Leiz, Steffen, Alhaddad, Bader, Haack, Tobias B., Tejera-Martin, Ingrid, Monton, Fernando I., Rodriguez-Espinosa, Norberto, Pohl, Daniela, Nageswaran, Savithri, Grefe, Annette, Glamuzina, Emma, Bernard, Geneviève
Publicado 2020

Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington disease

por Claassen, Daniel O., Corey-Bloom, Jody, Dorsey, E. Ray, Edmondson, Mary, Kostyk, Sandra K., LeDoux, Mark S., Reilmann, Ralf, Rosas, H. Diana, Walker, Francis, Wheelock, Vicki, Svrzikapa, Nenad, Longo, Kenneth A., Goyal, Jaya, Hung, Serena, Panzara, Michael A.
Publicado 2020

Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

por Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Leruez, Stéphanie, Colin, Estelle, Meunier, Audrey, Vignal, Catherine, Smirnov, Vasily, Defoort-Dhellemmes, Sabine, Drumare Bouvet, Isabelle, Goizet, Cyril, Votruba, Marcela, Jurkute, Neringa, Yu-Wai-Man, Patrick, Tagliavini, Francesca, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Procaccio, Vincent, Zanlonghi, Xavier, Meunier, Isabelle, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy
Publicado 2020

Intronic pentanucleotide expansion in the replication factor 1 gene (RFC1) is a major cause of adult-onset ataxia

por Boesch, Sylvia M., Nance, Martha A.
Publicado 2020

Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation

por Yasuda, Rei, Yoshida, Tomokatsu, Mizuta, Ikuko, Watanabe, Masashi, Nakano, Masakazu, Sato, Ryuichi, Tokuda, Yuichi, Omi, Natsue, Sakai, Norio, Nakagawa, Masanori, Tashiro, Kei, Mizuno, Toshiki
Publicado 2020