Relationship Between Pain Alleviation and Disease-specific Health-related Quality of Life Measures in Patients With Chronic Low Back Pain Receiving Duloxetine: Exploratory Post Hoc...

por Enomoto, Hiroyuki, Sasaki, Nao, Fujikoshi, Shinji, Yoshikawa, Aki, Tsuji, Toshinaga, Takeshita, Katsushi
Publicado 2019

Incidence of Corrective Procedures After Nonoperatively Managed Distal Radius Fractures in the Elderly

por Satariano, Nicholas P., Lalchandani, Gopal R., Menchaca, Sarah E., Immerman, Igor
Publicado 2019

Clinical Features of Thoracic Myelopathy: A Single-Center Study

por Ando, Kei, Imagama, Shiro, Kobayashi, Kazuyoshi, Ito, Kenyu, Tsushima, Mikito, Morozumi, Masayoshi, Tanaka, Satoshi, Machino, Masaaki, Ota, Kyotaro, Nakashima, Hiroaki, Nishida, Yoshihiro, Ishiguro, Naoki
Publicado 2019

Juxta-articular Myxoma of the Hip: A Rare Pediatric Tumor

por Raffaele, Alessandro, Goruppi, Ilaria, Mosconi, Mario, Pelillo, Francesco, Lucioni, Marco, Benazzo, Francesco, Avolio, Luigi
Publicado 2019

Thyrotoxic Periodic Paralysis: A Spine Consultation

por Mease, Samuel J., Faloon, Michael J., Dunn, Conor J., Changoor, Stuart, Sahai, Nikhil, Hussain, Awais K, Emami, Arash
Publicado 2019

A Retrospective Study Comparing a Patient-specific Design Total Knee Arthroplasty With an Off-the-Shelf Design: Unexpected Catastrophic Failure Seen in the Early Patient-specific D...

por Meheux, Carlos J., Park, Kwan J., Clyburn, Terry A.
Publicado 2019

Screening for HIV-Associated Neurocognitive Impairment: Relevance of Psychological Factors and Era of Commencement of Antiretroviral Therapy

por Herrmann, Susan, McKinnon, Elizabeth, Skinner, Matthew, Duracinsky, Martin, Chaney, Richard, Locke, Vance, Mastaglia, Francis
Publicado 2019

Technical Obstacles in Total Knee Arthroplasty Learning: A Steps Breakdown Evaluation

por Harper, Katharine D., Brown, Landon D., Lambert, Bradley S., Clyburn, Terry A., Incavo, Stephen J.
Publicado 2019

The Effect of Metal Instrumentation on Patient and Surgical Team Scatter Radiation Exposure Using Mini C-Arm in a Simulated Forearm Fracture Fixation Model

por Groover, Michael T., Hinkley, Jacob R., Gerow, Daniel E., Bamberger, H. Brent, Evans, Jennifer, Gazaille, Roland E.
Publicado 2019

Influence of Gastric Emptying and Gut Transit Testing on Clinical Management Decisions in Suspected Gastroparesis

por Hasler, William L., Rao, Satish S. C., McCallum, Richard W., Krause, Richard A., Nguyen, Linda A., Schulman, Michael I., Lee, Allen A., Moshiree, Baharak, Wo, John M., Parkman, Henry P., Sarosiek, Irene, Wilding, Gregory E., Kuo, Braden
Publicado 2019

Identification of Epigenetic Methylation Signatures With Clinical Value in Crohn's Disease

por Moret-Tatay, Inés, Cerrillo, Elena, Sáez-González, Esteban, Hervás, David, Iborra, Marisa, Sandoval, Juan, Busó, Enrique, Tortosa, Luis, Nos, Pilar, Beltrán, Belén
Publicado 2019

Identification of a Novel Candidate Gene for Serrated Polyposis Syndrome Germline Predisposition by Performing Linkage Analysis Combined With Whole-Exome Sequencing

por Toma, Claudio, Díaz-Gay, Marcos, Soares de Lima, Yasmin, Arnau-Collell, Coral, Franch-Expósito, Sebastià, Muñoz, Jenifer, Overs, Bronwyn, Bonjoch, Laia, Carballal, Sabela, Ocaña, Teresa, Cuatrecasas, Miriam, Díaz de Bustamante, Aránzazu, Castells, Antoni, Bujanda, Luis, Cubiella, Joaquín, Balaguer, Francesc, Rodríguez-Alcalde, Daniel, Fullerton, Janice M., Castellví-Bel, Sergi
Publicado 2019

Rating scales for rare neurological diseases: What are we learning from Friedreich ataxia?

por Pandolfo, Massimo
Publicado 2019

Psychometric properties of the Friedreich Ataxia Rating Scale

por Rummey, Christian, Corben, Louise A., Delatycki, Martin B., Subramony, S.H., Bushara, Khalaf, Gomez, Christopher M., Hoyle, Joseph Chad, Yoon, Grace, Ravina, Bernard, Mathews, Katherine D., Wilmot, George, Zesiewicz, Theresa, Perlman, Susan, Farmer, Jennifer M., Lynch, David R.
Publicado 2019

Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS

por Amador, Maria-Del-Mar, Muratet, François, Teyssou, Elisa, Banneau, Guillaume, Danel-Brunaud, Véronique, Allart, Etienne, Antoine, Jean-Christophe, Camdessanché, Jean-Philippe, Anheim, Mathieu, Rudolf, Gabrielle, Tranchant, Christine, Fleury, Marie-Céline, Bernard, Emilien, Stevanin, Giovanni, Millecamps, Stéphanie
Publicado 2019

Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders

por Wassman, E. Robert, Ho, Karen S., Bertrand, Diana, Davis, Kyle W., Martin, Megan M., Page, Stephanie, Peiffer, Andreas, Prasad, Aparna, Serrano, Moises A., Twede, Hope, Vanzo, Rena, Scherer, Stephen W., Uddin, Mohammed, Hensel, Charles H.
Publicado 2019

Defining and expanding the phenotype of QARS-associated developmental epileptic encephalopathy

por Johannesen, Katrine M., Mitter, Diana, Janowski, Robert, Roth, Christian, Toulouse, Joseph, Poulat, Anne-Lise, Ville, Dorothee M., Chatron, Nicolas, Brilstra, Eva, Geleijns, Karin, Born, Alfred Peter, McLean, Scott, Nugent, Kimberly, Baynam, Gareth, Poulton, Cathryn, Dreyer, Lauren, Gration, Dylan, Schulz, Solveig, Dieckmann, Andrea, Helbig, Katherine L., Merkenschlager, Andreas, Jamra, Rami, Finck, Anja, Gardella, Elena, Hjalgrim, Helle, Mirzaa, Ghayda, Brancati, Francesco, Bierhals, Tatjana, Denecke, Jonas, Hempel, Maja, Lemke, Johannes R., Rubboli, Guido, Muschke, Petra, Guerrini, Renzo, Vetro, Annalisa, Niessing, Dierk, Lesca, Gaetan, Møller, Rikke S.
Publicado 2019

Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants

por Gauquelin, Laurence, Cayami, Ferdy K., Sztriha, László, Yoon, Grace, Tran, Luan T., Guerrero, Kether, Hocke, François, van Spaendonk, Rosalina M.L., Fung, Eva L., D'Arrigo, Stefano, Vasco, Gessica, Thiffault, Isabelle, Niyazov, Dmitriy M., Person, Richard, Lewis, Kara Stuart, Wassmer, Evangeline, Prescott, Trine, Fallon, Penny, McEntagart, Meriel, Rankin, Julia, Webster, Richard, Philippi, Heike, van de Warrenburg, Bart, Timmann, Dagmar, Dixit, Abhijit, Searle, Claire, Thakur, Nivedita, Kruer, Michael C., Sharma, Suvasini, Vanderver, Adeline, Tonduti, Davide, van der Knaap, Marjo S., Bertini, Enrico, Goizet, Cyril, Fribourg, Sébastien, Wolf, Nicole I., Bernard, Geneviève
Publicado 2019

Cerebral small vessel disease due to a unique heterozygous HTRA1 mutation in an African man

por Oluwole, Olusegun John, Ibrahim, Heba, Garozzo, Debora, Ben Hamouda, Karim, Ismail Mostafa Hassan, Saly, Hegazy, Ahmed Metwaly, Msaddi, Abdul Karim
Publicado 2019

Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation

por Tüngler, Victoria, Doebler-Neumann, Marion, Salandin, Michaela, Kaufmann, Peter, Wolf, Christine, Lucas, Nadja, Harmuth, Florian, Reichbauer, Jennifer, Krägeloh-Mann, Ingeborg, Schüle, Rebecca, Lee-Kirsch, Min Ae
Publicado 2019