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51-60 trong số 145 kết quả
SIMPATHIC: Accelerating drug repurposing for rare diseases by exploiting SIMilarities in clinical and molecular PATHology
Tác giả: Clara D M van Karnebeek, Annelieke R Müller, Kit C B Roes, Anna Sanchez, Raymond Schipper, Mark D Wilkinson, Peter A C 't Hoen, Laura Benkemoun, Ibrahim Boussaad, Martina C Cornel, Joanna IntHout, Martin de Kort, Sofia de Oliveira Martins, Alessandro Prigione, Tessel Rigter
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc:  629.4582
 
Argentine program of home infusions with enzyme replacement therapy for lysosomal diseases: Results in safety, quality o...
Tác giả: Guillermo Drelichman, Juan M Politei, María Larroude, Gabriel Aguilar, Paola Reichel, Alberto Dubrovsky, Gustavo Cabrera, Adriana Arizo, Marcela Corrales, Adriana Degano, Alejandro Faimboin, Analía Carvani, Nicolás Fernandez Escobar, Fernando Gómez Pizarro, Fernando Perretta, Barbara Soberón, Nora Basack, Norberto Guelbert, Nora Watman, Norberto Antongiovanni, Fernanda Cuello, Gerardo Mogni
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 
Improving acute care for Primary Mitochondrial Disease: Development of a publicly available clinical care pathway
Tác giả: Matthew M Demczko, Bridget Blowey, Rebecca D Ganetzky, Amy Goldstein, Brandon C Ku, Jane Lavelle, Cassandra Tormey
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 
Untargeted metabolomics analysis as a potential screening tool for 3-methylglutaconic aciduria syndromes
Tác giả: Charles R DiFalco, Hongzheng Dai, Sarah H Elsea, Lisa Emrick, Charul Gijavanekar, Alexandra N Grace, Ning Liu, Keren Machol, Laura Mackay, Elizabeth Mizerik, Fernando Scaglia, Liesbeth Vossaert, Yue Wang, Fan Xia
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 
Genetic analysis and multimodal imaging confirm m.12148 T > C mitochondrial variant pathogenicity leading to multisys...
Tác giả: Kinsley Belle, Alexander Kreymerman, Richard T Lee, Jamal Nasir, Gregory M Enns, Ioannis Karakikes, Andrew M Schaefer, Robert W Taylor, Mark Mercola, Dwight Koeberl, Edward H Wood, Jill L Young, Nirmal Vadgama, Marco H Ji, Sandeep Randhawa, Juan Caicedo, Megan Wong, Stephanie P Muscat, Casey A Gifford
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc:  321.05
 
The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy
Tác giả: Francesco Gavazzi, Brittany Charsar, Kayla Muirhead, Asako Takanohashi, Joshua L Bonkowsky, Kelsee Meyerhoffer, Cas Simons, Hiroshi Doi, Miyatake Satoko, Naomichi Matsumoto, Mauricio R Delgado, Meredith Sanchez-Castillo, Eline Hamilton, Jingming Wang, Daniel Rocha de Carvalho, Ivailo Tournev, Teodora Chamova, Albena Jordanova, Nancy J Clegg, Francesco Nicita, Enrico Bertini, Michelle Teng, Dan Williams, Jacqueline A Erler, Davide Tonduti, Henry Houlden, Menno Stellingwerff, Evangeline Wassmer, Angeles Garcia-Cazorla, Geneviève Bernard, Amytice Mirchi, Helia Toutounchi, Nicole I Wolf, Marjo S van der Knaap, Virali Patel, Justine Shults, Laura A Adang, Adeline L Vanderver, Sarah Woidill, Anjana Sevagamoorthy, Guy Helman, Johanna Schmidt, Amy Pizzino
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc:  271.6
 
Kidney involvement in glycogen storage disease type I: Current knowledge and key challenges
Tác giả: Anke Schumann, Sven F Garbade, Eva Thimm, Natalie Weinhold, Monika Williams, Saskia Wortmann, Sarah C Grünert, Skadi Beblo, Matthias Gautschi, Dorothea Haas, Michel Hochuli, Georg Hoffmann, Petra May, Martin Merkel, Sabine Scholl-Bürgi
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc:  636.0885
 
Rare disorders, big challenges: Special issue on congenital disorders of glycosylation
Tác giả: Peter Witters, Carlos R Ferreira
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 
Exploratory metabolomic profiling of plasma and urine in patients with mucopolysaccharidosis type II (Hunter syndrome): ...
Tác giả: Asma Farjallah, Christiane Auray-Blais, Roberto Giugliani, Bruno Maranda
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 
Comprehensive analysis of GDF15 as a biomarker in primary mitochondrial myopathies
Tác giả: Paloma Martín-Jimenez, Joaquín Arenas, Laura Bermejo-Guerrero, Alberto Blázquez, Cristina Domínguez-González, Rocío Garrido-Moraga, Aurelio Hernández-Laín, Ana Hernández-Voth, David Lora, Miguel Ángel Martín, Montserrat Morales, María Navarro-Riquelme, Pablo Serrano-Lorenzo
Xuất bản: United States: Molecular genetics and metabolism , 2025
Bộ sưu tập: NCBI
ddc: 
 

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