Publicaciones científicas

Schiava M, Amos R, VanRuiten H, McDermott MP, Martens WB, Gregory S, Mayhew A, McColl E, Tawil R, Willis T, Bushby K, Griggs RC, Guglieri M; FOR-DMD Investigators of the Muscle Study Group.

Año publicación:

2022

Número de revista:

Neurology vol. 98 n. 4

https://n.neurology.org/content/98/4/e390

Artículo

Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.

Autor/es:

Méreaux JL, Banneau G, Papin M, Coarelli G, Valter R, Raymond L, Kol B, Ariste O, Parodi L, Tissier L, Mairey M, Ait Said S, Gautier C, Guillaud-Bataille M; French SPATAX clinical network, Forlani S, de la Grange P, Brice A, Vazza G, Durr A, Leguern E, Stevanin G.

Editor's Choice

Año publicación:

2022

Número de revista:

Brain vol. 145 n. 3

https://academic.oup.com/brain/article/145/3/1029/6497016

Clinical and genetic spectrum of 355 Chinese children with epilepsy: a trio-sequencing-based study.

Autor/es:

Duan J, Ye Y, Cao D, Zou D, Lu X, Chen L, Wen J, Zou H, Gao J, Li B, Hu Z, Liao J.

Letters to the editor

Año publicación:

2022

Número de revista:

Brain vol. 145 n. 5

https://academic.oup.com/brain/article/145/5/e43/6540466

Artículo

Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.

Autor/es:

Alonso-Pérez J, González-Quereda L, Bruno C, Panicucci C, Alavi A, Nafissi S, Nilipour Y, Zanoteli E, Isihi LMA, Melegh B, Hadzsiev K, Muelas N, Vílchez JJ, Dourado ME, Kadem N, Kutluk G, Umair M, Younus M, Pegorano E, Bello L, Crawford TO, Suárez-Calvet X, Töpf A, Guglieri M, Marini-Bettolo C,...

Editor's Choice

Año publicación:

2022

Número de revista:

Brain vol. 145 n. 2

https://academic.oup.com/brain/article/145/2/596/6369509

Artículo

Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy.

Autor/es:

Martín-Aguilar L, Lleixà C, Pascual-Goñi E, Caballero-Ávila M, Martínez-Martínez L, Díaz-Manera J, Rojas-García R, Cortés-Vicente E, Turon-Sans J, de Luna N, Suárez-Calvet X, Gallardo E, Rajabally Y, Scotton S, Jacobs BC, Baars A, Cortese A, Vegezzi E, Höftberger R, Zimprich F, Roesler C, Nobile-...

Año publicación:

2022

Número de revista:

Neurology Neuroimmunology & Neuroinflammation vol. 9 n. 1

https://nn.neurology.org/content/9/1/e1098

Artículo

Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis.

Autor/es:

Calvo A, Canosa A, Moglia C, Manera U, Grassano M, Vasta R, Palumbo F, Cugnasco P, Gallone S, Brunetti M, De Marchi F, Arena V, Pagani M, Dalgard C, Scholz SW, Chia R, Corrado L, Dalfonso S, Mazzini L, Traynor BJ, Chio A.

Año publicación:

2022

Número de revista:

Neurology® Genetics. vol. 8 n. 6

https://ng.neurology.org/content/8/6/e200033

Artículo

Clinical and neuroscience evidence supports the critical importance of patient expectations and agency in opioid tapering.

Autor/es:

Darnall BD, Fields HL.

Perspective

Año publicación:

2022

Número de revista:

Pain vol. 163 n. 5

https://journals.lww.com/pain/Fulltext/2022/05000/Clinical_and_neuroscience_evid…

Artículo

Clinical and Structural Findings in Patients With Lesion-Induced Dystonia: Descriptive and Quantitative Analysis of Published Cases.

Autor/es:

Corp DT, Greenwood CJ, Morrison-Ham J, Pullinen J, McDowall GM, Younger EFP, Jinnah HA, Fox MD, Joutsa J.

Año publicación:

2022

Número de revista:

Neurology vol. 99 n. 18

https://n.neurology.org/content/99/18/e1957

Una iniciativa de:

Buscador

Clinical and economic burden of prescribing tramadol and other opioids for patients with osteoarthritis in a commercially insured population in the United States.

Clinical and Ergonomic Comparison Between a Robotic Assisted Transfer Device and a Mobile Floor Lift During Caregiver-Assisted Wheelchair Transfers.

Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular Dystrophy.

Clinical and genetic spectra of 1550 index patients with hereditary spastic paraplegia.

Clinical and genetic spectrum of 355 Chinese children with epilepsy: a trio-sequencing-based study.

Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.

Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy.

Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis.

Clinical and neuroscience evidence supports the critical importance of patient expectations and agency in opioid tapering.

Clinical and Structural Findings in Patients With Lesion-Induced Dystonia: Descriptive and Quantitative Analysis of Published Cases.

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