Una iniciativa de:

Fundació Guttmann
Institut Guttmann

Anuncia't

Cercador

Publicacions científiques

  • proyecto que busca voluntarios con discapacidad
Article

Hemorrhagic cerebral small vessel disease caused by a novel mutation in 3′ UTR of collagen type IV alpha 1

Autor/s: 
Sakai N, Uemura M, Kato T, Nozaki H, Koyama A, Ando S, Kamei H, Kato M, Onodera O.
Clinical/Scientific Notes
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 1
https://ng.neurology.org/content/6/1/e383
Article

Hereditary cerebral amyloid angiopathy, Piedmont-type mutation.

Autor/s: 
Kozberg MG, van Veluw SJ, Frosch MP, Greenberg SM.
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 2
https://ng.neurology.org/content/6/2/e411
Article

Heritability of cervical spinal cord structure.

Autor/s: 
Solstrand Dahlberg L, Viessmann O, Linnman C.
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 2
https://ng.neurology.org/content/6/2/e401
Article

Herpes simplex virus 2 encephalitis in a patient heterozygous for a TLR3 mutation.

Autor/s: 
Hautala T, Chen J, Tervonen L, Partanen T, Winqvist S, Lehtonen J, Saarela J, Kraatari M, Kuismin O, Vuorinen T, Glumoff V, Åström P, Huuskonen U, Lorenzo L, Casanova JL, Zhang SY, Seppänen MRJ. ...
Clinical/Scientific Notes
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 6
https://ng.neurology.org/content/6/6/e532
Article

Herpes zoster lumbar radiculitis.

Autor/s: 
Changa AR, Jain R.
NeuroImages
Any publicació: 
2020
Número de revista: 
Neurology vol. 95 n. 12
https://n.neurology.org/content/95/12/552
Article

Heterogeneity in Temporal Ordering of Depression and Participation After Traumatic Brain Injury.

Autor/s: 
Rabinowitz AR, Chervoneva I, Hart T, O'Neil-Pirozzi TM, Juengst SB, Hoffman JM...
Any publicació: 
2020
Número de revista: 
Archives of Physical Medicine and Rehabilitation. vol. 101 n. 11
https://www.archives-pmr.org/article/S0003-9993(20)30419-6/fulltext
Article

Heterozygous STUB1 missense variants cause ataxia, cognitive decline, and STUB1 mislocalization.

Autor/s: 
Chen DH, Latimer C, Yagi M, Ndugga-Kabuye MK, Heigham E, Jayadev S, Meabon JS, Gomez CM, Keene CD, Cook DG, Raskind WH, Bird TD. ...
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 2
https://ng.neurology.org/content/6/2/e397
Article

Heterozygous variants in DCC: Beyond congenital mirror movements.

Autor/s: 
Thams S, Islam M, Lindefeldt M, Nordgren A, Granberg T, Tesi B, Barbany G, Nilsson D, Paucar M.
Any publicació: 
2020
Número de revista: 
Neurology® Genetics. vol. 6 n. 6
https://ng.neurology.org/content/6/6/e526
Article

High incidence and prevalence of MS in Møre and Romsdal County, Norway, 1950-2018.

Autor/s: 
Willumsen JS, Aarseth JH, Myhr KM, Midgard R.
Any publicació: 
2020
Número de revista: 
Neurology Neuroimmunology & Neuroinflammation vol. 7 n. 3
https://nn.neurology.org/content/7/3/e713
Article

High proportion of Guillain-Barré syndrome associated with chikungunya in Northeast Brazil

Autor/s: 
Matos AMB, Maia Carvalho FM, Malta DL, Rodrigues CL, Félix AC, Pannuti CS, Lima ADDR, Espósito DLA, Dos Santos LMB, von Glehn F, Colares JKB, da Fonseca BAL, de Oliveira ACP, Romano CM.
Clinical/Scientific Notes
Any publicació: 
2020
Número de revista: 
Neurology Neuroimmunology & Neuroinflammation vol. 7 n. 5
https://nn.neurology.org/content/7/5/e833

Trobes a faltar informació? Fes-nos arribar els teus suggeriments!

Ajuda'ns a millorar!